DrTarget’s AI-Powered Insights for Psychiatric Disorders
DrTarget has identified target-disease associations for psychiatric disorders, leveraging data from PubChem, Open Targets and other public repositories. Our AI-driven analytics and machine learning models uncover novel targets and molecular pathways, enabling precision medicine approaches for conditions such as:
✔ Depression
✔ Schizophrenia
✔ Bipolar Disorder
✔ Anxiety Disorders
✔ Neurodevelopmental Conditions
By integrating virtual screening, drug repurposing strategies, and multi-omics validation, we provide deep insights into the molecular mechanisms of psychiatric diseases. Our approach also supports biomarker discovery and novel therapeutic development, bridging the gap between computational predictions and clinical applications.
Check best scored target-disease associations in table:
BioAssay Name | program | diseaseName | assayType | testedCompounds | activeCompounds | associationScore | numberOfEvidences |
---|---|---|---|---|---|---|---|
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | mental or behavioural disorder | targetBased | 363803 | 2412 | 0.674689655936239 | 2309 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | mental or behavioural disorder | targetBased | 108286 | 1415 | 0.551471869587019 | 1571 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | mental or behavioural disorder | targetBased | 359518 | 300 | 0.710887433093737 | 2921 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | mental or behavioural disorder | targetBased | 335652 | 1779 | 0.710887433093737 | 2921 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | mental or behavioural disorder | targetBased | 357537 | 806 | 0.710887433093737 | 2921 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | mental or behavioural disorder | targetBased | 339887 | 1178 | 0.710887433093737 | 2921 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | mental or behavioural disorder | targetBased | 362274 | 1056 | 0.710887433093737 | 2921 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | mental or behavioural disorder | targetBased | 336308 | 6862 | 0.710887433093737 | 2921 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | mental or behavioural disorder | targetBased | 364051 | 9106 | 0.678096812690304 | 635 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | mental or behavioural disorder | targetBased | 407539 | 2380 | 0.678096812690304 | 635 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | mental or behavioural disorder | targetBased | 407539 | 2380 | 0.678096812690304 | 635 |
Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R | MC4R | mental or behavioural disorder | targetBased | 356160 | 3470 | 0.520891499859175 | 39 |
TRFRET-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): antagonists of MC4R | MC4R | mental or behavioural disorder | targetBased | 356160 | 1703 | 0.520891499859175 | 39 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | mental or behavioural disorder | targetBased | 64908 | 366 | 0.636562574634408 | 918 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | mental or behavioural disorder | targetBased | 61606 | 416 | 0.636562574634408 | 918 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | mental or behavioural disorder | targetBased | 339772 | 8480 | 0.569683743699563 | 262 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | post-traumatic stress disorder | targetBased | 363803 | 2412 | 0.642088916127175 | 81 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | post-traumatic stress disorder | targetBased | 335239 | 991 | 0.548657439227214 | 17 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | post-traumatic stress disorder | targetBased | 335239 | 695 | 0.548657439227214 | 17 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | post-traumatic stress disorder | targetBased | 359518 | 300 | 0.645823745379977 | 110 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | post-traumatic stress disorder | targetBased | 335652 | 1779 | 0.645823745379977 | 110 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | post-traumatic stress disorder | targetBased | 357537 | 806 | 0.645823745379977 | 110 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | post-traumatic stress disorder | targetBased | 339887 | 1178 | 0.645823745379977 | 110 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | post-traumatic stress disorder | targetBased | 362274 | 1056 | 0.645823745379977 | 110 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | post-traumatic stress disorder | targetBased | 336308 | 6862 | 0.645823745379977 | 110 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | post-traumatic stress disorder | targetBased | 339297 | 1446 | 0.627147038346792 | 44 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | post-traumatic stress disorder | targetBased | 64908 | 366 | 0.607658019448827 | 59 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | post-traumatic stress disorder | targetBased | 61606 | 416 | 0.607658019448827 | 59 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | cocaine dependence | targetBased | 363803 | 2412 | 0.504413979083123 | 32 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | cocaine dependence | targetBased | 359518 | 300 | 0.515032348421456 | 92 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | cocaine dependence | targetBased | 335652 | 1779 | 0.515032348421456 | 92 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | cocaine dependence | targetBased | 357537 | 806 | 0.515032348421456 | 92 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | cocaine dependence | targetBased | 339887 | 1178 | 0.515032348421456 | 92 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | cocaine dependence | targetBased | 362274 | 1056 | 0.515032348421456 | 92 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | cocaine dependence | targetBased | 336308 | 6862 | 0.515032348421456 | 92 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | aggressive behavior | targetBased | 363803 | 2412 | 0.65723170170587 | 63 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | aggressive behavior | targetBased | 359518 | 300 | 0.65723170170587 | 63 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | aggressive behavior | targetBased | 335652 | 1779 | 0.65723170170587 | 63 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | aggressive behavior | targetBased | 357537 | 806 | 0.65723170170587 | 63 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | aggressive behavior | targetBased | 339887 | 1178 | 0.65723170170587 | 63 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | aggressive behavior | targetBased | 362274 | 1056 | 0.65723170170587 | 63 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | aggressive behavior | targetBased | 336308 | 6862 | 0.65723170170587 | 63 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | nicotine dependence | targetBased | 290355 | 265 | 0.560198005654315 | 29 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | nicotine dependence | targetBased | 335239 | 991 | 0.565774937759867 | 57 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | nicotine dependence | targetBased | 335239 | 695 | 0.565774937759867 | 57 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | nicotine dependence | targetBased | 108286 | 1415 | 0.779304545775545 | 138 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | nicotine dependence | targetBased | 339297 | 1446 | 0.55928325716652 | 8 |
qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | MAPT | Pick disease | pathwayBased | 267412 | 5703 | 0.813029001015443 | 2286 |
qHTS Assay for Tau Filament Binding | MAPT | Pick disease | targetBased | 69668 | 1391 | 0.813029001015443 | 2286 |
qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | MAPT | Pick disease | pathwayBased | 271402 | 1048 | 0.813029001015443 | 2286 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | autism spectrum disorder | targetBased | 363803 | 2412 | 0.589529636394361 | 105 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | autism spectrum disorder | targetBased | 359518 | 300 | 0.701153255351398 | 112 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | autism spectrum disorder | targetBased | 335652 | 1779 | 0.701153255351398 | 112 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | autism spectrum disorder | targetBased | 357537 | 806 | 0.701153255351398 | 112 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | autism spectrum disorder | targetBased | 339887 | 1178 | 0.701153255351398 | 112 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | autism spectrum disorder | targetBased | 362274 | 1056 | 0.701153255351398 | 112 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | autism spectrum disorder | targetBased | 336308 | 6862 | 0.701153255351398 | 112 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | autism spectrum disorder | targetBased | 64908 | 366 | 0.568058344635926 | 30 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | autism spectrum disorder | targetBased | 61606 | 416 | 0.568058344635926 | 30 |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | autism spectrum disorder | targetBased | 324747 | 1043 | 0.543942541384409 | 55 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | sleep apnea | targetBased | 335239 | 991 | 0.591705290314346 | 14 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | sleep apnea | targetBased | 335239 | 695 | 0.591705290314346 | 14 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | autism spectrum disorder | targetBased | 339772 | 8480 | 0.583045313028752 | 21 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | Asperger syndrome | targetBased | 359518 | 300 | 0.506901236061246 | 11 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | Asperger syndrome | targetBased | 335652 | 1779 | 0.506901236061246 | 11 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | Asperger syndrome | targetBased | 357537 | 806 | 0.506901236061246 | 11 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | Asperger syndrome | targetBased | 339887 | 1178 | 0.506901236061246 | 11 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | Asperger syndrome | targetBased | 362274 | 1056 | 0.506901236061246 | 11 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | Asperger syndrome | targetBased | 336308 | 6862 | 0.506901236061246 | 11 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | autism | targetBased | 363803 | 2412 | 0.666809464893294 | 263 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | autism | targetBased | 359518 | 300 | 0.675593943440856 | 261 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | autism | targetBased | 335652 | 1779 | 0.675593943440856 | 261 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | autism | targetBased | 357537 | 806 | 0.675593943440856 | 261 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | autism | targetBased | 339887 | 1178 | 0.675593943440856 | 261 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | autism | targetBased | 362274 | 1056 | 0.675593943440856 | 261 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | autism | targetBased | 336308 | 6862 | 0.675593943440856 | 261 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | autism | targetBased | 64908 | 366 | 0.654787051710058 | 59 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | autism | targetBased | 61606 | 416 | 0.654787051710058 | 59 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | unipolar depression | targetBased | 290355 | 265 | 0.626689907251647 | 26 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | unipolar depression | targetBased | 363803 | 2412 | 0.673413511389257 | 303 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | unipolar depression | targetBased | 335239 | 991 | 0.619197357878222 | 24 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | unipolar depression | targetBased | 335239 | 695 | 0.619197357878222 | 24 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | unipolar depression | targetBased | 86095 | 1114 | 0.502143011397617 | 12 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | unipolar depression | targetBased | 108286 | 1415 | 0.67704520260216 | 473 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | unipolar depression | targetBased | 359518 | 300 | 0.778810435779702 | 148 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | unipolar depression | targetBased | 335652 | 1779 | 0.778810435779702 | 148 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | unipolar depression | targetBased | 357537 | 806 | 0.778810435779702 | 148 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | unipolar depression | targetBased | 339887 | 1178 | 0.778810435779702 | 148 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | unipolar depression | targetBased | 362274 | 1056 | 0.778810435779702 | 148 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | unipolar depression | targetBased | 336308 | 6862 | 0.778810435779702 | 148 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | unipolar depression | targetBased | 364051 | 9106 | 0.652139811175138 | 47 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | unipolar depression | targetBased | 407539 | 2380 | 0.652139811175138 | 47 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | unipolar depression | targetBased | 407539 | 2380 | 0.652139811175138 | 47 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | unipolar depression | targetBased | 64908 | 366 | 0.663206489836322 | 246 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | unipolar depression | targetBased | 61606 | 416 | 0.663206489836322 | 246 |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | unipolar depression | targetBased | 361330 | 3713 | 0.594121772000262 | 11 |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | unipolar depression | targetBased | 57705 | 3413 | 0.594121772000262 | 11 |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | unipolar depression | targetBased | 355805 | 11440 | 0.594121772000262 | 11 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | unipolar depression | targetBased | 339772 | 8480 | 0.628732651518689 | 32 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | attention deficit hyperactivity disorder | targetBased | 290355 | 265 | 0.553383944086691 | 12 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | attention deficit hyperactivity disorder | targetBased | 363803 | 2412 | 0.639130063012709 | 60 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | attention deficit hyperactivity disorder | targetBased | 335239 | 991 | 0.568194468638635 | 19 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | attention deficit hyperactivity disorder | targetBased | 335239 | 695 | 0.568194468638635 | 19 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | attention deficit hyperactivity disorder | targetBased | 108286 | 1415 | 0.709461505766322 | 1824 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | attention deficit hyperactivity disorder | targetBased | 359518 | 300 | 0.721501946320093 | 203 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | attention deficit hyperactivity disorder | targetBased | 335652 | 1779 | 0.721501946320093 | 203 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | attention deficit hyperactivity disorder | targetBased | 357537 | 806 | 0.721501946320093 | 203 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | attention deficit hyperactivity disorder | targetBased | 339887 | 1178 | 0.721501946320093 | 203 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | attention deficit hyperactivity disorder | targetBased | 362274 | 1056 | 0.721501946320093 | 203 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | attention deficit hyperactivity disorder | targetBased | 336308 | 6862 | 0.721501946320093 | 203 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | attention deficit hyperactivity disorder | targetBased | 64908 | 366 | 0.551799572120731 | 32 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | attention deficit hyperactivity disorder | targetBased | 61606 | 416 | 0.551799572120731 | 32 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | drug dependence | targetBased | 290355 | 265 | 0.667078041570145 | 390 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | drug dependence | targetBased | 363803 | 2412 | 0.574467276224984 | 70 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | drug dependence | targetBased | 335239 | 991 | 0.676418660162289 | 657 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | drug dependence | targetBased | 335239 | 695 | 0.676418660162289 | 657 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | drug dependence | targetBased | 108286 | 1415 | 0.643739922579374 | 259 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | drug dependence | targetBased | 359518 | 300 | 0.631827536503145 | 278 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | drug dependence | targetBased | 335652 | 1779 | 0.631827536503145 | 278 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | drug dependence | targetBased | 357537 | 806 | 0.631827536503145 | 278 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | drug dependence | targetBased | 339887 | 1178 | 0.631827536503145 | 278 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | drug dependence | targetBased | 362274 | 1056 | 0.631827536503145 | 278 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | drug dependence | targetBased | 336308 | 6862 | 0.631827536503145 | 278 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | drug dependence | targetBased | 339772 | 8480 | 0.509507133272657 | 51 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | obstructive sleep apnea | targetBased | 335239 | 991 | 0.542693545696731 | 18 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | obstructive sleep apnea | targetBased | 335239 | 695 | 0.542693545696731 | 18 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | obstructive sleep apnea | targetBased | 108286 | 1415 | 0.616870615441254 | 21 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | conduct disorder | targetBased | 363803 | 2412 | 0.580921152944216 | 8 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | conduct disorder | targetBased | 359518 | 300 | 0.595019512773013 | 24 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | conduct disorder | targetBased | 335652 | 1779 | 0.595019512773013 | 24 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | conduct disorder | targetBased | 357537 | 806 | 0.595019512773013 | 24 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | conduct disorder | targetBased | 339887 | 1178 | 0.595019512773013 | 24 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | conduct disorder | targetBased | 362274 | 1056 | 0.595019512773013 | 24 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | conduct disorder | targetBased | 336308 | 6862 | 0.595019512773013 | 24 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | neurotic disorder | targetBased | 359518 | 300 | 0.529577792747223 | 64 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | neurotic disorder | targetBased | 335652 | 1779 | 0.529577792747223 | 64 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | neurotic disorder | targetBased | 357537 | 806 | 0.529577792747223 | 64 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | neurotic disorder | targetBased | 339887 | 1178 | 0.529577792747223 | 64 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | neurotic disorder | targetBased | 362274 | 1056 | 0.529577792747223 | 64 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | neurotic disorder | targetBased | 336308 | 6862 | 0.529577792747223 | 64 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | heroin dependence | targetBased | 290355 | 265 | 0.631779587579708 | 51 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | heroin dependence | targetBased | 335239 | 991 | 0.638960310809911 | 104 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | heroin dependence | targetBased | 335239 | 695 | 0.638960310809911 | 104 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | obsessive-compulsive disorder | targetBased | 363803 | 2412 | 0.614970694532657 | 62 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | obsessive-compulsive disorder | targetBased | 108286 | 1415 | 0.52519332062715 | 39 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | obsessive-compulsive disorder | targetBased | 359518 | 300 | 0.672861113899014 | 39 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | obsessive-compulsive disorder | targetBased | 335652 | 1779 | 0.672861113899014 | 39 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | obsessive-compulsive disorder | targetBased | 357537 | 806 | 0.672861113899014 | 39 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | obsessive-compulsive disorder | targetBased | 339887 | 1178 | 0.672861113899014 | 39 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | obsessive-compulsive disorder | targetBased | 362274 | 1056 | 0.672861113899014 | 39 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | obsessive-compulsive disorder | targetBased | 336308 | 6862 | 0.672861113899014 | 39 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | panic disorder | targetBased | 363803 | 2412 | 0.511722812322968 | 23 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | panic disorder | targetBased | 359518 | 300 | 0.509506968390538 | 11 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | panic disorder | targetBased | 335652 | 1779 | 0.509506968390538 | 11 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | panic disorder | targetBased | 357537 | 806 | 0.509506968390538 | 11 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | panic disorder | targetBased | 339887 | 1178 | 0.509506968390538 | 11 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | panic disorder | targetBased | 362274 | 1056 | 0.509506968390538 | 11 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | panic disorder | targetBased | 336308 | 6862 | 0.509506968390538 | 11 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | mood disorder | targetBased | 363803 | 2412 | 0.59091958364141 | 767 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | mood disorder | targetBased | 108286 | 1415 | 0.574924572650151 | 332 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | mood disorder | targetBased | 359518 | 300 | 0.6712322106451 | 702 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | mood disorder | targetBased | 335652 | 1779 | 0.6712322106451 | 702 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | mood disorder | targetBased | 357537 | 806 | 0.6712322106451 | 702 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | mood disorder | targetBased | 339887 | 1178 | 0.6712322106451 | 702 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | mood disorder | targetBased | 362274 | 1056 | 0.6712322106451 | 702 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | mood disorder | targetBased | 336308 | 6862 | 0.6712322106451 | 702 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | gambling behaviour | targetBased | 290355 | 265 | 0.500222256227568 | 15 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | gambling behaviour | targetBased | 335239 | 991 | 0.500222256227568 | 15 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | gambling behaviour | targetBased | 335239 | 695 | 0.500222256227568 | 15 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | methamphetamine dependence | targetBased | 363803 | 2412 | 0.598875408626687 | 20 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | methamphetamine dependence | targetBased | 108286 | 1415 | 0.586268551754346 | 48 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | methamphetamine dependence | targetBased | 359518 | 300 | 0.599218832228455 | 20 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | methamphetamine dependence | targetBased | 335652 | 1779 | 0.599218832228455 | 20 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | methamphetamine dependence | targetBased | 357537 | 806 | 0.599218832228455 | 20 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | methamphetamine dependence | targetBased | 339887 | 1178 | 0.599218832228455 | 20 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | methamphetamine dependence | targetBased | 362274 | 1056 | 0.599218832228455 | 20 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | methamphetamine dependence | targetBased | 336308 | 6862 | 0.599218832228455 | 20 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | Tourette syndrome | targetBased | 363803 | 2412 | 0.650624549944278 | 33 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | Tourette syndrome | targetBased | 359518 | 300 | 0.710541683908988 | 86 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | Tourette syndrome | targetBased | 335652 | 1779 | 0.710541683908988 | 86 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | Tourette syndrome | targetBased | 357537 | 806 | 0.710541683908988 | 86 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | Tourette syndrome | targetBased | 339887 | 1178 | 0.710541683908988 | 86 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | Tourette syndrome | targetBased | 362274 | 1056 | 0.710541683908988 | 86 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | Tourette syndrome | targetBased | 336308 | 6862 | 0.710541683908988 | 86 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | Tourette syndrome | targetBased | 364051 | 9106 | 0.588857175513129 | 17 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | Tourette syndrome | targetBased | 407539 | 2380 | 0.588857175513129 | 17 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | Tourette syndrome | targetBased | 407539 | 2380 | 0.588857175513129 | 17 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | Tourette syndrome | targetBased | 64908 | 366 | 0.60757010167286 | 18 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | Tourette syndrome | targetBased | 61606 | 416 | 0.60757010167286 | 18 |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | Tourette syndrome | targetBased | 361330 | 3713 | 0.528076886310531 | 23 |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | Tourette syndrome | targetBased | 57705 | 3413 | 0.528076886310531 | 23 |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | Tourette syndrome | targetBased | 355805 | 11440 | 0.528076886310531 | 23 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | insomnia | targetBased | 363803 | 2412 | 0.618331153675178 | 56 |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | insomnia | targetBased | 326024 | 5748 | 0.648644519344265 | 89 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | insomnia | targetBased | 326024 | 1387 | 0.648644519344265 | 89 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | insomnia | targetBased | 108286 | 1415 | 0.523021843492775 | 12 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | eating disorder | targetBased | 363803 | 2412 | 0.565476040057905 | 31 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | eating disorder | targetBased | 108286 | 1415 | 0.589793920351293 | 42 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | eating disorder | targetBased | 359518 | 300 | 0.604372553853475 | 38 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | eating disorder | targetBased | 335652 | 1779 | 0.604372553853475 | 38 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | eating disorder | targetBased | 357537 | 806 | 0.604372553853475 | 38 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | eating disorder | targetBased | 339887 | 1178 | 0.604372553853475 | 38 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | eating disorder | targetBased | 362274 | 1056 | 0.604372553853475 | 38 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | eating disorder | targetBased | 336308 | 6862 | 0.604372553853475 | 38 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | eating disorder | targetBased | 364051 | 9106 | 0.531818103244732 | 10 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | eating disorder | targetBased | 407539 | 2380 | 0.531818103244732 | 10 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | eating disorder | targetBased | 407539 | 2380 | 0.531818103244732 | 10 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | opioid dependence | targetBased | 290355 | 265 | 0.667574265772021 | 380 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | opioid dependence | targetBased | 335239 | 991 | 0.67511318074411 | 666 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | opioid dependence | targetBased | 335239 | 695 | 0.67511318074411 | 666 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | opioid dependence | targetBased | 359518 | 300 | 0.586603345912258 | 54 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | opioid dependence | targetBased | 335652 | 1779 | 0.586603345912258 | 54 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | opioid dependence | targetBased | 357537 | 806 | 0.586603345912258 | 54 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | opioid dependence | targetBased | 339887 | 1178 | 0.586603345912258 | 54 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | opioid dependence | targetBased | 362274 | 1056 | 0.586603345912258 | 54 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | opioid dependence | targetBased | 336308 | 6862 | 0.586603345912258 | 54 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | opioid dependence | targetBased | 316642 | 617 | 0.577905333654408 | 10 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | opioid dependence | targetBased | 339772 | 8480 | 0.518667722386517 | 13 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | anxiety | targetBased | 363803 | 2412 | 0.630433271106812 | 260 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | psychosis | targetBased | 363803 | 2412 | 0.676238391345276 | 1279 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | psychosis | targetBased | 359518 | 300 | 0.717504452857608 | 1775 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | psychosis | targetBased | 335652 | 1779 | 0.717504452857608 | 1775 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | psychosis | targetBased | 357537 | 806 | 0.717504452857608 | 1775 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | psychosis | targetBased | 339887 | 1178 | 0.717504452857608 | 1775 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | psychosis | targetBased | 362274 | 1056 | 0.717504452857608 | 1775 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | psychosis | targetBased | 336308 | 6862 | 0.717504452857608 | 1775 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | psychosis | targetBased | 364051 | 9106 | 0.690741306707689 | 392 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | psychosis | targetBased | 407539 | 2380 | 0.690741306707689 | 392 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | psychosis | targetBased | 407539 | 2380 | 0.690741306707689 | 392 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | psychosis | targetBased | 64908 | 366 | 0.642439139861967 | 296 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | psychosis | targetBased | 61606 | 416 | 0.642439139861967 | 296 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | anxiety | targetBased | 359518 | 300 | 0.633822468610396 | 248 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | anxiety | targetBased | 335652 | 1779 | 0.633822468610396 | 248 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | anxiety | targetBased | 357537 | 806 | 0.633822468610396 | 248 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | anxiety | targetBased | 339887 | 1178 | 0.633822468610396 | 248 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | anxiety | targetBased | 362274 | 1056 | 0.633822468610396 | 248 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | anxiety | targetBased | 336308 | 6862 | 0.633822468610396 | 248 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | anxiety | targetBased | 64908 | 366 | 0.633991676701545 | 936 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | anxiety | targetBased | 61606 | 416 | 0.633991676701545 | 936 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | anxiety | targetBased | 339772 | 8480 | 0.526319275317686 | 9 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | schizoaffective disorder | targetBased | 363803 | 2412 | 0.664704658955117 | 297 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | schizoaffective disorder | targetBased | 86095 | 1114 | 0.611730200008939 | 12 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | schizoaffective disorder | targetBased | 108286 | 1415 | 0.578791172578599 | 8 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | schizoaffective disorder | targetBased | 359518 | 300 | 0.665187702963058 | 315 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | schizoaffective disorder | targetBased | 335652 | 1779 | 0.665187702963058 | 315 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | schizoaffective disorder | targetBased | 357537 | 806 | 0.665187702963058 | 315 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | schizoaffective disorder | targetBased | 339887 | 1178 | 0.665187702963058 | 315 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | schizoaffective disorder | targetBased | 362274 | 1056 | 0.665187702963058 | 315 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | schizoaffective disorder | targetBased | 336308 | 6862 | 0.665187702963058 | 315 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | schizoaffective disorder | targetBased | 364051 | 9106 | 0.659694094276201 | 74 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | schizoaffective disorder | targetBased | 407539 | 2380 | 0.659694094276201 | 74 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | schizoaffective disorder | targetBased | 407539 | 2380 | 0.659694094276201 | 74 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | neonatal abstinence syndrome | targetBased | 335239 | 991 | 0.639503808879902 | 57 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | neonatal abstinence syndrome | targetBased | 335239 | 695 | 0.639503808879902 | 57 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | substance withdrawal syndrome | targetBased | 290355 | 265 | 0.542268057325337 | 18 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | substance withdrawal syndrome | targetBased | 335239 | 991 | 0.577358284792966 | 38 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | substance withdrawal syndrome | targetBased | 335239 | 695 | 0.577358284792966 | 38 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | hypersomnia | targetBased | 108286 | 1415 | 0.557795651831803 | 7 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | schizoaffective disorder | targetBased | 64908 | 366 | 0.647495263851435 | 45 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | schizoaffective disorder | targetBased | 61606 | 416 | 0.647495263851435 | 45 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | binge eating | targetBased | 108286 | 1415 | 0.511646077243436 | 8 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | anxiety disorder | targetBased | 363803 | 2412 | 0.565599835045342 | 93 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | anxiety disorder | targetBased | 359518 | 300 | 0.624856199454065 | 112 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | anxiety disorder | targetBased | 335652 | 1779 | 0.624856199454065 | 112 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | anxiety disorder | targetBased | 357537 | 806 | 0.624856199454065 | 112 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | anxiety disorder | targetBased | 339887 | 1178 | 0.624856199454065 | 112 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | anxiety disorder | targetBased | 362274 | 1056 | 0.624856199454065 | 112 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | anxiety disorder | targetBased | 336308 | 6862 | 0.624856199454065 | 112 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | anxiety disorder | targetBased | 364051 | 9106 | 0.548807219432151 | 18 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | anxiety disorder | targetBased | 407539 | 2380 | 0.548807219432151 | 18 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | anxiety disorder | targetBased | 407539 | 2380 | 0.548807219432151 | 18 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | anxiety disorder | targetBased | 64908 | 366 | 0.677507356279003 | 380 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | anxiety disorder | targetBased | 61606 | 416 | 0.677507356279003 | 380 |
Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | TSHR | drug use measurement | targetBased | 329153 | 670 | 0.656828814690532 | 9 |
Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | TSHR | drug use measurement | targetBased | 329153 | 670 | 0.656828814690532 | 9 |
qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor | TSHR | drug use measurement | targetBased | 72026 | 352 | 0.656828814690532 | 9 |
qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 | TSHR | drug use measurement | targetBased | 72026 | 1794 | 0.656828814690532 | 9 |
Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP_inhibitors | cerebral amyloid angiopathy | pathwayBased | 193714 | 1590 | 0.554715604164536 | 431 |
Primary screen for compounds that activate Alzheimer's amyloid precursor | APP_inhibitors | cerebral amyloid angiopathy | pathwayBased | 193400 | 1987 | 0.554715604164536 | 431 |
qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP_inhibitors | cerebral amyloid angiopathy | targetBased | 404343 | 257 | 0.554715604164536 | 431 |
TRFRET-based cell-based primary high throughput screening assay to identify inhibitors of cell surface Prion Protein (PRPC) | PRNP | cerebral amyloid angiopathy | targetBased | 369953 | 1596 | 0.739822242551998 | 67 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | postpartum depression | targetBased | 86095 | 1442 | 0.528912685748001 | 21 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | postpartum depression | targetBased | 86095 | 1151 | 0.528912685748001 | 21 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | postpartum depression | targetBased | 339772 | 8480 | 0.603347240354886 | 12 |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | Sleep Disorder | targetBased | 326024 | 5748 | 0.587025604857753 | 69 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | Sleep Disorder | targetBased | 326024 | 1387 | 0.587025604857753 | 69 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | Sleep Disorder | targetBased | 108286 | 1415 | 0.670129565809086 | 83 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | delirium | targetBased | 363803 | 2412 | 0.645294220123001 | 50 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | delirium | targetBased | 335239 | 991 | 0.62243839148902 | 20 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | delirium | targetBased | 335239 | 695 | 0.62243839148902 | 20 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | delirium | targetBased | 359518 | 300 | 0.643827981382046 | 48 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | delirium | targetBased | 335652 | 1779 | 0.643827981382046 | 48 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | delirium | targetBased | 357537 | 806 | 0.643827981382046 | 48 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | delirium | targetBased | 339887 | 1178 | 0.643827981382046 | 48 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | delirium | targetBased | 362274 | 1056 | 0.643827981382046 | 48 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | delirium | targetBased | 336308 | 6862 | 0.643827981382046 | 48 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | delirium | targetBased | 364051 | 9106 | 0.636915792851204 | 35 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | delirium | targetBased | 407539 | 2380 | 0.636915792851204 | 35 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | delirium | targetBased | 407539 | 2380 | 0.636915792851204 | 35 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | delirium | targetBased | 305610 | 3794 | 0.614214142126277 | 12 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | delirium | targetBased | 339674 | 2841 | 0.614214142126277 | 12 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | delirium | targetBased | 339772 | 8480 | 0.602430510467206 | 12 |
Dyrk1 A HTS Measured in Biochemical System Using Plate Reader - 2124-01_Inhibitor_SinglePoint_HTS_Activity | DYRK1A_inhibitors | absent or delayed speech development | targetBased | 310014 | 1321 | 0.559554695563483 | 14 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | dysthymic disorder | targetBased | 108286 | 1415 | 0.594005318047291 | 9 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | bipolar I disorder | targetBased | 363803 | 2412 | 0.662096838691452 | 110 |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | bipolar I disorder | targetBased | 315412 | 318 | 0.636160747136378 | 23 |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | bipolar I disorder | targetBased | 205582 | 727 | 0.636160747136378 | 23 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | bipolar I disorder | targetBased | 359518 | 300 | 0.663161506636499 | 119 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | bipolar I disorder | targetBased | 335652 | 1779 | 0.663161506636499 | 119 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | bipolar I disorder | targetBased | 357537 | 806 | 0.663161506636499 | 119 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | bipolar I disorder | targetBased | 339887 | 1178 | 0.663161506636499 | 119 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | bipolar I disorder | targetBased | 362274 | 1056 | 0.663161506636499 | 119 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | bipolar I disorder | targetBased | 336308 | 6862 | 0.663161506636499 | 119 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | bipolar I disorder | targetBased | 364051 | 9106 | 0.640639481752904 | 29 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | bipolar I disorder | targetBased | 407539 | 2380 | 0.640639481752904 | 29 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | bipolar I disorder | targetBased | 407539 | 2380 | 0.640639481752904 | 29 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | bipolar I disorder | targetBased | 64908 | 366 | 0.633262908369513 | 30 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | bipolar I disorder | targetBased | 61606 | 416 | 0.633262908369513 | 30 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | bipolar I disorder | targetBased | 339772 | 8480 | 0.526319275317686 | 9 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | bipolar II disorder | targetBased | 363803 | 2412 | 0.579805448943178 | 8 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | bipolar II disorder | targetBased | 359518 | 300 | 0.579839258155331 | 11 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | bipolar II disorder | targetBased | 335652 | 1779 | 0.579839258155331 | 11 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | bipolar II disorder | targetBased | 357537 | 806 | 0.579839258155331 | 11 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | bipolar II disorder | targetBased | 339887 | 1178 | 0.579839258155331 | 11 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | bipolar II disorder | targetBased | 362274 | 1056 | 0.579839258155331 | 11 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | bipolar II disorder | targetBased | 336308 | 6862 | 0.579839258155331 | 11 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | opioid use disorder | targetBased | 290355 | 265 | 0.659567124251188 | 153 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | opioid use disorder | targetBased | 335239 | 991 | 0.746624149297985 | 278 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | opioid use disorder | targetBased | 335239 | 695 | 0.746624149297985 | 278 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | treatment resistant depression | targetBased | 363803 | 2412 | 0.605959064966353 | 29 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | treatment resistant depression | targetBased | 359518 | 300 | 0.600532105955236 | 12 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | treatment resistant depression | targetBased | 335652 | 1779 | 0.600532105955236 | 12 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | treatment resistant depression | targetBased | 357537 | 806 | 0.600532105955236 | 12 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | treatment resistant depression | targetBased | 339887 | 1178 | 0.600532105955236 | 12 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | treatment resistant depression | targetBased | 362274 | 1056 | 0.600532105955236 | 12 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | treatment resistant depression | targetBased | 336308 | 6862 | 0.600532105955236 | 12 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | treatment resistant depression | targetBased | 339772 | 8480 | 0.624163682944734 | 29 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | overdose | targetBased | 335239 | 991 | 0.578681292639103 | 12 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | overdose | targetBased | 335239 | 695 | 0.578681292639103 | 12 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | pain agnosia | targetBased | 335239 | 991 | 0.60508047996565 | 11 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | pain agnosia | targetBased | 335239 | 695 | 0.60508047996565 | 11 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | generalized anxiety disorder | targetBased | 64908 | 366 | 0.595808212813299 | 59 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | generalized anxiety disorder | targetBased | 61606 | 416 | 0.595808212813299 | 59 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | social anxiety disorder | targetBased | 363803 | 2412 | 0.592744921862423 | 17 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | social anxiety disorder | targetBased | 359518 | 300 | 0.609866499579936 | 29 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | social anxiety disorder | targetBased | 335652 | 1779 | 0.609866499579936 | 29 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | social anxiety disorder | targetBased | 357537 | 806 | 0.609866499579936 | 29 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | social anxiety disorder | targetBased | 339887 | 1178 | 0.609866499579936 | 29 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | social anxiety disorder | targetBased | 362274 | 1056 | 0.609866499579936 | 29 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | social anxiety disorder | targetBased | 336308 | 6862 | 0.609866499579936 | 29 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | Agitation | targetBased | 363803 | 2412 | 0.660174078598244 | 98 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | Agitation | targetBased | 335239 | 991 | 0.619285523949174 | 12 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | Agitation | targetBased | 335239 | 695 | 0.619285523949174 | 12 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | Agitation | targetBased | 359518 | 300 | 0.660145911506038 | 99 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | Agitation | targetBased | 335652 | 1779 | 0.660145911506038 | 99 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | Agitation | targetBased | 357537 | 806 | 0.660145911506038 | 99 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | Agitation | targetBased | 339887 | 1178 | 0.660145911506038 | 99 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | Agitation | targetBased | 362274 | 1056 | 0.660145911506038 | 99 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | Agitation | targetBased | 336308 | 6862 | 0.660145911506038 | 99 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | Agitation | targetBased | 364051 | 9106 | 0.655849552139749 | 60 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | Agitation | targetBased | 407539 | 2380 | 0.655849552139749 | 60 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | Agitation | targetBased | 407539 | 2380 | 0.655849552139749 | 60 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | Agitation | targetBased | 305610 | 3794 | 0.60466648961276 | 9 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | Agitation | targetBased | 339674 | 2841 | 0.60466648961276 | 9 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | Agitation | targetBased | 64908 | 366 | 0.630698487380588 | 17 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | Agitation | targetBased | 61606 | 416 | 0.630698487380588 | 17 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | Agitation | targetBased | 339772 | 8480 | 0.560128487470336 | 8 |
Primary screen for KDM5B Histone Demethylases FDH-coupled qHTS | KDM5B | Autism | targetBased | 217819 | 5697 | 0.609806441526676 | 12 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | Dementia | targetBased | 363803 | 2412 | 0.630487519911276 | 45 |
Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP_inhibitors | Dementia | pathwayBased | 193714 | 1590 | 0.5081212394352 | 31 |
Primary screen for compounds that activate Alzheimer's amyloid precursor | APP_inhibitors | Dementia | pathwayBased | 193400 | 1987 | 0.5081212394352 | 31 |
qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP_inhibitors | Dementia | targetBased | 404343 | 257 | 0.5081212394352 | 31 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | Dementia | targetBased | 108286 | 1415 | 0.55756748337005 | 12 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | Dementia | targetBased | 359518 | 300 | 0.632086682659489 | 54 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | Dementia | targetBased | 335652 | 1779 | 0.632086682659489 | 54 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | Dementia | targetBased | 357537 | 806 | 0.632086682659489 | 54 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | Dementia | targetBased | 339887 | 1178 | 0.632086682659489 | 54 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | Dementia | targetBased | 362274 | 1056 | 0.632086682659489 | 54 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | Dementia | targetBased | 336308 | 6862 | 0.632086682659489 | 54 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | Dementia | targetBased | 364051 | 9106 | 0.591865722627954 | 15 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | Dementia | targetBased | 407539 | 2380 | 0.591865722627954 | 15 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | Dementia | targetBased | 407539 | 2380 | 0.591865722627954 | 15 |
TRFRET-based cell-based primary high throughput screening assay to identify inhibitors of cell surface Prion Protein (PRPC) | PRNP | Dementia | targetBased | 369953 | 1596 | 0.510298457303692 | 16 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | Dementia | targetBased | 339772 | 8480 | 0.645650315796052 | 30 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | Hallucinations | targetBased | 363803 | 2412 | 0.51738963111677 | 18 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | Atypical behavior | pathwayBased | 70898 | 707 | 0.666103237753127 | 22 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | Atypical behavior | pathwayBased | 131324 | 544 | 0.666103237753127 | 22 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | Specific learning disability | pathwayBased | 70898 | 707 | 0.563878136093242 | 11 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | Specific learning disability | pathwayBased | 131324 | 544 | 0.563878136093242 | 11 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | Anorexia | targetBased | 359518 | 300 | 0.539970044931212 | 18 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | Anorexia | targetBased | 335652 | 1779 | 0.539970044931212 | 18 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | Anorexia | targetBased | 357537 | 806 | 0.539970044931212 | 18 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | Anorexia | targetBased | 339887 | 1178 | 0.539970044931212 | 18 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | Anorexia | targetBased | 362274 | 1056 | 0.539970044931212 | 18 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | Anorexia | targetBased | 336308 | 6862 | 0.539970044931212 | 18 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | Borderline personality disorder | targetBased | 363803 | 2412 | 0.556262633365197 | 27 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | Borderline personality disorder | targetBased | 359518 | 300 | 0.559271258805975 | 23 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | Borderline personality disorder | targetBased | 335652 | 1779 | 0.559271258805975 | 23 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | Borderline personality disorder | targetBased | 357537 | 806 | 0.559271258805975 | 23 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | Borderline personality disorder | targetBased | 339887 | 1178 | 0.559271258805975 | 23 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | Borderline personality disorder | targetBased | 362274 | 1056 | 0.559271258805975 | 23 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | Borderline personality disorder | targetBased | 336308 | 6862 | 0.559271258805975 | 23 |
Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP_inhibitors | dementia | pathwayBased | 193714 | 1590 | 0.583153557937084 | 700 |
Primary screen for compounds that activate Alzheimer's amyloid precursor | APP_inhibitors | dementia | pathwayBased | 193400 | 1987 | 0.583153557937084 | 700 |
qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP_inhibitors | dementia | targetBased | 404343 | 257 | 0.583153557937084 | 700 |
TRFRET-based cell-based primary high throughput screening assay to identify inhibitors of cell surface Prion Protein (PRPC) | PRNP | dementia | targetBased | 369953 | 1596 | 0.521539092706237 | 119 |
qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | MAPT | dementia | pathwayBased | 267412 | 5703 | 0.55546276458891 | 1658 |
qHTS Assay for Tau Filament Binding | MAPT | dementia | targetBased | 69668 | 1391 | 0.55546276458891 | 1658 |
qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | MAPT | dementia | pathwayBased | 271402 | 1048 | 0.55546276458891 | 1658 |
Development of Small Molecule Probes of the Histone Methyltransferase, NSD2 Measured in Biochemical System Using Plate Reader - 7053-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | NSD2 | syndromic intellectual disability | targetBased | 309684 | 1662 | 0.546843946436569 | 7 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | major depressive disorder | targetBased | 290355 | 265 | 0.596086455816202 | 42 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | major depressive disorder | targetBased | 363803 | 2412 | 0.693202281364196 | 303 |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | major depressive disorder | targetBased | 315412 | 318 | 0.583510030116279 | 12 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | major depressive disorder | targetBased | 335239 | 991 | 0.592300374829612 | 44 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | major depressive disorder | targetBased | 335239 | 695 | 0.592300374829612 | 44 |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | major depressive disorder | targetBased | 205582 | 727 | 0.583510030116279 | 12 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | major depressive disorder | targetBased | 108286 | 1415 | 0.684232928654062 | 180 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | major depressive disorder | targetBased | 359518 | 300 | 0.77144510239322 | 225 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | major depressive disorder | targetBased | 335652 | 1779 | 0.77144510239322 | 225 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | major depressive disorder | targetBased | 357537 | 806 | 0.77144510239322 | 225 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | major depressive disorder | targetBased | 339887 | 1178 | 0.77144510239322 | 225 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | major depressive disorder | targetBased | 362274 | 1056 | 0.77144510239322 | 225 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | major depressive disorder | targetBased | 336308 | 6862 | 0.77144510239322 | 225 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | major depressive disorder | targetBased | 364051 | 9106 | 0.644790053219678 | 33 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | major depressive disorder | targetBased | 407539 | 2380 | 0.644790053219678 | 33 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | major depressive disorder | targetBased | 407539 | 2380 | 0.644790053219678 | 33 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | major depressive disorder | targetBased | 64908 | 366 | 0.695750938597305 | 389 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | major depressive disorder | targetBased | 61606 | 416 | 0.695750938597305 | 389 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | major depressive disorder | targetBased | 339772 | 8480 | 0.654704899119961 | 125 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | alcohol abuse | targetBased | 363803 | 2412 | 0.521574715878931 | 11 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | alcohol abuse | targetBased | 359518 | 300 | 0.52882174426934 | 68 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | alcohol abuse | targetBased | 335652 | 1779 | 0.52882174426934 | 68 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | alcohol abuse | targetBased | 357537 | 806 | 0.52882174426934 | 68 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | alcohol abuse | targetBased | 339887 | 1178 | 0.52882174426934 | 68 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | alcohol abuse | targetBased | 362274 | 1056 | 0.52882174426934 | 68 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | alcohol abuse | targetBased | 336308 | 6862 | 0.52882174426934 | 68 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | depressive disorder | targetBased | 290355 | 265 | 0.610437333238209 | 44 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | depressive disorder | targetBased | 86095 | 1442 | 0.568729888416492 | 32 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | depressive disorder | targetBased | 86095 | 1151 | 0.568729888416492 | 32 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | depressive disorder | targetBased | 363803 | 2412 | 0.671961291843088 | 359 |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | depressive disorder | targetBased | 315412 | 318 | 0.641528774775255 | 33 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | depressive disorder | targetBased | 335239 | 991 | 0.619661194229996 | 48 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | depressive disorder | targetBased | 335239 | 695 | 0.619661194229996 | 48 |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | depressive disorder | targetBased | 205582 | 727 | 0.641258301078033 | 33 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | depressive disorder | targetBased | 86095 | 1114 | 0.553635020531971 | 10 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | depressive disorder | targetBased | 108286 | 1415 | 0.667053686218244 | 313 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | depressive disorder | targetBased | 359518 | 300 | 0.702767776105905 | 257 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | depressive disorder | targetBased | 335652 | 1779 | 0.702767776105905 | 257 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | depressive disorder | targetBased | 357537 | 806 | 0.702767776105905 | 257 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | depressive disorder | targetBased | 339887 | 1178 | 0.702767776105905 | 257 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | depressive disorder | targetBased | 362274 | 1056 | 0.702767776105905 | 257 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | depressive disorder | targetBased | 336308 | 6862 | 0.702767776105905 | 257 |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | depressive disorder | targetBased | 276265 | 806 | 0.598348996827665 | 10 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | depressive disorder | targetBased | 364051 | 9106 | 0.660408365269154 | 68 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | depressive disorder | targetBased | 407539 | 2380 | 0.660408365269154 | 68 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | depressive disorder | targetBased | 407539 | 2380 | 0.660408365269154 | 68 |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | depressive disorder | targetBased | 335239 | 2035 | 0.505733262637839 | 22 |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | depressive disorder | targetBased | 335239 | 279 | 0.505733262637839 | 22 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | depressive disorder | targetBased | 64908 | 366 | 0.663494633120395 | 264 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | depressive disorder | targetBased | 61606 | 416 | 0.663494633120395 | 264 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | depressive disorder | targetBased | 339772 | 8480 | 0.659245989128873 | 186 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | tic disorder | targetBased | 363803 | 2412 | 0.558316127425329 | 18 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | tic disorder | targetBased | 359518 | 300 | 0.580042296367147 | 42 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | tic disorder | targetBased | 335652 | 1779 | 0.580042296367147 | 42 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | tic disorder | targetBased | 357537 | 806 | 0.580042296367147 | 42 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | tic disorder | targetBased | 339887 | 1178 | 0.580042296367147 | 42 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | tic disorder | targetBased | 362274 | 1056 | 0.580042296367147 | 42 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | tic disorder | targetBased | 336308 | 6862 | 0.580042296367147 | 42 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | tic disorder | targetBased | 64908 | 366 | 0.546400426458304 | 13 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | tic disorder | targetBased | 61606 | 416 | 0.546400426458304 | 13 |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | depressive disorder | targetBased | 359207 | 1189 | 0.518981413439618 | 11 |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | depressive disorder | targetBased | 63676 | 1938 | 0.518981413439618 | 11 |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | depressive disorder | targetBased | 359207 | 316 | 0.518981413439618 | 11 |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | depressive disorder | targetBased | 63656 | 2179 | 0.518981413439618 | 11 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | depressive disorder | targetBased | 359207 | 4555 | 0.518981413439618 | 11 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | substance abuse | targetBased | 363803 | 2412 | 0.57215424526313 | 13 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | substance abuse | targetBased | 108286 | 1415 | 0.526861384355099 | 57 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | substance abuse | targetBased | 359518 | 300 | 0.577999965458365 | 102 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | substance abuse | targetBased | 335652 | 1779 | 0.577999965458365 | 102 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | substance abuse | targetBased | 357537 | 806 | 0.577999965458365 | 102 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | substance abuse | targetBased | 339887 | 1178 | 0.577999965458365 | 102 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | substance abuse | targetBased | 362274 | 1056 | 0.577999965458365 | 102 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | substance abuse | targetBased | 336308 | 6862 | 0.577999965458365 | 102 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | substance dependence | targetBased | 363803 | 2412 | 0.562245621886424 | 59 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | substance dependence | targetBased | 108286 | 1415 | 0.606253414937565 | 201 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | substance dependence | targetBased | 359518 | 300 | 0.593933381960675 | 250 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | substance dependence | targetBased | 335652 | 1779 | 0.593933381960675 | 250 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | substance dependence | targetBased | 357537 | 806 | 0.593933381960675 | 250 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | substance dependence | targetBased | 339887 | 1178 | 0.593933381960675 | 250 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | substance dependence | targetBased | 362274 | 1056 | 0.593933381960675 | 250 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | substance dependence | targetBased | 336308 | 6862 | 0.593933381960675 | 250 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | schizophrenia | targetBased | 290355 | 265 | 0.528898327260153 | 32 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | schizophrenia | targetBased | 363803 | 2412 | 0.684251885809616 | 2878 |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | schizophrenia | targetBased | 315412 | 318 | 0.510856626964792 | 17 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | schizophrenia | targetBased | 335239 | 991 | 0.537788597367771 | 37 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | schizophrenia | targetBased | 335239 | 695 | 0.537788597367771 | 37 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | schizophrenia | targetBased | 86095 | 1114 | 0.743395452086089 | 48 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | schizophrenia | targetBased | 108286 | 1415 | 0.681178593375036 | 351 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | schizophrenia | targetBased | 359518 | 300 | 0.803689936994135 | 4030 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | schizophrenia | targetBased | 335652 | 1779 | 0.803689936994135 | 4030 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | schizophrenia | targetBased | 357537 | 806 | 0.803689936994135 | 4030 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | schizophrenia | targetBased | 339887 | 1178 | 0.803689936994135 | 4030 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | schizophrenia | targetBased | 362274 | 1056 | 0.803689936994135 | 4030 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | schizophrenia | targetBased | 336308 | 6862 | 0.803689936994135 | 4030 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | schizophrenia | targetBased | 364051 | 9106 | 0.773518981697282 | 911 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | schizophrenia | targetBased | 407539 | 2380 | 0.773518981697282 | 911 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | schizophrenia | targetBased | 407539 | 2380 | 0.773518981697282 | 911 |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | schizophrenia | targetBased | 335239 | 2035 | 0.65253676906973 | 96 |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | schizophrenia | targetBased | 335239 | 279 | 0.65253676906973 | 96 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | bipolar disorder | targetBased | 363803 | 2412 | 0.673380276889437 | 1227 |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | schizophrenia | targetBased | 359207 | 1189 | 0.58146298491719 | 81 |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | schizophrenia | targetBased | 63676 | 1938 | 0.58146298491719 | 81 |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | schizophrenia | targetBased | 359207 | 316 | 0.58146298491719 | 81 |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | schizophrenia | targetBased | 63656 | 2179 | 0.58146298491719 | 81 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | schizophrenia | targetBased | 359207 | 4555 | 0.58146298491719 | 81 |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | schizophrenia | targetBased | 64908 | 446 | 0.646240142990496 | 35 |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | schizophrenia | targetBased | 64908 | 641 | 0.646240142990496 | 35 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | schizophrenia | targetBased | 64908 | 366 | 0.683528594348945 | 696 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | schizophrenia | targetBased | 61606 | 416 | 0.683528594348945 | 696 |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | schizophrenia | targetBased | 324747 | 1043 | 0.576028462802304 | 99 |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | schizophrenia | targetBased | 361330 | 3713 | 0.556751417718264 | 233 |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | schizophrenia | targetBased | 57705 | 3413 | 0.556751417718264 | 233 |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | schizophrenia | targetBased | 355805 | 11440 | 0.556751417718264 | 233 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | schizophrenia | targetBased | 339772 | 8480 | 0.629740114179662 | 65 |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | bipolar disorder | targetBased | 315412 | 318 | 0.664011412408151 | 167 |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | bipolar disorder | targetBased | 205582 | 727 | 0.666223962413413 | 179 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | bipolar disorder | targetBased | 108286 | 1415 | 0.62804776439785 | 139 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | bipolar disorder | targetBased | 359518 | 300 | 0.784698432000525 | 1317 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | bipolar disorder | targetBased | 335652 | 1779 | 0.784698432000525 | 1317 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | bipolar disorder | targetBased | 357537 | 806 | 0.784698432000525 | 1317 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | bipolar disorder | targetBased | 339887 | 1178 | 0.784698432000525 | 1317 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | bipolar disorder | targetBased | 362274 | 1056 | 0.784698432000525 | 1317 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | bipolar disorder | targetBased | 336308 | 6862 | 0.784698432000525 | 1317 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | bipolar disorder | targetBased | 364051 | 9106 | 0.669375228835304 | 280 |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | bipolar disorder | targetBased | 407539 | 2380 | 0.669375228835304 | 280 |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | bipolar disorder | targetBased | 407539 | 2380 | 0.669375228835304 | 280 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | bipolar disorder | targetBased | 64908 | 366 | 0.664540949556231 | 143 |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | bipolar disorder | targetBased | 61606 | 416 | 0.664540949556231 | 143 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | bipolar disorder | targetBased | 339772 | 8480 | 0.636690276883609 | 44 |
Luminescence cell-based high throughput primary assay to identify inhibitors of TEAD-YAP interaction. | YAP1 | uveal coloboma-cleft lip and palate-intellectual disability | targetBased | 639428 | 9218 | 0.738514274092363 | 21 |
TRFRET-based cell-based primary high throughput screening assay to identify inhibitors of cell surface Prion Protein (PRPC) | PRNP | inherited Creutzfeldt-Jakob disease | targetBased | 369953 | 1596 | 0.837038041259018 | 132 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | alcohol dependence | targetBased | 290355 | 265 | 0.670607044489001 | 198 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | alcohol dependence | targetBased | 363803 | 2412 | 0.586130803291848 | 66 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | alcohol dependence | targetBased | 335239 | 991 | 0.673240401913081 | 285 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | alcohol dependence | targetBased | 335239 | 695 | 0.673240401913081 | 285 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | alcohol dependence | targetBased | 359518 | 300 | 0.664778854425383 | 200 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | alcohol dependence | targetBased | 335652 | 1779 | 0.664778854425383 | 200 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | alcohol dependence | targetBased | 357537 | 806 | 0.664778854425383 | 200 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | alcohol dependence | targetBased | 339887 | 1178 | 0.664778854425383 | 200 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | alcohol dependence | targetBased | 362274 | 1056 | 0.664778854425383 | 200 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | alcohol dependence | targetBased | 336308 | 6862 | 0.664778854425383 | 200 |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | alcohol dependence | targetBased | 324747 | 1043 | 0.539074368589372 | 32 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | alcohol dependence | targetBased | 339772 | 8480 | 0.648735442562118 | 57 |
TRFRET-based cell-based primary high throughput screening assay to identify inhibitors of cell surface Prion Protein (PRPC) | PRNP | Gerstmann-Straussler-Scheinker syndrome | targetBased | 369953 | 1596 | 0.893488295726227 | 213 |
Development of Small Molecule Probes of the Histone Methyltransferase, NSD2 Measured in Biochemical System Using Plate Reader - 7053-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | NSD2 | Wolf-Hirschhorn syndrome | targetBased | 309684 | 1662 | 0.580036883778645 | 149 |
Glucocerebrosidase | GBA1 | Gaucher disease type I | targetBased | 48118 | 549 | 0.878031247240919 | 443 |
Glucocerebrosidase | GBA1 | Gaucher disease type II | targetBased | 48118 | 549 | 0.855638338257464 | 192 |
Primary qHTS for Inhibitors of ATXN expression | ATXN2_repressors | spinocerebellar ataxia type 2 | targetBased | 358434 | 2554 | 0.731331827352406 | 473 |
TRFRET-based cell-based primary high throughput screening assay to identify inhibitors of cell surface Prion Protein (PRPC) | PRNP | fatal familial insomnia | targetBased | 369953 | 1596 | 0.7364832327914 | 188 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the HTRA serine peptidase 1 (HTRA1) | HTRA1 | CARASIL syndrome | targetBased | 343467 | 1710 | 0.784936074971295 | 51 |
qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | MAPT | semantic dementia | pathwayBased | 267412 | 5703 | 0.847634887281404 | 330 |
qHTS Assay for Tau Filament Binding | MAPT | semantic dementia | targetBased | 69668 | 1391 | 0.847634887281404 | 330 |
qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | MAPT | semantic dementia | pathwayBased | 271402 | 1048 | 0.847634887281404 | 330 |
Luminescence-based cell-based primary high throughput screening assay to identify activators of the function of SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 (SMARCA2, BRM) | SMARCA2 | intellectual disability-sparse hair-brachydactyly syndrome | targetBased | 368927 | 3838 | 0.903276780005793 | 93 |
TRFRET-based cell-based primary high throughput screening assay to identify inhibitors of cell surface Prion Protein (PRPC) | PRNP | Huntington disease-like 1 | targetBased | 369953 | 1596 | 0.843396184087878 | 176 |
qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen | TARDBP | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions | pathwayBased | 45163 | 203 | 0.605944606681798 | 205 |
qHTS of TDP-43 Inhibitors | TARDBP | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions | pathwayBased | 403703 | 7150 | 0.605944606681798 | 205 |
Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP_inhibitors | cerebral amyloid angiopathy, APP-related | pathwayBased | 193714 | 1590 | 0.826810281381391 | 53 |
Primary screen for compounds that activate Alzheimer's amyloid precursor | APP_inhibitors | cerebral amyloid angiopathy, APP-related | pathwayBased | 193400 | 1987 | 0.826810281381391 | 53 |
qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP_inhibitors | cerebral amyloid angiopathy, APP-related | targetBased | 404343 | 257 | 0.826810281381391 | 53 |
uHTS identification of DNMT1 inhibitors in a Fluorescent Molecular Beacon assay | DNMT1 | autosomal dominant cerebellar ataxia, deafness and narcolepsy | targetBased | 359244 | 2975 | 0.8534316413014 | 93 |
qHTS Assay for Identification of Novel General Anesthetics | FTL | neuroferritinopathy | targetBased | 341499 | 255 | 0.835274341530147 | 296 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | Birk-Barel syndrome | targetBased | 305610 | 3794 | 0.771166979421912 | 51 |
High Throughput Imaging Assay for Beta-Catenin | betaCateninTranslocation | severe intellectual disability-progressive spastic diplegia syndrome | targetBased | 193542 | 587 | 0.869266163504584 | 149 |
Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP_inhibitors | ABeta amyloidosis, dutch type | pathwayBased | 193714 | 1590 | 0.500813042182858 | 9 |
Primary screen for compounds that activate Alzheimer's amyloid precursor | APP_inhibitors | ABeta amyloidosis, dutch type | pathwayBased | 193400 | 1987 | 0.500813042182858 | 9 |
qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP_inhibitors | ABeta amyloidosis, dutch type | targetBased | 404343 | 257 | 0.500813042182858 | 9 |
Dyrk1 A HTS Measured in Biochemical System Using Plate Reader - 2124-01_Inhibitor_SinglePoint_HTS_Activity | DYRK1A_inhibitors | DYRK1A-related intellectual disability syndrome | targetBased | 310014 | 1321 | 0.808262884097842 | 1089 |
Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP_inhibitors | early-onset autosomal dominant Alzheimer disease | pathwayBased | 193714 | 1590 | 0.602429390128475 | 128 |
Primary screen for compounds that activate Alzheimer's amyloid precursor | APP_inhibitors | early-onset autosomal dominant Alzheimer disease | pathwayBased | 193400 | 1987 | 0.602429390128475 | 128 |
qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP_inhibitors | early-onset autosomal dominant Alzheimer disease | targetBased | 404343 | 257 | 0.602429390128475 | 128 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the HTRA serine peptidase 1 (HTRA1) | HTRA1 | cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 | targetBased | 343467 | 1710 | 0.83274242648193 | 85 |
Epi Absorbance-based biochemical primary high throughput screening assay to identify inhibitors of human tyrosyl-DNA phosphodiesterase 2 (TDP2) | TDP2 | spinocerebellar ataxia, autosomal recessive 23 | targetBased | 369953 | 1241 | 0.719126736741118 | 27 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | narcolepsy-cataplexy syndrome | targetBased | 108286 | 1415 | 0.649086161600151 | 35 |
Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP_inhibitors | ABeta amyloidosis, Iowa type | pathwayBased | 193714 | 1590 | 0.501814132954698 | 6 |
Primary screen for compounds that activate Alzheimer's amyloid precursor | APP_inhibitors | ABeta amyloidosis, Iowa type | pathwayBased | 193400 | 1987 | 0.501814132954698 | 6 |
qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP_inhibitors | ABeta amyloidosis, Iowa type | targetBased | 404343 | 257 | 0.501814132954698 | 6 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ2 potassium channels | KCNQ2 | West syndrome | targetBased | 305609 | 3405 | 0.542134231909906 | 11 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate KCNQ2 potassium channels | KCNQ2 | West syndrome | targetBased | 305600 | 1644 | 0.542134231909906 | 11 |
qHTS Assay for Inhibitors of the CtBP/E1A Interaction | RBBP8 | Seckel syndrome | targetBased | 335214 | 1652 | 0.563779003089398 | 24 |
Primary screen for KDM5B Histone Demethylases FDH-coupled qHTS | KDM5B | autosomal recessive non-syndromic intellectual disability | targetBased | 217819 | 5697 | 0.537940614194576 | 28 |
Primary screen for KDM5B Histone Demethylases FDH-coupled qHTS | KDM5B | intellectual disability, autosomal recessive 65 | targetBased | 217819 | 5697 | 0.777855262897303 | 78 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | alcohol-related disorders | targetBased | 290355 | 265 | 0.507369097179461 | 79 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | alcohol-related disorders | targetBased | 335239 | 991 | 0.508266406705186 | 113 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | alcohol-related disorders | targetBased | 335239 | 695 | 0.508266406705186 | 113 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | narcolepsy | targetBased | 108286 | 1415 | 0.511411229293004 | 40 |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | enuresis | targetBased | 324747 | 813 | 0.643223221917796 | 27 |
qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | MAPT | Classical progressive supranuclear palsy | pathwayBased | 267412 | 5703 | 0.724714707725161 | 50 |
qHTS Assay for Tau Filament Binding | MAPT | Classical progressive supranuclear palsy | targetBased | 69668 | 1391 | 0.724714707725161 | 50 |
qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | MAPT | Classical progressive supranuclear palsy | pathwayBased | 271402 | 1048 | 0.724714707725161 | 50 |
qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | MAPT | Progressive supranuclear palsy - parkinsonism | pathwayBased | 267412 | 5703 | 0.673064875545468 | 26 |
qHTS Assay for Tau Filament Binding | MAPT | Progressive supranuclear palsy - parkinsonism | targetBased | 69668 | 1391 | 0.673064875545468 | 26 |
qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | MAPT | Progressive supranuclear palsy - parkinsonism | pathwayBased | 271402 | 1048 | 0.673064875545468 | 26 |
qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) | HSD17B10 | HSD10 disease | targetBased | 72072 | 2464 | 0.865073065613424 | 59 |
qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 | HSD17B10 | HSD10 disease | targetBased | 73912 | 5649 | 0.865073065613424 | 59 |
qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | MAPT | Atypical progressive supranuclear palsy | pathwayBased | 267412 | 5703 | 0.689294807696597 | 33 |
qHTS Assay for Tau Filament Binding | MAPT | Atypical progressive supranuclear palsy | targetBased | 69668 | 1391 | 0.689294807696597 | 33 |
qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | MAPT | Atypical progressive supranuclear palsy | pathwayBased | 271402 | 1048 | 0.689294807696597 | 33 |
Some of these associations have also gone through clinical trials, as those in the graph below.
Find clinical trials details in table. Use scroll bar or search funtion to select specific drugs, molecular targets or diseases.
BioAssay Name | program | gene | protName | diseaseName | molname | assayMode | clinicalPhase | clinicalStatus | studyStartDate | url | score | variantEffect | directionOnTrait | studyStopReason |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | AMPHETAMINE | targetBased | 4 | Completed | 01/12/2010 | https://clinicaltrials.gov/study/NCT02058693 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | AMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | AMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bb12811f-4cce-4010-aa48-d17c46ca1d3a | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | AMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f469fb38-0380-4621-9db3-a4f429126156 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | AMPHETAMINE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT02020408 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c1179269-00b5-48ea-972d-31e614e99b7e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE | targetBased | 4 | Recruiting | 01/07/2018 | https://clinicaltrials.gov/study/NCT03153488 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06BA01 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f469fb38-0380-4621-9db3-a4f429126156 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=eb1cc8d0-4231-41ea-8535-4fd872129713 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE | targetBased | 4 | Completed | 07/05/2018 | https://clinicaltrials.gov/study/NCT03610464 | 1 | protect | ||
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | bipolar disorder | VERAPAMIL | targetBased | 3 | Completed | 01/11/1994 | https://clinicaltrials.gov/study/NCT00518947 | 0.7 | LoF | protect | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | circadian rhythm sleep disorder | DILTIAZEM | targetBased | 4 | Completed | 01/06/2009 | https://clinicaltrials.gov/study/NCT01914926 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUOPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB06 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | SULPIRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | SULPIRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | SULPIRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL01 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | SULPIRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | SULPIRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | SULPIRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | SULPIRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | SULPIRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | social anxiety disorder | PROPRANOLOL | targetBased | 4 | Terminated | 01/06/2016 | https://clinicaltrials.gov/study/NCT02790736 | 1 | LoF | protect | COVID-19 restrictions |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | social anxiety disorder | PROPRANOLOL | targetBased | 4 | Not yet recruiting | 01/10/2016 | https://clinicaltrials.gov/study/NCT02924610 | 1 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | anxiety | PROPRANOLOL | targetBased | 4 | Completed | 16/06/2014 | https://clinicaltrials.gov/study/NCT02153944 | 1 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | post-traumatic stress disorder | PROPRANOLOL | targetBased | 4 | Terminated | 01/04/2008 | https://clinicaltrials.gov/study/NCT00645450 | 1 | LoF | protect | Difficulty recruiting subjects and loss of study physician for new job |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | post-traumatic stress disorder | PROPRANOLOL | targetBased | 4 | Terminated | 01/12/2003 | https://clinicaltrials.gov/study/NCT00648375 | 1 | LoF | protect | inadequate recruitment |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | post-traumatic stress disorder | PROPRANOLOL | targetBased | 4 | Completed | 01/05/2007 | https://clinicaltrials.gov/study/NCT00709735 | 1 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | post-traumatic stress disorder | PROPRANOLOL | targetBased | 4 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00158262 | 1 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | post-traumatic stress disorder | PROPRANOLOL | targetBased | 3 | Recruiting | 01/02/2023 | https://clinicaltrials.gov/study/NCT04985344 | 0.7 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | post-traumatic stress disorder | PROPRANOLOL | targetBased | 3 | Completed | 27/05/2016 | https://clinicaltrials.gov/study/NCT02789982 | 0.7 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | post-traumatic stress disorder | PROPRANOLOL | targetBased | 3 | Terminated | 01/09/2010 | https://clinicaltrials.gov/study/NCT01239173 | 0.7 | LoF | protect | Study stopped by promoter for lack of inclusion |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | post-traumatic stress disorder | PROPRANOLOL | targetBased | 4 | Recruiting | 15/06/2023 | https://clinicaltrials.gov/study/NCT05853627 | 1 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | obsessive-compulsive disorder | PROPRANOLOL | targetBased | 4 | Withdrawn | 01/06/2016 | https://clinicaltrials.gov/study/NCT02790710 | 1 | LoF | protect | Study has been withdrawn due to reconsideration of study design. |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | nicotine dependence | PROPRANOLOL | targetBased | 4 | Not yet recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT05587361 | 1 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | nicotine dependence | PROPRANOLOL | targetBased | 4 | Completed | 16/01/2018 | https://clinicaltrials.gov/study/NCT03309943 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CLOZAPINE | targetBased | 4 | Recruiting | 01/08/2016 | https://clinicaltrials.gov/study/NCT02639702 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/08/1998 | https://clinicaltrials.gov/study/NCT00169065 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CLOZAPINE | targetBased | 4 | Terminated | 01/12/1994 | https://clinicaltrials.gov/study/NCT00169039 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00501618 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01663077 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CLOZAPINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/09/2015 | https://clinicaltrials.gov/study/NCT02625103 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CLOZAPINE | targetBased | 4 | Unknown status | 01/10/2015 | https://clinicaltrials.gov/study/NCT02562287 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CLOZAPINE | targetBased | 4 | Unknown status | 01/10/2015 | https://clinicaltrials.gov/study/NCT02562287 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | CLOZAPINE | targetBased | 4 | Unknown status | 01/10/2015 | https://clinicaltrials.gov/study/NCT02562287 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | CLOZAPINE | targetBased | 4 | Unknown status | 01/10/2015 | https://clinicaltrials.gov/study/NCT02562287 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CLOZAPINE | targetBased | 4 | Unknown status | 01/10/2015 | https://clinicaltrials.gov/study/NCT02562287 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CLOZAPINE | targetBased | 4 | Unknown status | 01/10/2015 | https://clinicaltrials.gov/study/NCT02562287 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CLOZAPINE | targetBased | 3 | Completed | 01/05/2002 | https://clinicaltrials.gov/study/NCT00036582 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | CLOZAPINE | targetBased | 4 | Completed | 01/06/1997 | https://clinicaltrials.gov/study/NCT00001656 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | CLOZAPINE | targetBased | 4 | Withdrawn | 01/01/2015 | https://clinicaltrials.gov/study/NCT02286206 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment refractory schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/02/2019 | https://clinicaltrials.gov/study/NCT03807882 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | panic disorder | CLOZAPINE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00031317 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=693cb9d4-39db-4ecf-9eae-b01f06f8d5d1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b7b7541a-1fe4-4b11-b6b7-68fb5510faa4 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b7b7541a-1fe4-4b11-b6b7-68fb5510faa4 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b7b7541a-1fe4-4b11-b6b7-68fb5510faa4 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b7b7541a-1fe4-4b11-b6b7-68fb5510faa4 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b7b7541a-1fe4-4b11-b6b7-68fb5510faa4 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b7b7541a-1fe4-4b11-b6b7-68fb5510faa4 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | panic disorder | CLOZAPINE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00031317 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | panic disorder | CLOZAPINE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00031317 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | panic disorder | CLOZAPINE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00031317 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | panic disorder | CLOZAPINE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00031317 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | panic disorder | CLOZAPINE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00031317 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | panic disorder | CLOZAPINE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00031317 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | CLOZAPINE | targetBased | 4 | Unknown status | 01/10/2015 | https://clinicaltrials.gov/study/NCT02562287 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | CLOZAPINE | targetBased | 3 | Completed | 01/05/2002 | https://clinicaltrials.gov/study/NCT00036582 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CLOZAPINE | targetBased | 4 | Completed | 01/06/1997 | https://clinicaltrials.gov/study/NCT00001656 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CLOZAPINE | targetBased | 4 | Withdrawn | 01/01/2015 | https://clinicaltrials.gov/study/NCT02286206 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CLOZAPINE | targetBased | 4 | Withdrawn | 01/01/2015 | https://clinicaltrials.gov/study/NCT02286206 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CLOZAPINE | targetBased | 4 | Withdrawn | 01/01/2015 | https://clinicaltrials.gov/study/NCT02286206 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CLOZAPINE | targetBased | 4 | Withdrawn | 01/01/2015 | https://clinicaltrials.gov/study/NCT02286206 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CLOZAPINE | targetBased | 4 | Withdrawn | 01/01/2015 | https://clinicaltrials.gov/study/NCT02286206 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CLOZAPINE | targetBased | 4 | Withdrawn | 01/01/2015 | https://clinicaltrials.gov/study/NCT02286206 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/02/2019 | https://clinicaltrials.gov/study/NCT03807882 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/02/2019 | https://clinicaltrials.gov/study/NCT03807882 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/02/2019 | https://clinicaltrials.gov/study/NCT03807882 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/02/2019 | https://clinicaltrials.gov/study/NCT03807882 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/02/2019 | https://clinicaltrials.gov/study/NCT03807882 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | CLOZAPINE | targetBased | 4 | Completed | 01/02/2019 | https://clinicaltrials.gov/study/NCT03807882 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | CLOZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH02 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | CLOZAPINE | targetBased | 4 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00501618 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | CLOZAPINE | targetBased | 4 | Completed | 01/03/2009 | https://clinicaltrials.gov/study/NCT00981526 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=47c4897c-ee95-4eaf-adbc-84130d021d2d | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | CLOZAPINE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | CLOZAPINE | targetBased | 4 | Completed | 01/05/1999 | https://clinicaltrials.gov/study/NCT02640300 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=883b5d43-0339-7dc1-f775-93791fb9b978 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=90876802-0e3a-44c9-9ff7-1754dfbe736a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | CLOZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | CLOZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | CLOZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH02 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | CLOZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | CLOZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | CLOZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH02 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | CLOZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CLOZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=883b5d43-0339-7dc1-f775-93791fb9b978 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CLOZAPINE | targetBased | 4 | Recruiting | 28/02/2021 | https://clinicaltrials.gov/study/NCT05316883 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CLOZAPINE | targetBased | 4 | Recruiting | 28/02/2021 | https://clinicaltrials.gov/study/NCT05316883 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CLOZAPINE | targetBased | 4 | Recruiting | 28/02/2021 | https://clinicaltrials.gov/study/NCT05316883 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CLOZAPINE | targetBased | 4 | Recruiting | 28/02/2021 | https://clinicaltrials.gov/study/NCT05316883 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CLOZAPINE | targetBased | 4 | Recruiting | 28/02/2021 | https://clinicaltrials.gov/study/NCT05316883 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CLOZAPINE | targetBased | 4 | Recruiting | 28/02/2021 | https://clinicaltrials.gov/study/NCT05316883 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | cannabis dependence | BUSPIRONE | targetBased | 4 | Completed | 01/09/2009 | https://clinicaltrials.gov/study/NCT00875836 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | cannabis dependence | BUSPIRONE | targetBased | 4 | Completed | 01/09/2009 | https://clinicaltrials.gov/study/NCT00875836 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism spectrum disorder | BUSPIRONE | targetBased | 4 | Completed | 31/10/2018 | https://clinicaltrials.gov/study/NCT03538431 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism spectrum disorder | BUSPIRONE | targetBased | 4 | Completed | 31/10/2018 | https://clinicaltrials.gov/study/NCT03538431 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BUSPIRONE | targetBased | 4 | Unknown status | 01/08/2014 | https://clinicaltrials.gov/study/NCT02273154 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BUSPIRONE | targetBased | 4 | Unknown status | 01/08/2014 | https://clinicaltrials.gov/study/NCT02273154 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BUSPIRONE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00021528 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BUSPIRONE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00021528 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BUSPIRONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19a92a99-f73a-42f5-b048-28ba0b4df9e6 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19a92a99-f73a-42f5-b048-28ba0b4df9e6 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | heroin dependence | BUSPIRONE | targetBased | 4 | Completed | 01/01/2002 | https://clinicaltrials.gov/study/NCT00326235 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | heroin dependence | BUSPIRONE | targetBased | 4 | Completed | 01/01/2002 | https://clinicaltrials.gov/study/NCT00326235 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0568f0c0-2f05-374d-11bf-c74796629535 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bbf2015c-0093-4e53-b25e-33f5d2987a7a | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bbf2015c-0093-4e53-b25e-33f5d2987a7a | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f61184d1-e34a-4a84-9432-a7bacf09e818 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f61184d1-e34a-4a84-9432-a7bacf09e818 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ed60a885-6b02-48c8-979f-27d371e91d6e | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ed60a885-6b02-48c8-979f-27d371e91d6e | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | BUSPIRONE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00178971 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | BUSPIRONE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00178971 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BUSPIRONE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00178971 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BUSPIRONE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00178971 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BUSPIRONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BUSPIRONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | BUSPIRONE | targetBased | 4 | Withdrawn | 01/03/2012 | https://clinicaltrials.gov/study/NCT01546896 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | BUSPIRONE | targetBased | 4 | Withdrawn | 01/03/2012 | https://clinicaltrials.gov/study/NCT01546896 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | BUSPIRONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05BE01 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | BUSPIRONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05BE01 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | BUSPIRONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | BUSPIRONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | BUSPIRONE | targetBased | 3 | Recruiting | 24/07/2023 | https://clinicaltrials.gov/study/NCT06243614 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | BUSPIRONE | targetBased | 3 | Recruiting | 24/07/2023 | https://clinicaltrials.gov/study/NCT06243614 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19a92a99-f73a-42f5-b048-28ba0b4df9e6 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | BUSPIRONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19a92a99-f73a-42f5-b048-28ba0b4df9e6 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Dementia | BUSPIRONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Dementia | BUSPIRONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | MOLINDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | MOLINDONE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00053703 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | MOLINDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | MOLINDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | MOLINDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | MOLINDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE02 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | MOLINDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | MOLINDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | MOLINDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE02 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Terminated | 01/04/2016 | https://clinicaltrials.gov/study/NCT02691182 | 0.35 | LoF | protect | The program was shut down due to a lack of efficacy. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 25/01/2016 | https://clinicaltrials.gov/study/NCT02618408 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 16/02/2016 | https://clinicaltrials.gov/study/NCT02618434 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Terminated | 31/07/2018 | https://clinicaltrials.gov/study/NCT03597503 | 0.7 | LoF | protect | Business decision, not related to safety |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00053703 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 16/02/2016 | https://clinicaltrials.gov/study/NCT02618434 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 16/02/2016 | https://clinicaltrials.gov/study/NCT02618434 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 16/02/2016 | https://clinicaltrials.gov/study/NCT02618434 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 16/02/2016 | https://clinicaltrials.gov/study/NCT02618434 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 25/01/2016 | https://clinicaltrials.gov/study/NCT02618408 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 25/01/2016 | https://clinicaltrials.gov/study/NCT02618408 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 25/01/2016 | https://clinicaltrials.gov/study/NCT02618408 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 25/01/2016 | https://clinicaltrials.gov/study/NCT02618408 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 25/01/2016 | https://clinicaltrials.gov/study/NCT02618408 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | MOLINDONE | targetBased | 3 | Completed | 25/01/2016 | https://clinicaltrials.gov/study/NCT02618408 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | HALOPERIDOL | targetBased | 4 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02343575 | 1 | LoF | protect | We did not recruit the research assistant and terminated the study |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2013 | https://clinicaltrials.gov/study/NCT02433041 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/06/2013 | https://clinicaltrials.gov/study/NCT01785290 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | HALOPERIDOL | targetBased | 4 | Active, not recruiting | 13/06/2018 | https://clinicaltrials.gov/study/NCT03392376 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | HALOPERIDOL | targetBased | 4 | Unknown status | 23/06/2017 | https://clinicaltrials.gov/study/NCT03199950 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01530308 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00097266 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00097266 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00097266 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00129220 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00129220 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00129220 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/06/2013 | https://clinicaltrials.gov/study/NCT01785290 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL | targetBased | 4 | Unknown status | 01/08/2008 | https://clinicaltrials.gov/study/NCT00838032 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7d1a9689-23c8-44ef-a474-8c607e13d794 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=12053bcb-dc5a-49a6-8e92-6804c07b0355 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7b01bd62-d0fa-4229-9a09-f90893dd6dbd | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL | targetBased | 4 | Terminated | 01/01/2003 | https://clinicaltrials.gov/study/NCT00419653 | 1 | LoF | protect | Recruitment issues |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=27cfe684-7d11-4f37-9c8b-b2bdd6b5348e | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e2eed126-cb82-42b1-9b48-9cbeb6873b50 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00129220 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01530308 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL | targetBased | 4 | Active, not recruiting | 13/06/2018 | https://clinicaltrials.gov/study/NCT03392376 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL | targetBased | 4 | Active, not recruiting | 13/06/2018 | https://clinicaltrials.gov/study/NCT03392376 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL | targetBased | 4 | Active, not recruiting | 13/06/2018 | https://clinicaltrials.gov/study/NCT03392376 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL | targetBased | 4 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT03489551 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | HALOPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD01 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | HALOPERIDOL | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | HALOPERIDOL | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | HALOPERIDOL | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL | targetBased | 4 | Terminated | 01/09/2017 | https://clinicaltrials.gov/study/NCT03246620 | 1 | LoF | protect | The study was terminated prematurely due to difficulties in patient recruitment and associated potential for selection bias. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/05/1996 | https://clinicaltrials.gov/study/NCT00253110 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | HALOPERIDOL | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00097266 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00129220 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | cannabis dependence | HALOPERIDOL | targetBased | 4 | Completed | 21/05/2017 | https://clinicaltrials.gov/study/NCT03056482 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | HALOPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD01 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | HALOPERIDOL | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00007774 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | HALOPERIDOL | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/05/1996 | https://clinicaltrials.gov/study/NCT00253110 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL | targetBased | 4 | Withdrawn | 01/04/2014 | https://clinicaltrials.gov/study/NCT02103881 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL | targetBased | 4 | Terminated | 30/09/2017 | https://clinicaltrials.gov/study/NCT03110900 | 1 | LoF | protect | Sponsor Withdrawal |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL | targetBased | 4 | Terminated | 30/09/2017 | https://clinicaltrials.gov/study/NCT03110900 | 1 | LoF | protect | Sponsor Withdrawal |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL | targetBased | 4 | Terminated | 30/09/2017 | https://clinicaltrials.gov/study/NCT03110900 | 1 | LoF | protect | Sponsor Withdrawal |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=153e747c-861d-44c4-aef6-6c49f53ca34a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=153e747c-861d-44c4-aef6-6c49f53ca34a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=153e747c-861d-44c4-aef6-6c49f53ca34a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c9d0d515-adb7-4f93-8363-0f11771321c9 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c9d0d515-adb7-4f93-8363-0f11771321c9 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c9d0d515-adb7-4f93-8363-0f11771321c9 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | HALOPERIDOL | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | HALOPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | HALOPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | HALOPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD01 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | HALOPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | HALOPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | HALOPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD01 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Tourette syndrome | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | HALOPERIDOL | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-operative delirium | HALOPERIDOL | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00250237 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | HALOPERIDOL | targetBased | 3 | Not yet recruiting | 28/03/2023 | https://clinicaltrials.gov/study/NCT05803642 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | HALOPERIDOL | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | HALOPERIDOL | targetBased | 4 | Terminated | 01/09/2017 | https://clinicaltrials.gov/study/NCT03246620 | 1 | LoF | protect | The study was terminated prematurely due to difficulties in patient recruitment and associated potential for selection bias. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | HALOPERIDOL | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | HALOPERIDOL | targetBased | 4 | Terminated | 30/09/2017 | https://clinicaltrials.gov/study/NCT03110900 | 1 | LoF | protect | Sponsor Withdrawal |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | HALOPERIDOL | targetBased | 4 | Withdrawn | 01/04/2014 | https://clinicaltrials.gov/study/NCT02103881 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | HALOPERIDOL | targetBased | 3 | Completed | 01/12/2012 | https://clinicaltrials.gov/study/NCT01750541 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e69578b5-3e98-4fc6-a5ad-61e8ec4cb8c1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c72c2366-7b40-4cd9-845d-4b3983e6141a | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c72c2366-7b40-4cd9-845d-4b3983e6141a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c72c2366-7b40-4cd9-845d-4b3983e6141a | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c72c2366-7b40-4cd9-845d-4b3983e6141a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c72c2366-7b40-4cd9-845d-4b3983e6141a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c72c2366-7b40-4cd9-845d-4b3983e6141a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | conduct disorder | HALOPERIDOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0027b8a3-73bf-4005-a7e3-b035f451a861 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety | HALOPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/05/1996 | https://clinicaltrials.gov/study/NCT00253110 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00007774 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00007774 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL | targetBased | 4 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00007774 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | THIORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC02 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety | THIORIDAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | THIORIDAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | MORPHINE | targetBased | 4 | Not yet recruiting | 06/06/2024 | https://clinicaltrials.gov/study/NCT06458400 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | MORPHINE | targetBased | 4 | Not yet recruiting | 06/06/2024 | https://clinicaltrials.gov/study/NCT06458400 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=533034fd-c8e7-495b-8874-0db41bd1e65a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=533034fd-c8e7-495b-8874-0db41bd1e65a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=83497476-dea9-57ec-e053-2991aa0a08c1 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=83497476-dea9-57ec-e053-2991aa0a08c1 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | MORPHINE | targetBased | 4 | Completed | 01/03/2013 | https://clinicaltrials.gov/study/NCT03078946 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | MORPHINE | targetBased | 4 | Completed | 01/03/2013 | https://clinicaltrials.gov/study/NCT03078946 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | MORPHINE | targetBased | 3 | Terminated | 20/05/2016 | https://clinicaltrials.gov/study/NCT03127800 | 0.7 | GoF | protect | Difficulties with recruitment |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | MORPHINE | targetBased | 3 | Terminated | 20/05/2016 | https://clinicaltrials.gov/study/NCT03127800 | 0.7 | GoF | protect | Difficulties with recruitment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | MORPHINE | targetBased | 3 | Unknown status | 01/05/2012 | https://clinicaltrials.gov/study/NCT01680939 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | MORPHINE | targetBased | 3 | Unknown status | 01/05/2012 | https://clinicaltrials.gov/study/NCT01680939 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE | targetBased | 4 | Terminated | 14/09/2016 | https://clinicaltrials.gov/study/NCT02741076 | 1 | GoF | protect | Inability to recruit sufficient no. of subjects over an acceptable time period |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE | targetBased | 4 | Terminated | 14/09/2016 | https://clinicaltrials.gov/study/NCT02741076 | 1 | GoF | protect | Inability to recruit sufficient no. of subjects over an acceptable time period |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE | targetBased | 4 | Recruiting | 13/12/2022 | https://clinicaltrials.gov/study/NCT05639712 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE | targetBased | 4 | Recruiting | 13/12/2022 | https://clinicaltrials.gov/study/NCT05639712 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE | targetBased | 3 | Terminated | 06/12/2019 | https://clinicaltrials.gov/study/NCT03948464 | 0.7 | GoF | protect | Study unable to proceed per protocol due to COVID-19 precautions |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE | targetBased | 3 | Terminated | 06/12/2019 | https://clinicaltrials.gov/study/NCT03948464 | 0.7 | GoF | protect | Study unable to proceed per protocol due to COVID-19 precautions |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE | targetBased | 3 | Active, not recruiting | 08/09/2020 | https://clinicaltrials.gov/study/NCT04214834 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE | targetBased | 3 | Active, not recruiting | 08/09/2020 | https://clinicaltrials.gov/study/NCT04214834 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | postpartum depression | MORPHINE | targetBased | 4 | Completed | 19/10/2019 | https://clinicaltrials.gov/study/NCT04017442 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | postpartum depression | MORPHINE | targetBased | 4 | Completed | 19/10/2019 | https://clinicaltrials.gov/study/NCT04017442 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | overdose | MORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=533034fd-c8e7-495b-8874-0db41bd1e65a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | overdose | MORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=533034fd-c8e7-495b-8874-0db41bd1e65a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | MORPHINE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01734551 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | MORPHINE | targetBased | 4 | Completed | 01/10/2016 | https://clinicaltrials.gov/study/NCT02851303 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | MORPHINE | targetBased | 4 | Completed | 01/10/2016 | https://clinicaltrials.gov/study/NCT02851303 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | MORPHINE | targetBased | 4 | Recruiting | 21/02/2018 | https://clinicaltrials.gov/study/NCT03092011 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | MORPHINE | targetBased | 4 | Recruiting | 21/02/2018 | https://clinicaltrials.gov/study/NCT03092011 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | MORPHINE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01804075 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | MORPHINE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01804075 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | MORPHINE | targetBased | 4 | Recruiting | 29/01/2024 | https://clinicaltrials.gov/study/NCT05905367 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | MORPHINE | targetBased | 4 | Recruiting | 29/01/2024 | https://clinicaltrials.gov/study/NCT05905367 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | sleep apnea | MORPHINE | targetBased | 4 | Completed | 01/11/2015 | https://clinicaltrials.gov/study/NCT02566226 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | sleep apnea | MORPHINE | targetBased | 4 | Completed | 01/11/2015 | https://clinicaltrials.gov/study/NCT02566226 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=73828e5b-6a29-21d9-e053-2991aa0acac4 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1cab3106-1064-4b42-892b-39f405d9e02f | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1cab3106-1064-4b42-892b-39f405d9e02f | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=df9801fc-03fe-41da-a6b3-0f76788217c9 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=df9801fc-03fe-41da-a6b3-0f76788217c9 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=160cd55a-a8ed-43f2-baf7-046d3c3b317f | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=160cd55a-a8ed-43f2-baf7-046d3c3b317f | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=44aeca03-3ac2-4d5b-91c2-9d0442086468 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=df9801fc-03fe-41da-a6b3-0f76788217c9 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=73828e5b-6a29-21d9-e053-2991aa0acac4 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1cab3106-1064-4b42-892b-39f405d9e02f | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=160cd55a-a8ed-43f2-baf7-046d3c3b317f | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=48a7e42b-934f-4ec6-e054-00144ff88e88 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=010905f9-3bcb-4b50-9fe8-a3ad0010f14c | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CHLORPROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CHLORPROMAZINE | targetBased | 4 | Terminated | 01/12/1994 | https://clinicaltrials.gov/study/NCT00169039 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CHLORPROMAZINE | targetBased | 3 | Completed | 01/04/2009 | https://clinicaltrials.gov/study/NCT00882518 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | Terminated | 01/12/1994 | https://clinicaltrials.gov/study/NCT00169039 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | Terminated | 01/12/1994 | https://clinicaltrials.gov/study/NCT00169039 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | Terminated | 01/12/1994 | https://clinicaltrials.gov/study/NCT00169039 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | neonatal abstinence syndrome | CHLORPROMAZINE | targetBased | 3 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT02810782 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | conduct disorder | CHLORPROMAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9575c766-3758-6f33-e053-2995a90ae6b1 | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/07/2011 | https://clinicaltrials.gov/study/NCT01374763 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/07/2007 | https://clinicaltrials.gov/study/NCT00684073 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/nyxoid | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT02038790 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00605033 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Withdrawn | 01/11/2009 | https://clinicaltrials.gov/study/NCT01015066 | 1 | LoF | protect | Study personnel left institution, anticipated funding did not occur |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Terminated | 01/11/2018 | https://clinicaltrials.gov/study/NCT03711318 | 0.7 | LoF | protect | continuing study was no longer feasible |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Terminated | 01/11/2018 | https://clinicaltrials.gov/study/NCT03711318 | 0.7 | LoF | protect | continuing study was no longer feasible |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Completed | 01/04/1996 | https://clinicaltrials.gov/study/NCT00015171 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Completed | 01/04/1996 | https://clinicaltrials.gov/study/NCT00015171 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALOXONE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00015340 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALOXONE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00015340 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALOXONE | targetBased | 3 | Completed | 15/05/2018 | https://clinicaltrials.gov/study/NCT03518021 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALOXONE | targetBased | 3 | Completed | 15/05/2018 | https://clinicaltrials.gov/study/NCT03518021 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Completed | 15/07/2019 | https://clinicaltrials.gov/study/NCT03908437 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Withdrawn | 30/11/2018 | https://clinicaltrials.gov/study/NCT03740243 | 1 | LoF | protect | No enrollment |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Recruiting | 03/11/2020 | https://clinicaltrials.gov/study/NCT04375033 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Recruiting | 01/12/2023 | https://clinicaltrials.gov/study/NCT05944952 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Not yet recruiting | 01/01/2020 | https://clinicaltrials.gov/study/NCT04091009 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 3 | Recruiting | 09/01/2024 | https://clinicaltrials.gov/study/NCT06089707 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Completed | 01/11/2020 | https://clinicaltrials.gov/study/NCT04283500 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | NALOXONE | targetBased | 3 | Completed | 15/05/2018 | https://clinicaltrials.gov/study/NCT03518021 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | NALOXONE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00015340 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Completed | 01/04/1996 | https://clinicaltrials.gov/study/NCT00015171 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | NALOXONE | targetBased | 3 | Terminated | 01/11/2018 | https://clinicaltrials.gov/study/NCT03711318 | 0.7 | LoF | protect | continuing study was no longer feasible |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | overdose | NALOXONE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05876572 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | morphine dependence | NALOXONE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | morphine dependence | NALOXONE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=236349ef-2cb5-47ca-a3a5-99534c3a4996 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=236349ef-2cb5-47ca-a3a5-99534c3a4996 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=784a0e98-c2d6-f845-e053-2991aa0ac4b4 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=784a0e98-c2d6-f845-e053-2991aa0ac4b4 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9be31bdf-e220-2978-e053-2a95a90a03c6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9be31bdf-e220-2978-e053-2a95a90a03c6 | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | substance withdrawal syndrome | NALOXONE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | substance withdrawal syndrome | NALOXONE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Withdrawn | 01/06/2023 | https://clinicaltrials.gov/study/NCT05808881 | 1 | LoF | protect | Due to changes in research objectives and methodological approach. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00015340 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00015340 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00605033 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE | targetBased | 4 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00605033 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | overdose | NALOXONE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05876572 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | overdose | NALOXONE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05876572 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Completed | 01/11/2020 | https://clinicaltrials.gov/study/NCT04283500 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Completed | 15/07/2019 | https://clinicaltrials.gov/study/NCT03908437 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Completed | 15/07/2019 | https://clinicaltrials.gov/study/NCT03908437 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Withdrawn | 30/11/2018 | https://clinicaltrials.gov/study/NCT03740243 | 1 | LoF | protect | No enrollment |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Withdrawn | 30/11/2018 | https://clinicaltrials.gov/study/NCT03740243 | 1 | LoF | protect | No enrollment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Not yet recruiting | 01/01/2020 | https://clinicaltrials.gov/study/NCT04091009 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALOXONE | targetBased | 4 | Not yet recruiting | 01/01/2020 | https://clinicaltrials.gov/study/NCT04091009 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | NALOXONE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | NALOXONE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | NALOXONE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | NALOXONE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | morphine dependence | NALOXONE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | morphine dependence | NALOXONE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | morphine dependence | NALOXONE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | morphine dependence | NALOXONE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | unipolar depression | NALOXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=784a0e98-c2d6-f845-e053-2991aa0ac4b4 | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | unipolar depression | NALOXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=236349ef-2cb5-47ca-a3a5-99534c3a4996 | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | unipolar depression | NALOXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9be31bdf-e220-2978-e053-2a95a90a03c6 | 1 | LoF | protect | |||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE | targetBased | 4 | Completed | 17/07/2018 | https://clinicaltrials.gov/study/NCT03418831 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE | targetBased | 4 | Completed | 01/08/2006 | https://clinicaltrials.gov/study/NCT00361543 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE | targetBased | 3 | Completed | 01/07/2011 | https://clinicaltrials.gov/study/NCT01573637 | 0.7 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01280305 | 0.7 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE | targetBased | 4 | Completed | 01/04/2011 | https://clinicaltrials.gov/study/NCT02354001 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE | targetBased | 4 | Completed | 01/01/2012 | https://clinicaltrials.gov/study/NCT01481883 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE | targetBased | 4 | Completed | 01/06/2004 | https://clinicaltrials.gov/study/NCT01041092 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | depressive disorder | RALOXIFENE | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00030147 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | depressive disorder | RALOXIFENE | targetBased | 4 | Unknown status | 01/01/2017 | https://clinicaltrials.gov/study/NCT03006003 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizoaffective disorder | RALOXIFENE | targetBased | 4 | Completed | 01/08/2006 | https://clinicaltrials.gov/study/NCT00361543 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizoaffective disorder | RALOXIFENE | targetBased | 4 | Completed | 01/04/2011 | https://clinicaltrials.gov/study/NCT02354001 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizoaffective disorder | RALOXIFENE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01280305 | 0.7 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizoaffective disorder | RALOXIFENE | targetBased | 4 | Completed | 01/01/2012 | https://clinicaltrials.gov/study/NCT01481883 | 1 | protect | ||
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | bipolar disorder | TAMOXIFEN | targetBased | 3 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00411203 | 0.7 | protect | ||
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | bipolar disorder | TAMOXIFEN | targetBased | 3 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00411203 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | drug dependence | BROMOCRIPTINE | targetBased | 4 | Withdrawn | 01/07/2013 | https://clinicaltrials.gov/study/NCT02929485 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | drug dependence | BROMOCRIPTINE | targetBased | 4 | Withdrawn | 01/07/2013 | https://clinicaltrials.gov/study/NCT02929485 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | drug dependence | BROMOCRIPTINE | targetBased | 4 | Withdrawn | 01/07/2013 | https://clinicaltrials.gov/study/NCT02929485 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | drug dependence | BROMOCRIPTINE | targetBased | 4 | Withdrawn | 01/07/2013 | https://clinicaltrials.gov/study/NCT02929485 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | drug dependence | BROMOCRIPTINE | targetBased | 4 | Withdrawn | 01/07/2013 | https://clinicaltrials.gov/study/NCT02929485 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | drug dependence | BROMOCRIPTINE | targetBased | 4 | Withdrawn | 01/07/2013 | https://clinicaltrials.gov/study/NCT02929485 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | drug dependence | BROMOCRIPTINE | targetBased | 4 | Withdrawn | 01/07/2013 | https://clinicaltrials.gov/study/NCT02929485 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | drug dependence | BROMOCRIPTINE | targetBased | 4 | Withdrawn | 01/07/2013 | https://clinicaltrials.gov/study/NCT02929485 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | drug dependence | BROMOCRIPTINE | targetBased | 4 | Withdrawn | 01/07/2013 | https://clinicaltrials.gov/study/NCT02929485 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | RISPERIDONE | targetBased | 4 | Terminated | 01/01/2008 | https://clinicaltrials.gov/study/NCT00622011 | 1 | LoF | protect | inadequate participant |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00095134 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00044681 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00266552 | 0.7 | LoF | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00266552 | 0.7 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00266552 | 0.7 | LoF | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00266552 | 0.7 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00250354 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00250354 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00250354 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00250354 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00250354 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00250354 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00208182 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1522f0b9-2bbc-4785-bada-fa6ae7986bb4 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a6347895-5f16-43b4-92a0-b9904ac81937 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a6347895-5f16-43b4-92a0-b9904ac81937 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a6347895-5f16-43b4-92a0-b9904ac81937 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a6347895-5f16-43b4-92a0-b9904ac81937 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a6347895-5f16-43b4-92a0-b9904ac81937 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a6347895-5f16-43b4-92a0-b9904ac81937 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00250354 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/12/2001 | https://clinicaltrials.gov/study/NCT00236444 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00266552 | 0.7 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/01/2002 | https://clinicaltrials.gov/study/NCT00236470 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Rett syndrome | RISPERIDONE | targetBased | 3 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00261508 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | RISPERIDONE | targetBased | 4 | Terminated | 01/01/2008 | https://clinicaltrials.gov/study/NCT00622011 | 1 | LoF | protect | inadequate participant |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | RISPERIDONE | targetBased | 4 | Terminated | 01/01/2008 | https://clinicaltrials.gov/study/NCT00622011 | 1 | LoF | protect | inadequate participant |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | RISPERIDONE | targetBased | 4 | Terminated | 01/01/2008 | https://clinicaltrials.gov/study/NCT00622011 | 1 | LoF | protect | inadequate participant |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | RISPERIDONE | targetBased | 4 | Terminated | 01/01/2008 | https://clinicaltrials.gov/study/NCT00622011 | 1 | LoF | protect | inadequate participant |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | RISPERIDONE | targetBased | 4 | Terminated | 01/01/2008 | https://clinicaltrials.gov/study/NCT00622011 | 1 | LoF | protect | inadequate participant |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | RISPERIDONE | targetBased | 4 | Terminated | 01/01/2008 | https://clinicaltrials.gov/study/NCT00622011 | 1 | LoF | protect | inadequate participant |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Asperger syndrome | RISPERIDONE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00352196 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Asperger syndrome | RISPERIDONE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00352196 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Asperger syndrome | RISPERIDONE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00352196 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Asperger syndrome | RISPERIDONE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00352196 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Asperger syndrome | RISPERIDONE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00352196 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Asperger syndrome | RISPERIDONE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00352196 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Asperger syndrome | RISPERIDONE | targetBased | 3 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00261508 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Borderline personality disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00204347 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ea914046-6cc2-4c7b-b12b-76c31bb18def | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | RISPERIDONE | targetBased | 4 | Completed | 01/09/1999 | https://clinicaltrials.gov/study/NCT00308360 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5b597f75-e579-438d-b162-c906c3b01088 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | RISPERIDONE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00130923 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2e5c6b7f-1d57-4114-9067-79dca009c4cc | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | RISPERIDONE | targetBased | 4 | Unknown status | 01/07/2009 | https://clinicaltrials.gov/study/NCT00937261 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | RISPERIDONE | targetBased | 4 | Terminated | 01/08/2007 | https://clinicaltrials.gov/study/NCT00498004 | 1 | LoF | protect | difficult to recruit subject |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5958bb43-6967-4f15-9bd1-7f06340527ff | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d072638f-70d6-4ce9-a0d4-16db4b31d824 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d072638f-70d6-4ce9-a0d4-16db4b31d824 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d072638f-70d6-4ce9-a0d4-16db4b31d824 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d072638f-70d6-4ce9-a0d4-16db4b31d824 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d072638f-70d6-4ce9-a0d4-16db4b31d824 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d072638f-70d6-4ce9-a0d4-16db4b31d824 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Terminated | 01/07/2012 | https://clinicaltrials.gov/study/NCT01813643 | 0.5 | LoF | protect | Effects of aripiprazole was not obvious and showed adverse reaction obviously |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | RISPERIDONE | targetBased | 3 | Completed | 01/11/1999 | https://clinicaltrials.gov/study/NCT00253136 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | RISPERIDONE | targetBased | 3 | Completed | 01/01/2000 | https://clinicaltrials.gov/study/NCT00249223 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | RISPERIDONE | targetBased | 3 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00236457 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | RISPERIDONE | targetBased | 3 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00034762 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00369239 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00108368 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00266552 | 0.7 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | conduct disorder | RISPERIDONE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00250354 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00249158 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00249158 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00249158 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00249158 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00253123 | 0.7 | LoF | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00253123 | 0.7 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00253123 | 0.7 | LoF | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00253123 | 0.7 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00253123 | 0.7 | LoF | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00253123 | 0.7 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment resistant depression | RISPERIDONE | targetBased | 4 | Withdrawn | 01/05/2004 | https://clinicaltrials.gov/study/NCT00178854 | 1 | LoF | protect | failed recruitment efforts |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | RISPERIDONE | targetBased | 3 | Terminated | 01/03/2002 | https://clinicaltrials.gov/study/NCT00287742 | 0.7 | LoF | protect | A decision was made to discontinue the study due to a change in the strategic direction of the company. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | RISPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | RISPERIDONE | targetBased | 3 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00034762 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | RISPERIDONE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | RISPERIDONE | targetBased | 3 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00249158 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00253123 | 0.7 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | RISPERIDONE | targetBased | 3 | Completed | 01/04/1995 | https://clinicaltrials.gov/study/NCT00249145 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | RISPERIDONE | targetBased | 4 | Completed | 01/08/2008 | https://clinicaltrials.gov/study/NCT00594269 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00095134 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00095134 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00095134 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00095134 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00044681 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00044681 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00044681 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00044681 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00044681 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00044681 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Asperger syndrome | RISPERIDONE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00352196 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Asperger syndrome | RISPERIDONE | targetBased | 3 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00261508 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Rett syndrome | RISPERIDONE | targetBased | 3 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00261508 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Rett syndrome | RISPERIDONE | targetBased | 3 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00261508 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Rett syndrome | RISPERIDONE | targetBased | 3 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00261508 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Rett syndrome | RISPERIDONE | targetBased | 3 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00261508 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Rett syndrome | RISPERIDONE | targetBased | 3 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00261508 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Rett syndrome | RISPERIDONE | targetBased | 3 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00261508 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00208182 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00208182 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00208182 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00208182 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00208182 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00208182 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | RISPERIDONE | targetBased | 4 | Terminated | 01/03/2005 | https://clinicaltrials.gov/study/NCT00203723 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | alcohol abuse | RISPERIDONE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00130923 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00086112 | 0.7 | LoF | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00086112 | 0.7 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00086112 | 0.7 | LoF | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00086112 | 0.7 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00086112 | 0.7 | LoF | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00086112 | 0.7 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | RISPERIDONE | targetBased | 4 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00790075 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | RISPERIDONE | targetBased | 4 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00790075 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | RISPERIDONE | targetBased | 4 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00790075 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | RISPERIDONE | targetBased | 4 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00790075 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | RISPERIDONE | targetBased | 4 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00790075 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | RISPERIDONE | targetBased | 4 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00790075 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00325689 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00337662 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00337662 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00337662 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00337662 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00337662 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00337662 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b6b3577f-7ebb-401f-b7e0-b707b35e09ed | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=246866c2-31f0-4770-8fa4-22e5b3556347 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=275e99fc-7977-4d72-9294-1d1348188798 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | aggressive behavior | RISPERIDONE | targetBased | 4 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00297739 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b6a3d727-030c-407a-9bbf-34da8ce54fa6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=23993d21-80bf-41c4-b57d-88a620173b6b | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | aggressive behavior | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1522f0b9-2bbc-4785-bada-fa6ae7986bb4 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | RISPERIDONE | targetBased | 3 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00177164 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5e1eba05-036a-440f-85e3-a24b7ff3eb55 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=51b65970-02e6-4558-a4b3-38e56e0c073c | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bb34ee82-d2c2-43b8-ba21-2825c0954691 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | RISPERIDONE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT01977300 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | RISPERIDONE | targetBased | 3 | Terminated | 01/04/2009 | https://clinicaltrials.gov/study/NCT00857818 | 0.7 | LoF | protect | Slow Accrual |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=89595dbd-2722-41f2-88ae-8c43769702bf | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=daf11e04-d69c-4aaa-80e6-a4bac692736c | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e5ec2af6-7777-4dc2-9cea-eefc2629d5ad | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=82effea8-5782-4aa5-969e-b635423ae3c6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e344c976-fc8b-42b4-933c-2d63488182f0 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5e1eba05-036a-440f-85e3-a24b7ff3eb55 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f06a91eb-5aa0-4722-8644-c56bbd975f02 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dd1c68bd-abba-45b3-9c3c-586d77c18853 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | RISPERIDONE | targetBased | 4 | Completed | 01/06/2001 | https://clinicaltrials.gov/study/NCT00182013 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | RISPERIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance dependence | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance dependence | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance dependence | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance dependence | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance dependence | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance dependence | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism spectrum disorder | RISPERIDONE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT05146245 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Williams syndrome | RISPERIDONE | targetBased | 4 | Recruiting | 01/05/2001 | https://clinicaltrials.gov/study/NCT00768820 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Williams syndrome | RISPERIDONE | targetBased | 4 | Recruiting | 01/05/2001 | https://clinicaltrials.gov/study/NCT00768820 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Williams syndrome | RISPERIDONE | targetBased | 4 | Recruiting | 01/05/2001 | https://clinicaltrials.gov/study/NCT00768820 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Williams syndrome | RISPERIDONE | targetBased | 4 | Recruiting | 01/05/2001 | https://clinicaltrials.gov/study/NCT00768820 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Williams syndrome | RISPERIDONE | targetBased | 4 | Recruiting | 01/05/2001 | https://clinicaltrials.gov/study/NCT00768820 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Williams syndrome | RISPERIDONE | targetBased | 4 | Recruiting | 01/05/2001 | https://clinicaltrials.gov/study/NCT00768820 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/01/2002 | https://clinicaltrials.gov/study/NCT00236470 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/01/2002 | https://clinicaltrials.gov/study/NCT00236470 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/01/2002 | https://clinicaltrials.gov/study/NCT00236470 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/01/2002 | https://clinicaltrials.gov/study/NCT00236470 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/12/2001 | https://clinicaltrials.gov/study/NCT00236444 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/12/2001 | https://clinicaltrials.gov/study/NCT00236444 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/12/2001 | https://clinicaltrials.gov/study/NCT00236444 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/12/2001 | https://clinicaltrials.gov/study/NCT00236444 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/12/2001 | https://clinicaltrials.gov/study/NCT00236444 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Oppositional defiant disorder | RISPERIDONE | targetBased | 3 | Completed | 01/12/2001 | https://clinicaltrials.gov/study/NCT00236444 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | RISPERIDONE | targetBased | 4 | Terminated | 11/05/2023 | https://clinicaltrials.gov/study/NCT05890768 | 1 | LoF | protect | PI was unable to meet 1 year recruitment goal |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | RISPERIDONE | targetBased | 4 | Terminated | 01/07/2013 | https://clinicaltrials.gov/study/NCT01844700 | 0.5 | LoF | protect | very slow recruitment, no sufficient results |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | RISPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX08 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance abuse | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance abuse | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance abuse | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance abuse | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance abuse | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance abuse | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00253123 | 0.7 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | 01/03/1998 | https://clinicaltrials.gov/study/NCT00249158 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | vascular dementia | RISPERIDONE | targetBased | 3 | Completed | 01/04/1995 | https://clinicaltrials.gov/study/NCT00249145 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/05/1996 | https://clinicaltrials.gov/study/NCT00253110 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00369239 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/01/2007 | https://clinicaltrials.gov/study/NCT00423878 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00190749 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00215579 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Terminated | 01/04/2013 | https://clinicaltrials.gov/study/NCT01913327 | 1 | LoF | protect | Insufficient Funds and Inadequate Subject Recruitment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | RISPERIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | substance dependence | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | RISPERIDONE | targetBased | 3 | Unknown status | 01/02/2003 | https://clinicaltrials.gov/study/NCT00174577 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | RISPERIDONE | targetBased | 4 | Terminated | 01/03/2005 | https://clinicaltrials.gov/study/NCT00203723 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | RISPERIDONE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | RISPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00044681 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/02/2008 | https://clinicaltrials.gov/study/NCT00640562 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | RISPERIDONE | targetBased | 3 | Terminated | 01/09/2001 | https://clinicaltrials.gov/study/NCT00174590 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | RISPERIDONE | targetBased | 3 | Completed | 01/06/2004 | https://clinicaltrials.gov/study/NCT00167154 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | RISPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX08 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | RISPERIDONE | targetBased | 4 | Terminated | 11/05/2023 | https://clinicaltrials.gov/study/NCT05890768 | 1 | LoF | protect | PI was unable to meet 1 year recruitment goal |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | RISPERIDONE | targetBased | 4 | Terminated | 11/05/2023 | https://clinicaltrials.gov/study/NCT05890768 | 1 | LoF | protect | PI was unable to meet 1 year recruitment goal |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | RISPERIDONE | targetBased | 4 | Terminated | 11/05/2023 | https://clinicaltrials.gov/study/NCT05890768 | 1 | LoF | protect | PI was unable to meet 1 year recruitment goal |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | RISPERIDONE | targetBased | 4 | Terminated | 11/05/2023 | https://clinicaltrials.gov/study/NCT05890768 | 1 | LoF | protect | PI was unable to meet 1 year recruitment goal |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | RISPERIDONE | targetBased | 4 | Terminated | 11/05/2023 | https://clinicaltrials.gov/study/NCT05890768 | 1 | LoF | protect | PI was unable to meet 1 year recruitment goal |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | RISPERIDONE | targetBased | 4 | Terminated | 11/05/2023 | https://clinicaltrials.gov/study/NCT05890768 | 1 | LoF | protect | PI was unable to meet 1 year recruitment goal |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | RISPERIDONE | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00277654 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | RISPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | RISPERIDONE | targetBased | 3 | Terminated | 01/09/2017 | https://clinicaltrials.gov/study/NCT03227562 | 0.7 | LoF | protect | not enough patient |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | RISPERIDONE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00086112 | 0.7 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | substance abuse | RISPERIDONE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | attention deficit hyperactivity disorder | RISPERIDONE | targetBased | 4 | Completed | 01/08/2008 | https://clinicaltrials.gov/study/NCT00796302 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | attention deficit hyperactivity disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/11/2008 | https://clinicaltrials.gov/study/NCT00794625 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f11dae15-b057-4258-9229-3819d0c980fe | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1097d343-413d-49fc-8bc9-34a1fdc0b643 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1cd2c55a-f30a-4a3f-92d8-baa3886b3a8b | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0dc12b44-73f8-416c-88bb-0b11b3e35458 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b939e746-6b5f-ae82-c5f4-79cfdf6253ea | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7073b706-1946-4ff2-8788-fb9452a59cae | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | RISPERIDONE | targetBased | 4 | Completed | 01/07/2011 | https://clinicaltrials.gov/study/NCT01333072 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Terminated | 01/07/2012 | https://clinicaltrials.gov/study/NCT01813643 | 0.5 | LoF | protect | Effects of aripiprazole was not obvious and showed adverse reaction obviously |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Terminated | 01/07/2012 | https://clinicaltrials.gov/study/NCT01813643 | 0.5 | LoF | protect | Effects of aripiprazole was not obvious and showed adverse reaction obviously |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | RISPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Williams syndrome | RISPERIDONE | targetBased | 4 | Recruiting | 01/05/2001 | https://clinicaltrials.gov/study/NCT00768820 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | RISPERIDONE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | RISPERIDONE | targetBased | 4 | Completed | 01/08/2008 | https://clinicaltrials.gov/study/NCT00594269 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | RISPERIDONE | targetBased | 4 | Completed | 01/08/2008 | https://clinicaltrials.gov/study/NCT00594269 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | RISPERIDONE | targetBased | 4 | Completed | 01/08/2008 | https://clinicaltrials.gov/study/NCT00594269 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | RISPERIDONE | targetBased | 4 | Completed | 01/08/2008 | https://clinicaltrials.gov/study/NCT00594269 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | RISPERIDONE | targetBased | 4 | Completed | 01/08/2008 | https://clinicaltrials.gov/study/NCT00594269 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | RISPERIDONE | targetBased | 4 | Completed | 01/08/2008 | https://clinicaltrials.gov/study/NCT00594269 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | RISPERIDONE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT05146245 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | RISPERIDONE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT05146245 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism spectrum disorder | RISPERIDONE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT05146245 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism spectrum disorder | RISPERIDONE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT05146245 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | RISPERIDONE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT05146245 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | RISPERIDONE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT05146245 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bb34ee82-d2c2-43b8-ba21-2825c0954691 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=89595dbd-2722-41f2-88ae-8c43769702bf | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=89595dbd-2722-41f2-88ae-8c43769702bf | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=89595dbd-2722-41f2-88ae-8c43769702bf | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=89595dbd-2722-41f2-88ae-8c43769702bf | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=89595dbd-2722-41f2-88ae-8c43769702bf | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=89595dbd-2722-41f2-88ae-8c43769702bf | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol abuse | RISPERIDONE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00130923 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol abuse | RISPERIDONE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00130923 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol abuse | RISPERIDONE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00130923 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol abuse | RISPERIDONE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00130923 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol abuse | RISPERIDONE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00130923 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol abuse | RISPERIDONE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00130923 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | RISPERIDONE | targetBased | 4 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00790075 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1ecf6682-7ad4-4320-ab19-f17dfc5241f8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5f0bdf9d-fa78-45e8-913a-81beff57cf34 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5f0bdf9d-fa78-45e8-913a-81beff57cf34 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5f0bdf9d-fa78-45e8-913a-81beff57cf34 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5f0bdf9d-fa78-45e8-913a-81beff57cf34 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5f0bdf9d-fa78-45e8-913a-81beff57cf34 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5f0bdf9d-fa78-45e8-913a-81beff57cf34 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | RISPERIDONE | targetBased | 4 | Completed | 01/08/2008 | https://clinicaltrials.gov/study/NCT00796302 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/11/2008 | https://clinicaltrials.gov/study/NCT00794625 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/11/2008 | https://clinicaltrials.gov/study/NCT00794625 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/11/2008 | https://clinicaltrials.gov/study/NCT00794625 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/11/2008 | https://clinicaltrials.gov/study/NCT00794625 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/11/2008 | https://clinicaltrials.gov/study/NCT00794625 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | RISPERIDONE | targetBased | 4 | Unknown status | 01/11/2008 | https://clinicaltrials.gov/study/NCT00794625 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cd742c16-c003-4c4c-8fa0-a3b4d0158383 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7a3c4f98-753f-4930-8b97-24d2d40ecfa7 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7a3c4f98-753f-4930-8b97-24d2d40ecfa7 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7a3c4f98-753f-4930-8b97-24d2d40ecfa7 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7a3c4f98-753f-4930-8b97-24d2d40ecfa7 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7a3c4f98-753f-4930-8b97-24d2d40ecfa7 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | RISPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7a3c4f98-753f-4930-8b97-24d2d40ecfa7 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | RISPERIDONE | targetBased | 4 | Withdrawn | 01/05/2004 | https://clinicaltrials.gov/study/NCT00178854 | 1 | LoF | protect | failed recruitment efforts |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | RISPERIDONE | targetBased | 4 | Withdrawn | 01/05/2004 | https://clinicaltrials.gov/study/NCT00178854 | 1 | LoF | protect | failed recruitment efforts |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | RISPERIDONE | targetBased | 4 | Withdrawn | 01/05/2004 | https://clinicaltrials.gov/study/NCT00178854 | 1 | LoF | protect | failed recruitment efforts |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | RISPERIDONE | targetBased | 4 | Withdrawn | 01/05/2004 | https://clinicaltrials.gov/study/NCT00178854 | 1 | LoF | protect | failed recruitment efforts |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | RISPERIDONE | targetBased | 4 | Withdrawn | 01/05/2004 | https://clinicaltrials.gov/study/NCT00178854 | 1 | LoF | protect | failed recruitment efforts |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | RISPERIDONE | targetBased | 4 | Withdrawn | 01/05/2004 | https://clinicaltrials.gov/study/NCT00178854 | 1 | LoF | protect | failed recruitment efforts |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00204347 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00204347 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00204347 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00204347 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00204347 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | RISPERIDONE | targetBased | 4 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00204347 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE | targetBased | 4 | Completed | 01/01/2014 | https://clinicaltrials.gov/study/NCT03017430 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | depressive disorder | PINDOLOL | targetBased | 4 | Withdrawn | 01/01/2004 | https://clinicaltrials.gov/study/NCT00221494 | 1 | GoF | protect | PI move |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | AMPHETAMINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bb12811f-4cce-4010-aa48-d17c46ca1d3a | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | AMPHETAMINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | AMPHETAMINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f469fb38-0380-4621-9db3-a4f429126156 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1e25f905-6c0b-4b19-a3b6-b2a386afa1c3 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f469fb38-0380-4621-9db3-a4f429126156 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE SULFATE | targetBased | 3 | Completed | 13/09/2018 | https://clinicaltrials.gov/study/NCT03659929 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE SULFATE | targetBased | 3 | Completed | 27/01/2005 | https://clinicaltrials.gov/study/NCT00150579 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE SULFATE | targetBased | 3 | Completed | 10/03/2005 | https://clinicaltrials.gov/study/NCT00152035 | 0.7 | protect | ||
HCS assay for microtubule stabilizers | TUBB | TUBB | Tubulin beta chain | Anorexia | DOCETAXEL | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00040885 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | SERTINDOLE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | SERTINDOLE | targetBased | 4 | Unknown status | 01/10/2008 | https://clinicaltrials.gov/study/NCT00480844 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | SERTINDOLE | targetBased | 3 | Completed | 01/10/2006 | https://clinicaltrials.gov/study/NCT00759421 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | SERTINDOLE | targetBased | 3 | Completed | 01/03/2007 | https://clinicaltrials.gov/study/NCT00759460 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | SERTINDOLE | targetBased | 3 | Completed | 01/07/2002 | https://clinicaltrials.gov/study/NCT00856583 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | SERTINDOLE | targetBased | 4 | Terminated | 01/07/2008 | https://clinicaltrials.gov/study/NCT02021201 | 1 | LoF | protect | No suitable patients could be recruited in the available time period |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | SERTINDOLE | targetBased | 4 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00763438 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SERTINDOLE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SERTINDOLE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SERTINDOLE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SERTINDOLE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SERTINDOLE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | SERTINDOLE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | SERTINDOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE03 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | SERTINDOLE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | SERTINDOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | SERTINDOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | SERTINDOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE03 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | SERTINDOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | SERTINDOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | SERTINDOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE03 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | SERTINDOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | SERTINDOLE | targetBased | 4 | Terminated | 01/07/2008 | https://clinicaltrials.gov/study/NCT02021201 | 1 | LoF | protect | No suitable patients could be recruited in the available time period |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | SERTINDOLE | targetBased | 4 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00763438 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | SERTINDOLE | targetBased | 4 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00763438 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | SERTINDOLE | targetBased | 4 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00763438 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | SERTINDOLE | targetBased | 4 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00763438 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | SERTINDOLE | targetBased | 4 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00763438 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | SERTINDOLE | targetBased | 4 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00763438 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | cocaine dependence | PERGOLIDE | targetBased | 3 | Completed | 01/02/1996 | https://clinicaltrials.gov/study/NCT00000248 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01464229 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ILOPERIDONE | targetBased | 3 | Unknown status | 01/11/2013 | https://clinicaltrials.gov/study/NCT02453893 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ILOPERIDONE | targetBased | 3 | Completed | 01/02/2011 | https://clinicaltrials.gov/study/NCT01291511 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=43452bf8-76e7-47a9-a5d8-41fe84d061f0 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ILOPERIDONE | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00254202 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ILOPERIDONE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01207414 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6f17cc91-86b3-42e3-9bf2-935dd360c3eb | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=33f60b40-3fca-11de-8f56-0002a5d5c51b | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ILOPERIDONE | targetBased | 4 | Terminated | 01/04/2012 | https://clinicaltrials.gov/study/NCT01929889 | 1 | LoF | protect | Low recruitment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT02413918 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT02413918 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT02413918 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT02413918 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT02413918 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT02413918 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01464229 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01464229 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01464229 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01464229 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01464229 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01464229 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ILOPERIDONE | targetBased | 4 | Terminated | 01/04/2012 | https://clinicaltrials.gov/study/NCT01929889 | 1 | LoF | protect | Low recruitment |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ILOPERIDONE | targetBased | 4 | Terminated | 01/04/2012 | https://clinicaltrials.gov/study/NCT01929889 | 1 | LoF | protect | Low recruitment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ILOPERIDONE | targetBased | 4 | Terminated | 01/04/2012 | https://clinicaltrials.gov/study/NCT01929889 | 1 | LoF | protect | Low recruitment |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ILOPERIDONE | targetBased | 4 | Terminated | 01/04/2012 | https://clinicaltrials.gov/study/NCT01929889 | 1 | LoF | protect | Low recruitment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ILOPERIDONE | targetBased | 4 | Terminated | 01/04/2012 | https://clinicaltrials.gov/study/NCT01929889 | 1 | LoF | protect | Low recruitment |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ILOPERIDONE | targetBased | 4 | Terminated | 01/04/2012 | https://clinicaltrials.gov/study/NCT01929889 | 1 | LoF | protect | Low recruitment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ILOPERIDONE | targetBased | 3 | Completed | 22/03/2021 | https://clinicaltrials.gov/study/NCT04819776 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT02413918 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ILOPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ILOPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX14 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ILOPERIDONE | targetBased | 4 | Terminated | 01/04/2012 | https://clinicaltrials.gov/study/NCT01929889 | 1 | LoF | protect | Low recruitment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ILOPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX14 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ILOPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX14 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ILOPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX14 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ILOPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX14 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ILOPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX14 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ILOPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX14 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ILOPERIDONE | targetBased | 3 | Completed | 22/03/2021 | https://clinicaltrials.gov/study/NCT04819776 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ILOPERIDONE | targetBased | 3 | Completed | 22/03/2021 | https://clinicaltrials.gov/study/NCT04819776 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ILOPERIDONE | targetBased | 3 | Completed | 22/03/2021 | https://clinicaltrials.gov/study/NCT04819776 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ILOPERIDONE | targetBased | 3 | Completed | 22/03/2021 | https://clinicaltrials.gov/study/NCT04819776 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ILOPERIDONE | targetBased | 3 | Completed | 22/03/2021 | https://clinicaltrials.gov/study/NCT04819776 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ILOPERIDONE | targetBased | 3 | Completed | 22/03/2021 | https://clinicaltrials.gov/study/NCT04819776 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6f17cc91-86b3-42e3-9bf2-935dd360c3eb | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=43452bf8-76e7-47a9-a5d8-41fe84d061f0 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=43452bf8-76e7-47a9-a5d8-41fe84d061f0 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=43452bf8-76e7-47a9-a5d8-41fe84d061f0 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=43452bf8-76e7-47a9-a5d8-41fe84d061f0 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=43452bf8-76e7-47a9-a5d8-41fe84d061f0 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ILOPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=43452bf8-76e7-47a9-a5d8-41fe84d061f0 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | NOMIFENSINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX04 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PROMAZINE | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00654576 | 1 | LoF | protect | |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | TRPV1 | Transient receptor potential cation channel subfamily V member 1 | opioid dependence | ACETAMINOPHEN | targetBased | 4 | Completed | 01/08/2019 | https://clinicaltrials.gov/study/NCT04015908 | 1 | protect | ||
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | TRPV1 | Transient receptor potential cation channel subfamily V member 1 | opioid dependence | ACETAMINOPHEN | targetBased | 4 | Terminated | 17/05/2021 | https://clinicaltrials.gov/study/NCT04766996 | 1 | protect | Loss of surgery team member deemed the study procedures impossible to achieve, and no replacement could be found in a timely manner to complete trial as initially planned. | |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | TRPV1 | Transient receptor potential cation channel subfamily V member 1 | opioid dependence | ACETAMINOPHEN | targetBased | 4 | Terminated | 01/11/2019 | https://clinicaltrials.gov/study/NCT03732469 | 1 | protect | Significant change in our clinic structure prevented continued recruitment of patients to the study | |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | TRPV1 | Transient receptor potential cation channel subfamily V member 1 | opioid dependence | ACETAMINOPHEN | targetBased | 4 | Completed | 30/01/2018 | https://clinicaltrials.gov/study/NCT03457116 | 1 | protect | ||
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | TRPV1 | Transient receptor potential cation channel subfamily V member 1 | mental or behavioural disorder | ACETAMINOPHEN | targetBased | 4 | Unknown status | 20/11/2018 | https://clinicaltrials.gov/study/NCT03830398 | 1 | protect | ||
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | TRPV1 | Transient receptor potential cation channel subfamily V member 1 | alcohol dependence | ACETAMINOPHEN | targetBased | 4 | Completed | 01/11/2004 | https://clinicaltrials.gov/study/NCT00427206 | 1 | protect | ||
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | TRPV1 | Transient receptor potential cation channel subfamily V member 1 | alcohol dependence | ACETAMINOPHEN | targetBased | 4 | Completed | 01/01/2002 | https://clinicaltrials.gov/study/NCT00402571 | 1 | protect | ||
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | TRPV1 | Transient receptor potential cation channel subfamily V member 1 | delirium | ACETAMINOPHEN | targetBased | 4 | Completed | 01/10/2015 | https://clinicaltrials.gov/study/NCT02546765 | 1 | protect | ||
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | TRPV1 | Transient receptor potential cation channel subfamily V member 1 | delirium | ACETAMINOPHEN | targetBased | 3 | Recruiting | 06/06/2023 | https://clinicaltrials.gov/study/NCT05246644 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PERPHENAZINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PERPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PERPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PERPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB03 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PERPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PERPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PERPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | PERPHENAZINE | targetBased | 3 | Completed | 01/09/1995 | https://clinicaltrials.gov/study/NCT00009204 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PERPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=20e508cb-20ae-48dc-838a-abe61eb7c0ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PERPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0ebf4c11-1810-42f6-a8e3-071616e33d5d | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PERPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0ebf4c11-1810-42f6-a8e3-071616e33d5d | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PERPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0ebf4c11-1810-42f6-a8e3-071616e33d5d | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PERPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0ebf4c11-1810-42f6-a8e3-071616e33d5d | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PERPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0ebf4c11-1810-42f6-a8e3-071616e33d5d | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PERPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0ebf4c11-1810-42f6-a8e3-071616e33d5d | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA05 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA05 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA05 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA05 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA05 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | TRIFLUPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA05 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | ROPINIROLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00314821 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | ROPINIROLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00314821 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | ROPINIROLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00314821 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ROPINIROLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00314821 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ROPINIROLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00314821 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ROPINIROLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00314821 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ROPINIROLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00314821 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ROPINIROLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00314821 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ROPINIROLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00314821 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | major depressive disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | major depressive disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | major depressive disorder | ROPINIROLE | targetBased | 4 | Unknown status | 01/04/2003 | https://clinicaltrials.gov/study/NCT00335205 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | FENTANYL | targetBased | 4 | Withdrawn | 01/08/2017 | https://clinicaltrials.gov/study/NCT02119806 | 1 | GoF | protect | Study was never initiated. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | FENTANYL | targetBased | 4 | Unknown status | 01/02/2014 | https://clinicaltrials.gov/study/NCT02080169 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | FENTANYL | targetBased | 4 | Unknown status | 01/02/2014 | https://clinicaltrials.gov/study/NCT02080169 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | FENTANYL | targetBased | 4 | Unknown status | 01/12/2015 | https://clinicaltrials.gov/study/NCT02528513 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | FENTANYL | targetBased | 4 | Unknown status | 01/12/2015 | https://clinicaltrials.gov/study/NCT02528513 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | FENTANYL | targetBased | 4 | Unknown status | 01/07/2014 | https://clinicaltrials.gov/study/NCT02078583 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | FENTANYL | targetBased | 4 | Unknown status | 01/07/2014 | https://clinicaltrials.gov/study/NCT02078583 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | FENTANYL | targetBased | 3 | Completed | 01/03/2007 | https://clinicaltrials.gov/study/NCT00468052 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | FENTANYL | targetBased | 3 | Completed | 01/03/2007 | https://clinicaltrials.gov/study/NCT00468052 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | FENTANYL | targetBased | 4 | Terminated | 01/11/2019 | https://clinicaltrials.gov/study/NCT03732469 | 1 | GoF | protect | Significant change in our clinic structure prevented continued recruitment of patients to the study |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | FENTANYL | targetBased | 4 | Completed | 16/01/2019 | https://clinicaltrials.gov/study/NCT03809949 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | FENTANYL | targetBased | 4 | Completed | 16/01/2019 | https://clinicaltrials.gov/study/NCT03809949 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | FENTANYL | targetBased | 4 | Recruiting | 13/12/2022 | https://clinicaltrials.gov/study/NCT05639712 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | FENTANYL | targetBased | 4 | Recruiting | 13/12/2022 | https://clinicaltrials.gov/study/NCT05639712 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | FENTANYL | targetBased | 4 | Recruiting | 07/06/2023 | https://clinicaltrials.gov/study/NCT05980546 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | FENTANYL | targetBased | 4 | Recruiting | 07/06/2023 | https://clinicaltrials.gov/study/NCT05980546 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | FENTANYL | targetBased | 4 | Unknown status | 01/12/2018 | https://clinicaltrials.gov/study/NCT03666494 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | FENTANYL | targetBased | 4 | Unknown status | 01/12/2018 | https://clinicaltrials.gov/study/NCT03666494 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | FENTANYL | targetBased | 4 | Recruiting | 29/01/2024 | https://clinicaltrials.gov/study/NCT05905367 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | FENTANYL | targetBased | 4 | Recruiting | 29/01/2024 | https://clinicaltrials.gov/study/NCT05905367 | 1 | GoF | protect | |
Measurement of TR-FRET detection format artefact in the screen for agonists of steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | PPARG | Peroxisome proliferator-activated receptor gamma | schizophrenia | ROSIGLITAZONE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00337350 | 1 | GoF | protect | |
Measurement of TR-FRET detection format artefact in the screen for agonists of steroid receptor coactivator 2 (SRC-2) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | PPARG | Peroxisome proliferator-activated receptor gamma | schizophrenia | ROSIGLITAZONE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00337350 | 1 | GoF | protect | |
Measurement of TR-FRET detection format artefact in the screen for agonists of steroid receptor coactivator 3 (SRC-3) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | PPARG | Peroxisome proliferator-activated receptor gamma | schizophrenia | ROSIGLITAZONE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00337350 | 1 | GoF | protect | |
Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | PPARG | Peroxisome proliferator-activated receptor gamma | schizophrenia | ROSIGLITAZONE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00337350 | 1 | GoF | protect | |
Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 2 (SRC-2) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | PPARG | Peroxisome proliferator-activated receptor gamma | schizophrenia | ROSIGLITAZONE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00337350 | 1 | GoF | protect | |
Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 3 (SRC-3) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | PPARG | Peroxisome proliferator-activated receptor gamma | schizophrenia | ROSIGLITAZONE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00337350 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol-related disorders | NALTREXONE | targetBased | 4 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00145847 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | major depressive disorder | NALTREXONE | targetBased | 4 | Completed | 01/07/2017 | https://clinicaltrials.gov/study/NCT04322526 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | major depressive disorder | NALTREXONE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | cocaine dependence | NALTREXONE | targetBased | 3 | Completed | 01/01/1998 | https://clinicaltrials.gov/study/NCT00167232 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | cocaine dependence | NALTREXONE | targetBased | 3 | Completed | 01/04/1998 | https://clinicaltrials.gov/study/NCT00218660 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | Euphoria | NALTREXONE | targetBased | 4 | Completed | 01/09/2012 | https://clinicaltrials.gov/study/NCT01673594 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | methamphetamine dependence | NALTREXONE | targetBased | 3 | Not yet recruiting | 01/05/2024 | https://clinicaltrials.gov/study/NCT06233799 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | methamphetamine dependence | NALTREXONE | targetBased | 3 | Not yet recruiting | 01/05/2024 | https://clinicaltrials.gov/study/NCT06233799 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | methamphetamine dependence | NALTREXONE | targetBased | 3 | Completed | 05/05/2017 | https://clinicaltrials.gov/study/NCT03078075 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | methamphetamine dependence | NALTREXONE | targetBased | 3 | Completed | 05/05/2017 | https://clinicaltrials.gov/study/NCT03078075 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Withdrawn | 01/11/2009 | https://clinicaltrials.gov/study/NCT01015066 | 1 | LoF | protect | Study personnel left institution, anticipated funding did not occur |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 21/09/2017 | https://clinicaltrials.gov/study/NCT02978417 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT02324725 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01453374 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 3 | Completed | 01/05/2010 | https://clinicaltrials.gov/study/NCT01180647 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 01/01/2013 | https://clinicaltrials.gov/study/NCT01471145 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 3 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01717963 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 3 | Terminated | 01/08/2004 | https://clinicaltrials.gov/study/NCT00156936 | 0.7 | LoF | protect | Business decision |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | sleep apnea | NALTREXONE | targetBased | 4 | Completed | 08/08/2021 | https://clinicaltrials.gov/study/NCT05037032 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Self-injurious behavior | NALTREXONE | targetBased | 3 | Unknown status | 01/07/1997 | https://clinicaltrials.gov/study/NCT00065936 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Self-injurious behavior | NALTREXONE | targetBased | 3 | Unknown status | 01/07/1997 | https://clinicaltrials.gov/study/NCT00065936 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Self-injurious behavior | NALTREXONE | targetBased | 4 | Withdrawn | 22/02/2014 | https://clinicaltrials.gov/study/NCT02726035 | 1 | LoF | protect | PI deceased |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Self-injurious behavior | NALTREXONE | targetBased | 4 | Withdrawn | 22/02/2014 | https://clinicaltrials.gov/study/NCT02726035 | 1 | LoF | protect | PI deceased |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | eating disorder | NALTREXONE | targetBased | 4 | Completed | 01/10/1995 | https://clinicaltrials.gov/study/NCT00000448 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | eating disorder | NALTREXONE | targetBased | 4 | Completed | 01/10/1995 | https://clinicaltrials.gov/study/NCT00000448 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | eating disorder | NALTREXONE | targetBased | 4 | Completed | 01/10/1995 | https://clinicaltrials.gov/study/NCT00000448 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | methamphetamine dependence | NALTREXONE | targetBased | 3 | Completed | 05/05/2017 | https://clinicaltrials.gov/study/NCT03078075 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | methamphetamine dependence | NALTREXONE | targetBased | 3 | Not yet recruiting | 01/05/2024 | https://clinicaltrials.gov/study/NCT06233799 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 3 | Completed | 01/09/2007 | https://clinicaltrials.gov/study/NCT00577408 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 4 | Completed | 01/01/2013 | https://clinicaltrials.gov/study/NCT01471145 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 4 | Completed | 01/01/2013 | https://clinicaltrials.gov/study/NCT01471145 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT02324725 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT02324725 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 4 | Completed | 27/06/2014 | https://clinicaltrials.gov/study/NCT01999946 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 4 | Completed | 27/06/2014 | https://clinicaltrials.gov/study/NCT01999946 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALTREXONE | targetBased | 3 | Completed | 01/05/2010 | https://clinicaltrials.gov/study/NCT01100853 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALTREXONE | targetBased | 3 | Completed | 01/05/2010 | https://clinicaltrials.gov/study/NCT01100853 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALTREXONE | targetBased | 4 | Completed | 01/03/2012 | https://clinicaltrials.gov/study/NCT01563718 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALTREXONE | targetBased | 4 | Completed | 01/03/2012 | https://clinicaltrials.gov/study/NCT01563718 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALTREXONE | targetBased | 4 | Completed | 01/06/2013 | https://clinicaltrials.gov/study/NCT01843023 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALTREXONE | targetBased | 4 | Completed | 01/06/2013 | https://clinicaltrials.gov/study/NCT01843023 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol abuse | NALTREXONE | targetBased | 3 | Unknown status | 01/02/2007 | https://clinicaltrials.gov/study/NCT01115894 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol abuse | NALTREXONE | targetBased | 4 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00145847 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | post-traumatic stress disorder | NALTREXONE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00006489 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | post-traumatic stress disorder | NALTREXONE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00006489 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | post-traumatic stress disorder | NALTREXONE | targetBased | 3 | Completed | 01/10/2001 | https://clinicaltrials.gov/study/NCT00338962 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | post-traumatic stress disorder | NALTREXONE | targetBased | 3 | Completed | 01/10/2001 | https://clinicaltrials.gov/study/NCT00338962 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | gambling behaviour | NALTREXONE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01528007 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | gambling behaviour | NALTREXONE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01528007 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | gambling behaviour | NALTREXONE | targetBased | 3 | Completed | 01/12/2002 | https://clinicaltrials.gov/study/NCT00053677 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | gambling behaviour | NALTREXONE | targetBased | 3 | Completed | 01/12/2002 | https://clinicaltrials.gov/study/NCT00053677 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | post-traumatic stress disorder | NALTREXONE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00006489 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | post-traumatic stress disorder | NALTREXONE | targetBased | 3 | Completed | 01/10/2001 | https://clinicaltrials.gov/study/NCT00338962 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 4 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT02032433 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 3 | Completed | 01/08/2017 | https://clinicaltrials.gov/study/NCT03232346 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 3 | Completed | 01/06/2014 | https://clinicaltrials.gov/study/NCT01908062 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 3 | Completed | 01/04/2016 | https://clinicaltrials.gov/study/NCT02696434 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 4 | Completed | 01/08/2018 | https://clinicaltrials.gov/study/NCT03647774 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | NALTREXONE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | NALTREXONE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | NALTREXONE | targetBased | 4 | Completed | 01/07/2017 | https://clinicaltrials.gov/study/NCT04322526 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | NALTREXONE | targetBased | 4 | Completed | 01/07/2017 | https://clinicaltrials.gov/study/NCT04322526 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | NALTREXONE | targetBased | 4 | Completed | 01/03/2012 | https://clinicaltrials.gov/study/NCT01563718 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | NALTREXONE | targetBased | 4 | Completed | 01/06/2013 | https://clinicaltrials.gov/study/NCT01843023 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | NALTREXONE | targetBased | 3 | Completed | 01/05/2010 | https://clinicaltrials.gov/study/NCT01100853 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | Self-injurious behavior | NALTREXONE | targetBased | 3 | Unknown status | 01/07/1997 | https://clinicaltrials.gov/study/NCT00065936 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | Self-injurious behavior | NALTREXONE | targetBased | 4 | Withdrawn | 22/02/2014 | https://clinicaltrials.gov/study/NCT02726035 | 1 | LoF | protect | PI deceased |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 3 | Completed | 01/09/2007 | https://clinicaltrials.gov/study/NCT00577408 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 4 | Completed | 27/06/2014 | https://clinicaltrials.gov/study/NCT01999946 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 4 | Completed | 01/01/2013 | https://clinicaltrials.gov/study/NCT01471145 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | NALTREXONE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT02324725 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | depressive disorder | NALTREXONE | targetBased | 4 | Completed | 01/01/2018 | https://clinicaltrials.gov/study/NCT03386448 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | depressive disorder | NALTREXONE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | depressive disorder | NALTREXONE | targetBased | 3 | Completed | 01/10/2001 | https://clinicaltrials.gov/study/NCT00338962 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | nicotine dependence | NALTREXONE | targetBased | 4 | Completed | 26/09/1997 | https://clinicaltrials.gov/study/NCT00000437 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | nicotine dependence | NALTREXONE | targetBased | 4 | Completed | 26/09/1997 | https://clinicaltrials.gov/study/NCT00000437 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | nicotine dependence | NALTREXONE | targetBased | 3 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00218153 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | nicotine dependence | NALTREXONE | targetBased | 3 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00218153 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | nicotine dependence | NALTREXONE | targetBased | 4 | Completed | 01/09/1998 | https://clinicaltrials.gov/study/NCT00000447 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | nicotine dependence | NALTREXONE | targetBased | 4 | Completed | 01/09/1998 | https://clinicaltrials.gov/study/NCT00000447 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | gambling behaviour | NALTREXONE | targetBased | 3 | Completed | 01/12/2002 | https://clinicaltrials.gov/study/NCT00053677 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | gambling behaviour | NALTREXONE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01528007 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | attention deficit hyperactivity disorder | NALTREXONE | targetBased | 4 | Terminated | 01/11/2012 | https://clinicaltrials.gov/study/NCT01721330 | 1 | LoF | protect | Competing studies |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | attention deficit hyperactivity disorder | NALTREXONE | targetBased | 4 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT01873729 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | attention deficit hyperactivity disorder | NALTREXONE | targetBased | 4 | Completed | 01/10/2013 | https://clinicaltrials.gov/study/NCT01993108 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 01/01/2013 | https://clinicaltrials.gov/study/NCT01471145 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT02324725 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT02324725 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01453374 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01453374 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 21/09/2017 | https://clinicaltrials.gov/study/NCT02978417 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALTREXONE | targetBased | 4 | Completed | 21/09/2017 | https://clinicaltrials.gov/study/NCT02978417 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol-related disorders | NALTREXONE | targetBased | 4 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00145847 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol-related disorders | NALTREXONE | targetBased | 4 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00145847 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol abuse | NALTREXONE | targetBased | 4 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00145847 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol abuse | NALTREXONE | targetBased | 4 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00145847 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol abuse | NALTREXONE | targetBased | 3 | Unknown status | 01/02/2007 | https://clinicaltrials.gov/study/NCT01115894 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol abuse | NALTREXONE | targetBased | 3 | Unknown status | 01/02/2007 | https://clinicaltrials.gov/study/NCT01115894 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | Borderline personality disorder | NALTREXONE | targetBased | 3 | Terminated | 01/10/2005 | https://clinicaltrials.gov/study/NCT00124839 | 0.7 | LoF | protect | Difficulties in recruiting enough subjects |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | NALTREXONE | targetBased | 3 | Completed | 01/10/2001 | https://clinicaltrials.gov/study/NCT00338962 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | NALTREXONE | targetBased | 3 | Completed | 01/10/2001 | https://clinicaltrials.gov/study/NCT00338962 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | NALTREXONE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | NALTREXONE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | NALTREXONE | targetBased | 4 | Completed | 01/01/2018 | https://clinicaltrials.gov/study/NCT03386448 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | NALTREXONE | targetBased | 4 | Completed | 01/01/2018 | https://clinicaltrials.gov/study/NCT03386448 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Unknown status | 01/03/2003 | https://clinicaltrials.gov/study/NCT00120601 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00000445 | 1 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00000445 | 1 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Terminated | 01/08/2012 | https://clinicaltrials.gov/study/NCT01638377 | 1 | LoF | protect | Recruitment proved to be extremely difficult. |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Terminated | 01/08/2012 | https://clinicaltrials.gov/study/NCT01638377 | 1 | LoF | protect | Recruitment proved to be extremely difficult. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00453804 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00453804 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Borderline personality disorder | NALTREXONE | targetBased | 3 | Terminated | 01/10/2005 | https://clinicaltrials.gov/study/NCT00124839 | 0.7 | LoF | protect | Difficulties in recruiting enough subjects |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Borderline personality disorder | NALTREXONE | targetBased | 3 | Terminated | 01/10/2005 | https://clinicaltrials.gov/study/NCT00124839 | 0.7 | LoF | protect | Difficulties in recruiting enough subjects |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Completed | 01/06/2009 | https://clinicaltrials.gov/study/NCT00920829 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00000449 | 1 | LoF | protect | ||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Withdrawn | 01/03/2022 | https://clinicaltrials.gov/study/NCT05087771 | 1 | LoF | protect | no longer randomized, drug being offered to all patients |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00006489 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cd11c435-b0f0-4bb9-ae78-60f101f3703f | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00000455 | 1 | LoF | protect | ||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALTREXONE | targetBased | 4 | Completed | 01/09/2000 | https://clinicaltrials.gov/study/NCT00006449 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 4 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT02032433 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 4 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT02032433 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 3 | Completed | 01/08/2017 | https://clinicaltrials.gov/study/NCT03232346 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 3 | Completed | 01/08/2017 | https://clinicaltrials.gov/study/NCT03232346 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 3 | Completed | 01/04/2016 | https://clinicaltrials.gov/study/NCT02696434 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 3 | Completed | 01/04/2016 | https://clinicaltrials.gov/study/NCT02696434 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 4 | Completed | 01/08/2018 | https://clinicaltrials.gov/study/NCT03647774 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | NALTREXONE | targetBased | 4 | Completed | 01/08/2018 | https://clinicaltrials.gov/study/NCT03647774 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | attention deficit hyperactivity disorder | NALTREXONE | targetBased | 4 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT01873729 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | attention deficit hyperactivity disorder | NALTREXONE | targetBased | 4 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT01873729 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | attention deficit hyperactivity disorder | NALTREXONE | targetBased | 4 | Terminated | 01/11/2012 | https://clinicaltrials.gov/study/NCT01721330 | 1 | LoF | protect | Competing studies |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | attention deficit hyperactivity disorder | NALTREXONE | targetBased | 4 | Terminated | 01/11/2012 | https://clinicaltrials.gov/study/NCT01721330 | 1 | LoF | protect | Competing studies |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | attention deficit hyperactivity disorder | NALTREXONE | targetBased | 4 | Completed | 01/10/2013 | https://clinicaltrials.gov/study/NCT01993108 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | attention deficit hyperactivity disorder | NALTREXONE | targetBased | 4 | Completed | 01/10/2013 | https://clinicaltrials.gov/study/NCT01993108 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | NALTREXONE | targetBased | 3 | Completed | 01/01/1998 | https://clinicaltrials.gov/study/NCT00167232 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | NALTREXONE | targetBased | 3 | Completed | 01/01/1998 | https://clinicaltrials.gov/study/NCT00167232 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | NALTREXONE | targetBased | 3 | Completed | 01/04/1998 | https://clinicaltrials.gov/study/NCT00218660 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | NALTREXONE | targetBased | 3 | Completed | 01/04/1998 | https://clinicaltrials.gov/study/NCT00218660 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | nicotine dependence | NALTREXONE | targetBased | 3 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00218153 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | nicotine dependence | NALTREXONE | targetBased | 4 | Completed | 01/09/1998 | https://clinicaltrials.gov/study/NCT00000447 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | nicotine dependence | NALTREXONE | targetBased | 4 | Completed | 26/09/1997 | https://clinicaltrials.gov/study/NCT00000437 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | sleep apnea | NALTREXONE | targetBased | 4 | Completed | 08/08/2021 | https://clinicaltrials.gov/study/NCT05037032 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | sleep apnea | NALTREXONE | targetBased | 4 | Completed | 08/08/2021 | https://clinicaltrials.gov/study/NCT05037032 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Euphoria | NALTREXONE | targetBased | 4 | Completed | 01/09/2012 | https://clinicaltrials.gov/study/NCT01673594 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Euphoria | NALTREXONE | targetBased | 4 | Completed | 01/09/2012 | https://clinicaltrials.gov/study/NCT01673594 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MEPERIDINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fae5cc34-5917-4445-9516-25f97ffca8db | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MEPERIDINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fae5cc34-5917-4445-9516-25f97ffca8db | 1 | GoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | DEXTROAMPHETAMINE | targetBased | 4 | Terminated | 01/09/2001 | https://clinicaltrials.gov/study/NCT00296686 | 1 | protect | Study is no longer funded. | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | DEXTROAMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d6394df5-f2c9-47eb-b57e-f3e9cfd94f84 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | DEXTROAMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | drug dependence | DEXTROAMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=35744538-1704-4ee0-954d-52710cf3456d | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE | targetBased | 4 | Completed | 05/08/2003 | https://clinicaltrials.gov/study/NCT00506727 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE | targetBased | 4 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00468143 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=141a7970-3f06-44ea-9ab7-aeece2c085fc | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06BA02 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d6394df5-f2c9-47eb-b57e-f3e9cfd94f84 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT01220440 | 1 | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Sleep Disorder | TRAZODONE | targetBased | 3 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT01468038 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | TRAZODONE | targetBased | 4 | Not yet recruiting | 01/03/2025 | https://clinicaltrials.gov/study/NCT05085808 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE | targetBased | 3 | Completed | 01/12/2012 | https://clinicaltrials.gov/study/NCT02086929 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE | targetBased | 4 | Unknown status | 01/06/2012 | https://clinicaltrials.gov/study/NCT01764867 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17b3356e-458d-47f6-89a5-80828ab48d4c | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE | targetBased | 3 | Completed | 01/06/2007 | https://clinicaltrials.gov/study/NCT00775203 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=10a30879-f6e2-4030-95b8-0979c18c418a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=66da652a-72b4-c17f-e053-2a91aa0a8d69 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | TRAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=49196e9e-aeef-4663-8be9-6b523ae7fb7a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | TRAZODONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX05 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | TRAZODONE | targetBased | 4 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00659919 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | TRAZODONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | TRAZODONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | TRAZODONE | targetBased | 4 | Active, not recruiting | 25/02/2022 | https://clinicaltrials.gov/study/NCT04468776 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | TRAZODONE | targetBased | 4 | Active, not recruiting | 01/06/2011 | https://clinicaltrials.gov/study/NCT01651442 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | TRAZODONE | targetBased | 3 | Recruiting | 25/02/2021 | https://clinicaltrials.gov/study/NCT03668041 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | TRAZODONE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | TRAZODONE | targetBased | 3 | Withdrawn | 01/12/2019 | https://clinicaltrials.gov/study/NCT03852160 | 0.7 | LoF | protect | New design was developed to better fit company strategy, a new study has replaced 5413541TRD3011 study |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | TRAZODONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | TRAZODONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | NEFAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0bd4c34a-4f43-4c84-8b98-1d074cba97d5 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | NEFAZODONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX06 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | NEFAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0bd4c34a-4f43-4c84-8b98-1d074cba97d5 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | cocaine dependence | NEFAZODONE | targetBased | 3 | Completed | 01/01/1999 | https://clinicaltrials.gov/study/NCT00000293 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | NEFAZODONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00231348 | 1 | LoF | protect | ||
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_agonists | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 16/12/2020 | https://clinicaltrials.gov/study/NCT04659161 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_PAMs | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 01/02/2021 | https://clinicaltrials.gov/study/NCT04659174 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_antgonists | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 01/02/2021 | https://clinicaltrials.gov/study/NCT04659174 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_agonists | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 01/02/2021 | https://clinicaltrials.gov/study/NCT04659174 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_PAMs | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Terminated | 08/11/2022 | https://clinicaltrials.gov/study/NCT05643170 | 0.7 | GoF | protect | Company's business decision. |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_antgonists | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Terminated | 08/11/2022 | https://clinicaltrials.gov/study/NCT05643170 | 0.7 | GoF | protect | Company's business decision. |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_agonists | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Terminated | 08/11/2022 | https://clinicaltrials.gov/study/NCT05643170 | 0.7 | GoF | protect | Company's business decision. |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_PAMs | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Active, not recruiting | 02/06/2021 | https://clinicaltrials.gov/study/NCT04820309 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_antgonists | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Active, not recruiting | 02/06/2021 | https://clinicaltrials.gov/study/NCT04820309 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_agonists | CHRM4 | Muscarinic acetylcholine receptor M4 | schizophrenia | XANOMELINE | targetBased | 3 | Active, not recruiting | 02/06/2021 | https://clinicaltrials.gov/study/NCT04820309 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 16/12/2020 | https://clinicaltrials.gov/study/NCT04659161 | 0.7 | GoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 16/12/2020 | https://clinicaltrials.gov/study/NCT04659161 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 16/12/2020 | https://clinicaltrials.gov/study/NCT04659161 | 0.7 | GoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 16/12/2020 | https://clinicaltrials.gov/study/NCT04659161 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 16/12/2020 | https://clinicaltrials.gov/study/NCT04659161 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 06/04/2021 | https://clinicaltrials.gov/study/NCT04738123 | 0.7 | GoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 06/04/2021 | https://clinicaltrials.gov/study/NCT04738123 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 06/04/2021 | https://clinicaltrials.gov/study/NCT04738123 | 0.7 | GoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 06/04/2021 | https://clinicaltrials.gov/study/NCT04738123 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | XANOMELINE | targetBased | 3 | Completed | 06/04/2021 | https://clinicaltrials.gov/study/NCT04738123 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | ALFENTANIL | targetBased | 4 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT02022488 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | ALFENTANIL | targetBased | 4 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT02022488 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | TRIMIPRAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA06 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | TRIMIPRAMINE | targetBased | 4 | Unknown status | 01/09/2011 | https://clinicaltrials.gov/study/NCT02237937 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | TRIMIPRAMINE | targetBased | 4 | Unknown status | 01/09/2011 | https://clinicaltrials.gov/study/NCT02237937 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | TRIMIPRAMINE | targetBased | 4 | Unknown status | 01/09/2011 | https://clinicaltrials.gov/study/NCT02237937 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | TRIMIPRAMINE | targetBased | 4 | Unknown status | 01/09/2011 | https://clinicaltrials.gov/study/NCT02237937 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | TRIMIPRAMINE | targetBased | 4 | Unknown status | 01/09/2011 | https://clinicaltrials.gov/study/NCT02237937 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | TRIMIPRAMINE | targetBased | 4 | Unknown status | 01/09/2011 | https://clinicaltrials.gov/study/NCT02237937 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | TRIMIPRAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA06 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | TRIMIPRAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | TRIMIPRAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA06 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | TRIMIPRAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | TRIMIPRAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA06 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | TRIMIPRAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | TRIMIPRAMINE | targetBased | 4 | Unknown status | 01/09/2011 | https://clinicaltrials.gov/study/NCT02237937 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIMIPRAMINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | METHADONE | targetBased | 3 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00378079 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | METHADONE | targetBased | 3 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00378079 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | METHADONE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00310934 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | METHADONE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00310934 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BC02 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BC02 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4a44bde6-c348-4316-b0e0-c24b407cb823 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4a44bde6-c348-4316-b0e0-c24b407cb823 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c796a39-d87f-4358-9d4b-26e27464b642 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c796a39-d87f-4358-9d4b-26e27464b642 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE | targetBased | 4 | Completed | 01/04/2009 | https://clinicaltrials.gov/study/NCT00879996 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE | targetBased | 4 | Unknown status | 01/06/2009 | https://clinicaltrials.gov/study/NCT01047956 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE | targetBased | 4 | Unknown status | 01/06/2009 | https://clinicaltrials.gov/study/NCT01047956 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06cc3fba-68f9-4188-a239-fbd37a9f563a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06cc3fba-68f9-4188-a239-fbd37a9f563a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c796a39-d87f-4358-9d4b-26e27464b642 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c796a39-d87f-4358-9d4b-26e27464b642 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | METHADONE | targetBased | 4 | Completed | 01/10/2016 | https://clinicaltrials.gov/study/NCT02851303 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | METHADONE | targetBased | 4 | Completed | 01/10/2016 | https://clinicaltrials.gov/study/NCT02851303 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | METHADONE | targetBased | 4 | Completed | 01/01/2007 | https://clinicaltrials.gov/study/NCT01723722 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | METHADONE | targetBased | 4 | Completed | 01/01/2007 | https://clinicaltrials.gov/study/NCT01723722 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | METHADONE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01804075 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | METHADONE | targetBased | 4 | Completed | 01/01/2011 | https://clinicaltrials.gov/study/NCT01804075 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | METHADONE | targetBased | 4 | Completed | 02/10/2017 | https://clinicaltrials.gov/study/NCT03033732 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | METHADONE | targetBased | 4 | Completed | 02/10/2017 | https://clinicaltrials.gov/study/NCT03033732 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | METHADONE | targetBased | 4 | Recruiting | 04/06/2024 | https://clinicaltrials.gov/study/NCT06323824 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | METHADONE | targetBased | 4 | Recruiting | 04/06/2024 | https://clinicaltrials.gov/study/NCT06323824 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | METHADONE | targetBased | 4 | Recruiting | 29/01/2024 | https://clinicaltrials.gov/study/NCT05905367 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | METHADONE | targetBased | 4 | Recruiting | 29/01/2024 | https://clinicaltrials.gov/study/NCT05905367 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | METHADONE | targetBased | 3 | Completed | 01/02/1995 | https://clinicaltrials.gov/study/NCT00000311 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | METHADONE | targetBased | 3 | Completed | 01/02/1995 | https://clinicaltrials.gov/study/NCT00000311 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=40c95daa-bbd5-48d9-97e4-c87f2c1f0fa5 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | MIRTAZAPINE | targetBased | 4 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT02191124 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | MIRTAZAPINE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01601002 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | MIRTAZAPINE | targetBased | 4 | Unknown status | 01/05/2015 | https://clinicaltrials.gov/study/NCT02711215 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8feda54f-a3fa-4108-bfc4-c15b0eab4396 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | MIRTAZAPINE | targetBased | 4 | Unknown status | 01/06/2012 | https://clinicaltrials.gov/study/NCT01764867 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | MIRTAZAPINE | targetBased | 4 | Terminated | 01/05/2009 | https://clinicaltrials.gov/study/NCT00926835 | 1 | LoF | protect | due to patient recruitment difficulties |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | MIRTAZAPINE | targetBased | 4 | Completed | 01/10/2006 | https://clinicaltrials.gov/study/NCT00449189 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | MIRTAZAPINE | targetBased | 4 | Completed | 01/07/2010 | https://clinicaltrials.gov/study/NCT01178671 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5990a1f2-a5c9-4f40-ab5f-a32c1bd218b9 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b8df747e-dfce-4411-b892-086532ffabfb | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a4c012f0-50b6-42fb-9f06-a14632f23f2e | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=34c0b734-98ca-4aec-965f-e55edd3317f3 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=18fbbcbb-73bd-4d22-8f4e-9a2777f0daf8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=de019322-8145-4aba-95e1-d238df4df475 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=711aa80b-8fc6-49e6-9494-3db31d9b53a4 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | MIRTAZAPINE | targetBased | 4 | Completed | 01/11/2010 | https://clinicaltrials.gov/study/NCT01263080 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | MIRTAZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive episode | MIRTAZAPINE | targetBased | 4 | Completed | 01/12/2010 | https://clinicaltrials.gov/study/NCT01109693 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | MIRTAZAPINE | targetBased | 3 | Completed | 01/01/2017 | https://clinicaltrials.gov/study/NCT03031184 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | MIRTAZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | MIRTAZAPINE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00177567 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism spectrum disorder | MIRTAZAPINE | targetBased | 3 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01302964 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | heroin dependence | MIRTAZAPINE | targetBased | 3 | Unknown status | 01/05/2013 | https://clinicaltrials.gov/study/NCT02541526 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | MIRTAZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8feda54f-a3fa-4108-bfc4-c15b0eab4396 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | MIRTAZAPINE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00021528 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | MIRTAZAPINE | targetBased | 4 | Not yet recruiting | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148522 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | MIRTAZAPINE | targetBased | 4 | Completed | 14/11/2012 | https://clinicaltrials.gov/study/NCT01458626 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | MIRTAZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | MIRTAZAPINE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | MIRTAZAPINE | targetBased | 4 | Unknown status | 01/08/2017 | https://clinicaltrials.gov/study/NCT03219008 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | MIRTAZAPINE | targetBased | 4 | Terminated | 01/08/2011 | https://clinicaltrials.gov/study/NCT01465919 | 1 | LoF | protect | Due to the recent change in standard of care for hepatitis C. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | MIRTAZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | MIRTAZAPINE | targetBased | 4 | Completed | 15/06/2021 | https://clinicaltrials.gov/study/NCT04908605 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | REMOXIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL04 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | REMOXIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | REMOXIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL04 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | REMOXIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | REMOXIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL04 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | REMOXIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL04 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | OXYCODONE | targetBased | 4 | Not yet recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT06444997 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | OXYCODONE | targetBased | 4 | Not yet recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT06444997 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8a9529a3-8922-6b50-e053-2995a90a4b08 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3848642e-cc9e-4150-8199-281b294c18bc | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3848642e-cc9e-4150-8199-281b294c18bc | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=504aa63a-4772-2e03-e054-00144ff88e88 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=504aa63a-4772-2e03-e054-00144ff88e88 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02101840 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02101840 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | OXYCODONE | targetBased | 4 | Completed | 01/08/2019 | https://clinicaltrials.gov/study/NCT04015908 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | OXYCODONE | targetBased | 4 | Terminated | 14/09/2016 | https://clinicaltrials.gov/study/NCT02741076 | 1 | GoF | protect | Inability to recruit sufficient no. of subjects over an acceptable time period |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | OXYCODONE | targetBased | 4 | Terminated | 14/09/2016 | https://clinicaltrials.gov/study/NCT02741076 | 1 | GoF | protect | Inability to recruit sufficient no. of subjects over an acceptable time period |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | OXYCODONE | targetBased | 4 | Completed | 01/07/2011 | https://clinicaltrials.gov/study/NCT01374763 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | OXYCODONE | targetBased | 4 | Completed | 01/07/2011 | https://clinicaltrials.gov/study/NCT01374763 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | OXYCODONE | targetBased | 4 | Completed | 20/05/2020 | https://clinicaltrials.gov/study/NCT04396587 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | OXYCODONE | targetBased | 4 | Completed | 20/05/2020 | https://clinicaltrials.gov/study/NCT04396587 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | sleep apnea | OXYCODONE | targetBased | 4 | Completed | 01/03/2018 | https://clinicaltrials.gov/study/NCT03454217 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | sleep apnea | OXYCODONE | targetBased | 4 | Completed | 01/03/2018 | https://clinicaltrials.gov/study/NCT03454217 | 1 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | postpartum depression | ESTRADIOL | targetBased | 4 | Terminated | 01/08/2008 | https://clinicaltrials.gov/study/NCT00744328 | 1 | GoF | protect | Recruitment Issues |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | postpartum depression | ESTRADIOL | targetBased | 4 | Terminated | 01/08/2008 | https://clinicaltrials.gov/study/NCT00744328 | 1 | GoF | protect | Recruitment Issues |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | dysphoria | ESTRADIOL | targetBased | 4 | Unknown status | 06/02/2017 | https://clinicaltrials.gov/study/NCT02715232 | 1 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | dysphoria | ESTRADIOL | targetBased | 4 | Unknown status | 06/02/2017 | https://clinicaltrials.gov/study/NCT02715232 | 1 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | dysphoria | ESTRADIOL | targetBased | 4 | Terminated | 29/12/2022 | https://clinicaltrials.gov/study/NCT05428215 | 1 | GoF | protect | Inability to adequately recruit participants, need for additional study participants based on preliminary data collection |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | dysphoria | ESTRADIOL | targetBased | 4 | Terminated | 29/12/2022 | https://clinicaltrials.gov/study/NCT05428215 | 1 | GoF | protect | Inability to adequately recruit participants, need for additional study participants based on preliminary data collection |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | post-traumatic stress disorder | ESTRADIOL | targetBased | 3 | Recruiting | 24/06/2020 | https://clinicaltrials.gov/study/NCT04192266 | 0.7 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | post-traumatic stress disorder | ESTRADIOL | targetBased | 3 | Recruiting | 24/06/2020 | https://clinicaltrials.gov/study/NCT04192266 | 0.7 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | post-traumatic stress disorder | ESTRADIOL | targetBased | 4 | Recruiting | 29/11/2017 | https://clinicaltrials.gov/study/NCT03371654 | 1 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | post-traumatic stress disorder | ESTRADIOL | targetBased | 4 | Recruiting | 29/11/2017 | https://clinicaltrials.gov/study/NCT03371654 | 1 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | depressive disorder | ESTRADIOL | targetBased | 4 | Completed | 01/10/2015 | https://clinicaltrials.gov/study/NCT02255175 | 1 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | depressive disorder | ESTRADIOL | targetBased | 4 | Completed | 01/10/2015 | https://clinicaltrials.gov/study/NCT02255175 | 1 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | depressive disorder | ESTRADIOL | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00030147 | 1 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | depressive disorder | ESTRADIOL | targetBased | 4 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00030147 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | SUFENTANIL | targetBased | 4 | Not yet recruiting | 15/11/2022 | https://clinicaltrials.gov/study/NCT05624424 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | SUFENTANIL | targetBased | 4 | Not yet recruiting | 15/11/2022 | https://clinicaltrials.gov/study/NCT05624424 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | SUFENTANIL | targetBased | 4 | Completed | 20/05/2020 | https://clinicaltrials.gov/study/NCT04396587 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | SUFENTANIL | targetBased | 4 | Completed | 20/05/2020 | https://clinicaltrials.gov/study/NCT04396587 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | postpartum depression | SUFENTANIL | targetBased | 4 | Recruiting | 01/05/2023 | https://clinicaltrials.gov/study/NCT05826327 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | postpartum depression | SUFENTANIL | targetBased | 4 | Recruiting | 01/05/2023 | https://clinicaltrials.gov/study/NCT05826327 | 1 | GoF | protect | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | drug dependence | AMANTADINE | targetBased | 4 | Completed | 01/03/1997 | https://clinicaltrials.gov/study/NCT00015236 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | AMANTADINE | targetBased | 4 | Withdrawn | 01/09/2005 | https://clinicaltrials.gov/study/NCT00127114 | 1 | LoF | protect | No funding and exclusion criteria were to stringent. | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | AMANTADINE | targetBased | 3 | Unknown status | 01/05/2010 | https://clinicaltrials.gov/study/NCT00999505 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | AMANTADINE | targetBased | 3 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00401973 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | treatment resistant depression | AMANTADINE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizoaffective disorder | AMANTADINE | targetBased | 3 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00401973 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | cocaine dependence | AMANTADINE | targetBased | 4 | Completed | 01/03/1997 | https://clinicaltrials.gov/study/NCT00015236 | 1 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | CYCLOBENZAPRINE | targetBased | 3 | Terminated | 27/03/2017 | https://clinicaltrials.gov/study/NCT03062540 | 0.35 | LoF | protect | Stopped early due to inadequate separation on primary efficacy endpoint at Week 12 according to Interim Analysis conducted on the first 274 (50%) patients. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | CYCLOBENZAPRINE | targetBased | 3 | Completed | 19/04/2018 | https://clinicaltrials.gov/study/NCT03508700 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | CYCLOBENZAPRINE | targetBased | 3 | Terminated | 07/03/2019 | https://clinicaltrials.gov/study/NCT03841773 | 0.7 | LoF | protect | Interim Analysis results |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | CYCLOBENZAPRINE | targetBased | 3 | Terminated | 20/06/2017 | https://clinicaltrials.gov/study/NCT03110575 | 0.35 | LoF | protect | Stopped early due to inadequate separation on primary efficacy endpoint in the lead-in HONOR study, TNX-CY-P301 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | postpartum depression | ETHINYL ESTRADIOL | targetBased | 4 | Unknown status | 01/07/2014 | https://clinicaltrials.gov/study/NCT02210702 | 1 | GoF | protect | |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | postpartum depression | ETHINYL ESTRADIOL | targetBased | 4 | Unknown status | 01/07/2014 | https://clinicaltrials.gov/study/NCT02210702 | 1 | GoF | protect | |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | unipolar depression | MINAPRINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX07 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE | targetBased | 4 | Unknown status | 01/02/2014 | https://clinicaltrials.gov/study/NCT02040883 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE | targetBased | 4 | Unknown status | 01/10/2016 | https://clinicaltrials.gov/study/NCT02935998 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE | targetBased | 4 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00199940 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00148564 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00634348 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE | targetBased | 4 | Not yet recruiting | 01/05/2021 | https://clinicaltrials.gov/study/NCT04446234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00515723 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b4001db4-1ccb-42f3-af4a-7276c51f4ad5 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE | targetBased | 4 | Unknown status | 01/09/2013 | https://clinicaltrials.gov/study/NCT01893229 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE | targetBased | 4 | Unknown status | 01/09/2013 | https://clinicaltrials.gov/study/NCT01893229 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE | targetBased | 4 | Unknown status | 01/09/2013 | https://clinicaltrials.gov/study/NCT01893229 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE | targetBased | 4 | Unknown status | 01/09/2013 | https://clinicaltrials.gov/study/NCT01893229 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE | targetBased | 4 | Unknown status | 01/09/2013 | https://clinicaltrials.gov/study/NCT01893229 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE | targetBased | 4 | Unknown status | 01/09/2013 | https://clinicaltrials.gov/study/NCT01893229 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT02526030 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2010 | https://clinicaltrials.gov/study/NCT01168674 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b4001db4-1ccb-42f3-af4a-7276c51f4ad5 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=315e24c2-2f8c-47d9-b1b1-ce006646098a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00622739 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE | targetBased | 4 | Unknown status | 01/09/2013 | https://clinicaltrials.gov/study/NCT01893229 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=67696348-8039-4bd2-bbae-d4229c92a4d0 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/08/2002 | https://clinicaltrials.gov/study/NCT00048802 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8326928a-2cb6-4f7f-9712-03a425a14c37 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ZIPRASIDONE | targetBased | 4 | Terminated | 01/07/2013 | https://clinicaltrials.gov/study/NCT01844700 | 0.5 | LoF | protect | very slow recruitment, no sufficient results |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ZIPRASIDONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT01157559 | 1 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ZIPRASIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE04 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00406315 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00458211 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00330863 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00515723 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00649064 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ZIPRASIDONE | targetBased | 3 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00657592 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/02/2010 | https://clinicaltrials.gov/study/NCT01168674 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ZIPRASIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AE04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ZIPRASIDONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT01157559 | 1 | LoF | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ZIPRASIDONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT01157559 | 1 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ZIPRASIDONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT01157559 | 1 | LoF | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ZIPRASIDONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT01157559 | 1 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ZIPRASIDONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT01157559 | 1 | LoF | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ZIPRASIDONE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT01157559 | 1 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mood disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00199940 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | ZIPRASIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mood disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00199940 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mood disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00199940 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mood disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00199940 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mood disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00199940 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mood disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00199940 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mood disorder | ZIPRASIDONE | targetBased | 4 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00199940 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00330863 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4890cf77-8da3-46ae-b6f6-abea7aae6b4d | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4890cf77-8da3-46ae-b6f6-abea7aae6b4d | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4890cf77-8da3-46ae-b6f6-abea7aae6b4d | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4890cf77-8da3-46ae-b6f6-abea7aae6b4d | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4890cf77-8da3-46ae-b6f6-abea7aae6b4d | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4890cf77-8da3-46ae-b6f6-abea7aae6b4d | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | OLANZAPINE | targetBased | 4 | Terminated | 01/10/2004 | https://clinicaltrials.gov/study/NCT00767715 | 1 | LoF | protect | Trial discontinued due to low enrollment |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fad5c029-4531-4913-ab7b-0c68a625447f | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fad5c029-4531-4913-ab7b-0c68a625447f | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fad5c029-4531-4913-ab7b-0c68a625447f | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=40506b0c-1444-4e02-8e80-63f92af8a7b9 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=40506b0c-1444-4e02-8e80-63f92af8a7b9 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=40506b0c-1444-4e02-8e80-63f92af8a7b9 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | eating disorder | OLANZAPINE | targetBased | 3 | Terminated | 01/08/2010 | https://clinicaltrials.gov/study/NCT01184443 | 0.7 | LoF | protect | Poor recruitment |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | eating disorder | OLANZAPINE | targetBased | 3 | Terminated | 01/08/2010 | https://clinicaltrials.gov/study/NCT01184443 | 0.7 | LoF | protect | Poor recruitment |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | eating disorder | OLANZAPINE | targetBased | 3 | Terminated | 01/08/2010 | https://clinicaltrials.gov/study/NCT01184443 | 0.7 | LoF | protect | Poor recruitment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00035321 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00108368 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/06/1997 | https://clinicaltrials.gov/study/NCT00001656 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/06/1997 | https://clinicaltrials.gov/study/NCT00001656 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/06/1997 | https://clinicaltrials.gov/study/NCT00001656 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6b28c424-0b7e-4b75-b090-f116b113554e | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=acd8f466-e5f5-4e15-a4fb-14ab8199cda2 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7881c39e-0624-4c14-a6c3-7a9dc81c198c | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f40ac986-c161-49ae-8650-8ae4c59ce5be | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=66ef201f-85eb-44f0-9ef0-1b618c6e0bff | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a3c9ea17-3793-494a-8b32-44e48f9f4503 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=624d55e0-6cee-4366-9490-3b291c777c78 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00088036 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4ff92ebf-6e0d-458e-a000-ec30df7664d7 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=842b438f-86c7-44f2-a614-06915757a4dd | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a1dfb4e7-4143-4422-b7a7-292e4fd75044 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5f3a9abd-aaca-48b9-8cc9-79bb21179ff5 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | OLANZAPINE | targetBased | 4 | Terminated | 01/07/2012 | https://clinicaltrials.gov/study/NCT01592201 | 1 | LoF | protect | This study was early terminated due to insufficient enrollment required for hypothesis testing. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f6ec3e3e-24c3-4360-b712-ca6017af1347 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | OLANZAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01446328 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=636665be-9d7e-443a-8134-e8cc47e6ba24 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c8c2fb7b-210d-4e44-9c86-bb999deec2fe | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c8c2fb7b-210d-4e44-9c86-bb999deec2fe | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c8c2fb7b-210d-4e44-9c86-bb999deec2fe | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c8c2fb7b-210d-4e44-9c86-bb999deec2fe | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c8c2fb7b-210d-4e44-9c86-bb999deec2fe | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c8c2fb7b-210d-4e44-9c86-bb999deec2fe | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00108368 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/06/1997 | https://clinicaltrials.gov/study/NCT00001656 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00035321 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00035321 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00035321 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00035321 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00035321 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00035321 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00035321 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | major depressive disorder | OLANZAPINE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00056472 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | OLANZAPINE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | OLANZAPINE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | OLANZAPINE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | OLANZAPINE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | OLANZAPINE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | OLANZAPINE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | OLANZAPINE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | eating disorder | OLANZAPINE | targetBased | 3 | Terminated | 01/08/2010 | https://clinicaltrials.gov/study/NCT01184443 | 0.7 | LoF | protect | Poor recruitment |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a3c9ea17-3793-494a-8b32-44e48f9f4503 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=30a963ab-b2ee-4949-8c3c-00d0f308dd61 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=30a963ab-b2ee-4949-8c3c-00d0f308dd61 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=30a963ab-b2ee-4949-8c3c-00d0f308dd61 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=30a963ab-b2ee-4949-8c3c-00d0f308dd61 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=30a963ab-b2ee-4949-8c3c-00d0f308dd61 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=30a963ab-b2ee-4949-8c3c-00d0f308dd61 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | obsessive-compulsive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/1992 | https://clinicaltrials.gov/study/NCT00000373 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00088036 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00088036 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00088036 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f40ac986-c161-49ae-8650-8ae4c59ce5be | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=acd8f466-e5f5-4e15-a4fb-14ab8199cda2 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=acd8f466-e5f5-4e15-a4fb-14ab8199cda2 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=acd8f466-e5f5-4e15-a4fb-14ab8199cda2 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=acd8f466-e5f5-4e15-a4fb-14ab8199cda2 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=acd8f466-e5f5-4e15-a4fb-14ab8199cda2 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=acd8f466-e5f5-4e15-a4fb-14ab8199cda2 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/07/2004 | https://clinicaltrials.gov/study/NCT00090012 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00303602 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00303602 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00303602 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00303602 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00303602 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00303602 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | eating disorder | OLANZAPINE | targetBased | 3 | Terminated | 01/08/2010 | https://clinicaltrials.gov/study/NCT01184443 | 0.7 | LoF | protect | Poor recruitment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | eating disorder | OLANZAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d976599a-0ee0-4fa4-afe6-bdfbca570afe | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=96ddc4f5-43be-5d42-e053-2a95a90a5d12 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e9ac2bd3-dbff-4b1a-952f-da3909c6e4ee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8626e68-088d-47ff-bf06-489a778815aa | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | OLANZAPINE | targetBased | 4 | Completed | 01/12/2006 | https://clinicaltrials.gov/study/NCT00402324 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6b28c424-0b7e-4b75-b090-f116b113554e | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=66ef201f-85eb-44f0-9ef0-1b618c6e0bff | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2f6ceda3-3edc-4427-98a6-23e3c930c44d | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=97ae6a74-8904-4d74-99af-2b679c89f516 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ad42af27-3801-4c29-9e4c-6752cb5f735c | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3c28cf18-01a3-468a-ab3e-8aa82f918251 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80a810aa-d34c-48ca-a9c9-9a79e01afcee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=250ed608-092c-4e19-884f-a15bdea065d7 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=15c99a41-322d-4ac6-b514-bd381be8aa7b | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/06/1997 | https://clinicaltrials.gov/study/NCT00001656 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00108368 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00108368 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00108368 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00108368 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00108368 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00108368 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00337662 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Withdrawn | 01/04/2008 | https://clinicaltrials.gov/study/NCT00672464 | 1 | LoF | protect | lack of funding |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/03/2012 | https://clinicaltrials.gov/study/NCT02137993 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00303602 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/03/2009 | https://clinicaltrials.gov/study/NCT00981526 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00330863 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | OLANZAPINE | targetBased | 4 | Terminated | 01/09/2017 | https://clinicaltrials.gov/study/NCT03246620 | 1 | LoF | protect | The study was terminated prematurely due to difficulties in patient recruitment and associated potential for selection bias. |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=15c99a41-322d-4ac6-b514-bd381be8aa7b | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=15c99a41-322d-4ac6-b514-bd381be8aa7b | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=15c99a41-322d-4ac6-b514-bd381be8aa7b | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7c6ff491-c30c-4ada-85a0-cbee98f2fe32 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7c6ff491-c30c-4ada-85a0-cbee98f2fe32 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7c6ff491-c30c-4ada-85a0-cbee98f2fe32 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c7d0d5fb-2810-410b-b718-27ae019c8169 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16c999a9-399c-4407-883e-8e66b0239ed2 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16c999a9-399c-4407-883e-8e66b0239ed2 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16c999a9-399c-4407-883e-8e66b0239ed2 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fcb7d340-a167-41f2-b85d-916c542067da | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fcb7d340-a167-41f2-b85d-916c542067da | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fcb7d340-a167-41f2-b85d-916c542067da | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00520507 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01427608 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01427608 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01427608 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00520507 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | OLANZAPINE | targetBased | 3 | Withdrawn | 01/06/2005 | https://clinicaltrials.gov/study/NCT00273624 | 0.7 | LoF | protect | Study withdrawn before inclusion of first participant for administrative reasons |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | OLANZAPINE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01427608 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00034801 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | OLANZAPINE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | OLANZAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH03 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e9ac2bd3-dbff-4b1a-952f-da3909c6e4ee | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8626e68-088d-47ff-bf06-489a778815aa | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8626e68-088d-47ff-bf06-489a778815aa | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8626e68-088d-47ff-bf06-489a778815aa | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6b28c424-0b7e-4b75-b090-f116b113554e | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6b28c424-0b7e-4b75-b090-f116b113554e | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6b28c424-0b7e-4b75-b090-f116b113554e | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=15c99a41-322d-4ac6-b514-bd381be8aa7b | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0e986037-41c9-431e-b007-0e7764523fdd | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0e986037-41c9-431e-b007-0e7764523fdd | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0e986037-41c9-431e-b007-0e7764523fdd | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=250ed608-092c-4e19-884f-a15bdea065d7 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=250ed608-092c-4e19-884f-a15bdea065d7 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | unipolar depression | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=250ed608-092c-4e19-884f-a15bdea065d7 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Anorexia | OLANZAPINE | targetBased | 3 | Recruiting | 25/12/2021 | https://clinicaltrials.gov/study/NCT05243251 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | OLANZAPINE | targetBased | 4 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00433121 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | gambling behaviour | OLANZAPINE | targetBased | 3 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00438776 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d976599a-0ee0-4fa4-afe6-bdfbca570afe | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e9ac2bd3-dbff-4b1a-952f-da3909c6e4ee | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e9ac2bd3-dbff-4b1a-952f-da3909c6e4ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e9ac2bd3-dbff-4b1a-952f-da3909c6e4ee | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e9ac2bd3-dbff-4b1a-952f-da3909c6e4ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e9ac2bd3-dbff-4b1a-952f-da3909c6e4ee | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e9ac2bd3-dbff-4b1a-952f-da3909c6e4ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | OLANZAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00746785 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d5051fbc-846b-4946-82df-341fb1216341 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | OLANZAPINE | targetBased | 4 | Terminated | 01/09/2017 | https://clinicaltrials.gov/study/NCT03246620 | 1 | LoF | protect | The study was terminated prematurely due to difficulties in patient recruitment and associated potential for selection bias. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=624d55e0-6cee-4366-9490-3b291c777c78 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=71c6577c-ffea-4934-bc10-2d35942f8a16 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=488fa7d5-9207-4efc-9918-6fc206155e7d | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1e9666ef-4271-4834-8496-ccb3125d83db | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=591f9bb1-f119-4739-87b0-de29c9446727 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aff02cff-d079-bc82-6182-a24c4c6e09a6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a3c9ea17-3793-494a-8b32-44e48f9f4503 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a3c9ea17-3793-494a-8b32-44e48f9f4503 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a3c9ea17-3793-494a-8b32-44e48f9f4503 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a3c9ea17-3793-494a-8b32-44e48f9f4503 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a3c9ea17-3793-494a-8b32-44e48f9f4503 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a3c9ea17-3793-494a-8b32-44e48f9f4503 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety | OLANZAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01687478 | 0.35 | LoF | protect | Interim assessment: Lack of efficacy |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | OLANZAPINE | targetBased | 3 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00958568 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00088036 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00088036 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00088036 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00088036 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | OLANZAPINE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00091650 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00100776 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/06/2009 | https://clinicaltrials.gov/study/NCT00918021 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/06/2009 | https://clinicaltrials.gov/study/NCT00918021 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/06/2009 | https://clinicaltrials.gov/study/NCT00918021 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00246259 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00246259 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | OLANZAPINE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00246259 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | QUETIAPINE | targetBased | 3 | Unknown status | 01/03/2015 | https://clinicaltrials.gov/study/NCT02297763 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | QUETIAPINE | targetBased | 3 | Terminated | 01/06/2009 | https://clinicaltrials.gov/study/NCT00954603 | 0.7 | LoF | protect | few delirious patients were enrolled. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | QUETIAPINE | targetBased | 3 | Terminated | 13/02/2019 | https://clinicaltrials.gov/study/NCT03739476 | 0.7 | LoF | protect | Due to the crisis SARS-COV-2 pandemic: recruitment of patients for the trial is stopped, healthcare pressure generated, suspend the non-essential scheduled surgical activity and on June 30, 2020 medication expired, funding has been exhausted. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | QUETIAPINE | targetBased | 4 | Not yet recruiting | 01/03/2025 | https://clinicaltrials.gov/study/NCT05085808 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | QUETIAPINE | targetBased | 3 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01811459 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329264 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00322595 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT02132286 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/05/2009 | https://clinicaltrials.gov/study/NCT00892463 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE | targetBased | 4 | Terminated | 01/09/2008 | https://clinicaltrials.gov/study/NCT00955474 | 1 | LoF | protect | AstraZeneca halted funding; patent expired for Seroquel (Quetiapine) in 2012 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE | targetBased | 4 | Unknown status | 01/05/2011 | https://clinicaltrials.gov/study/NCT01357967 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT03207438 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00351169 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00292370 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | QUETIAPINE | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00306540 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | QUETIAPINE | targetBased | 4 | Completed | 01/08/2003 | https://clinicaltrials.gov/study/NCT00237393 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=51927f2e-3d56-4644-a6a8-40e0b9a5b579 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2a74e8a0-b2fd-4d7f-8bf8-72148b1d3ae7 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=473a3ac4-67f4-4782-baa9-7f9bdd8761f4 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | QUETIAPINE | targetBased | 3 | Completed | 01/09/2007 | https://clinicaltrials.gov/study/NCT00517387 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | QUETIAPINE | targetBased | 3 | Terminated | 01/06/2009 | https://clinicaltrials.gov/study/NCT00954603 | 0.7 | LoF | protect | few delirious patients were enrolled. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | QUETIAPINE | targetBased | 4 | Not yet recruiting | 01/03/2025 | https://clinicaltrials.gov/study/NCT05085808 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | QUETIAPINE | targetBased | 4 | Not yet recruiting | 01/03/2025 | https://clinicaltrials.gov/study/NCT05085808 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | QUETIAPINE | targetBased | 4 | Not yet recruiting | 01/03/2025 | https://clinicaltrials.gov/study/NCT05085808 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | QUETIAPINE | targetBased | 4 | Not yet recruiting | 01/03/2025 | https://clinicaltrials.gov/study/NCT05085808 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | QUETIAPINE | targetBased | 4 | Not yet recruiting | 01/03/2025 | https://clinicaltrials.gov/study/NCT05085808 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | QUETIAPINE | targetBased | 4 | Not yet recruiting | 01/03/2025 | https://clinicaltrials.gov/study/NCT05085808 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | obsessive-compulsive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/05/2007 | https://clinicaltrials.gov/study/NCT00466609 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | obsessive-compulsive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00564564 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | obsessive-compulsive disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00254735 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00880919 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=577a9332-e340-451f-ac45-350333562fd7 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/05/2007 | https://clinicaltrials.gov/study/NCT00466609 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00564564 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00564564 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00564564 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00564564 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00564564 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00564564 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00156715 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE | targetBased | 4 | Unknown status | 01/10/2009 | https://clinicaltrials.gov/study/NCT00986167 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=daec35ae-a9e7-494a-90a6-c8aff1c65c71 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b007bac6-a207-481c-8aba-03ade1dd6a88 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3ea59594-8a2b-4b64-9aa8-1d53d9027bb0 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aaf50e8a-3c8e-4b19-b539-0384a9b1a707 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aaf50e8a-3c8e-4b19-b539-0384a9b1a707 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aaf50e8a-3c8e-4b19-b539-0384a9b1a707 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aaf50e8a-3c8e-4b19-b539-0384a9b1a707 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aaf50e8a-3c8e-4b19-b539-0384a9b1a707 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aaf50e8a-3c8e-4b19-b539-0384a9b1a707 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar II disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar II disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | drug dependence | QUETIAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00232336 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | drug dependence | QUETIAPINE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00295412 | 1 | LoF | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | drug dependence | QUETIAPINE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00295412 | 1 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | drug dependence | QUETIAPINE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00295412 | 1 | LoF | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | drug dependence | QUETIAPINE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00295412 | 1 | LoF | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | drug dependence | QUETIAPINE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00295412 | 1 | LoF | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | drug dependence | QUETIAPINE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00295412 | 1 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | drug dependence | QUETIAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00232336 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | drug dependence | QUETIAPINE | targetBased | 4 | Completed | https://clinicaltrials.gov/study/NCT00295412 | 1 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT02526030 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | QUETIAPINE | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00254813 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment resistant depression | QUETIAPINE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment resistant depression | QUETIAPINE | targetBased | 3 | Completed | 01/11/2008 | https://clinicaltrials.gov/study/NCT00789854 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT03207438 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT02132286 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT02132286 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT02132286 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT02132286 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT02132286 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT02132286 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00292370 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE | targetBased | 4 | Completed | 01/08/2003 | https://clinicaltrials.gov/study/NCT00237393 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE | targetBased | 4 | Completed | 01/08/2003 | https://clinicaltrials.gov/study/NCT00237393 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE | targetBased | 4 | Completed | 01/08/2003 | https://clinicaltrials.gov/study/NCT00237393 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE | targetBased | 4 | Completed | 01/08/2003 | https://clinicaltrials.gov/study/NCT00237393 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE | targetBased | 4 | Completed | 01/08/2003 | https://clinicaltrials.gov/study/NCT00237393 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE | targetBased | 4 | Completed | 01/08/2003 | https://clinicaltrials.gov/study/NCT00237393 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE | targetBased | 4 | Unknown status | 01/11/2016 | https://clinicaltrials.gov/study/NCT03004521 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE | targetBased | 4 | Unknown status | 01/11/2016 | https://clinicaltrials.gov/study/NCT03004521 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE | targetBased | 4 | Unknown status | 01/11/2016 | https://clinicaltrials.gov/study/NCT03004521 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE | targetBased | 4 | Unknown status | 01/11/2016 | https://clinicaltrials.gov/study/NCT03004521 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE | targetBased | 4 | Unknown status | 01/11/2016 | https://clinicaltrials.gov/study/NCT03004521 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE | targetBased | 4 | Unknown status | 01/11/2016 | https://clinicaltrials.gov/study/NCT03004521 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | alcohol abuse | QUETIAPINE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00156715 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=473a3ac4-67f4-4782-baa9-7f9bdd8761f4 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00113295 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00113295 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00113295 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00113295 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00113295 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00113295 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | cocaine dependence | QUETIAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00232336 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | panic disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2008 | https://clinicaltrials.gov/study/NCT00619892 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE | targetBased | 4 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT02612948 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00515723 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | panic disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2008 | https://clinicaltrials.gov/study/NCT00619892 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | panic disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2008 | https://clinicaltrials.gov/study/NCT00619892 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | panic disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2008 | https://clinicaltrials.gov/study/NCT00619892 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | panic disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2008 | https://clinicaltrials.gov/study/NCT00619892 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | panic disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2008 | https://clinicaltrials.gov/study/NCT00619892 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | panic disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2008 | https://clinicaltrials.gov/study/NCT00619892 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2a74e8a0-b2fd-4d7f-8bf8-72148b1d3ae7 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE | targetBased | 3 | Terminated | 01/04/2009 | https://clinicaltrials.gov/study/NCT00857818 | 0.7 | LoF | protect | Slow Accrual |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE | targetBased | 3 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT00232414 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00107731 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE | targetBased | 4 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01588457 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE | targetBased | 3 | Completed | 01/08/2004 | https://clinicaltrials.gov/study/NCT00227305 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=56eaafad-52a5-4295-85fc-b59d63819ca3 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE | targetBased | 4 | Terminated | 01/06/2010 | https://clinicaltrials.gov/study/NCT01128114 | 1 | LoF | protect | Poor recruitment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6173e1ce-0a85-40b0-99f0-1a6d78e67198 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=904f80af-44b6-d964-1680-ac9e6b61327b | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9737dd88-4700-457d-b596-8f56330232ed | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE | targetBased | 4 | Completed | 01/08/2002 | https://clinicaltrials.gov/study/NCT00048802 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3e482854-45ac-4de9-88a3-e5f70dbdc57b | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00932529 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | QUETIAPINE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance dependence | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance dependence | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance dependence | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance dependence | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance dependence | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance dependence | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00322595 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00322595 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00322595 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00322595 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | QUETIAPINE | targetBased | 4 | Unknown status | 01/05/2010 | https://clinicaltrials.gov/study/NCT01119014 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | QUETIAPINE | targetBased | 3 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00449397 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | QUETIAPINE | targetBased | 4 | Terminated | 01/07/2013 | https://clinicaltrials.gov/study/NCT01844700 | 0.5 | LoF | protect | very slow recruitment, no sufficient results |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | QUETIAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance abuse | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance abuse | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance abuse | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance abuse | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance abuse | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance abuse | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | neurotic disorder | QUETIAPINE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/01/2007 | https://clinicaltrials.gov/study/NCT00423878 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/07/2004 | https://clinicaltrials.gov/study/NCT00090012 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00330863 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 21/05/2018 | https://clinicaltrials.gov/study/NCT03568500 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00246259 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | substance dependence | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00675896 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00253266 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT01200901 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE | targetBased | 4 | Unknown status | 01/11/2016 | https://clinicaltrials.gov/study/NCT03004521 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01133821 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE | targetBased | 4 | Completed | 01/03/2009 | https://clinicaltrials.gov/study/NCT00982345 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE | targetBased | 4 | Unknown status | 01/05/2010 | https://clinicaltrials.gov/study/NCT01119014 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH04 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH04 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH04 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH04 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | QUETIAPINE | targetBased | 3 | Completed | 01/09/2006 | https://clinicaltrials.gov/study/NCT00389064 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | QUETIAPINE | targetBased | 3 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT00314210 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | QUETIAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | QUETIAPINE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | QUETIAPINE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00113295 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | substance abuse | QUETIAPINE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00208143 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2003 | https://clinicaltrials.gov/study/NCT00221468 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | cocaine dependence | QUETIAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00232336 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | cocaine dependence | QUETIAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00232336 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | cocaine dependence | QUETIAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00232336 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | cocaine dependence | QUETIAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00232336 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | cocaine dependence | QUETIAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00232336 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | cocaine dependence | QUETIAPINE | targetBased | 4 | Completed | 01/10/2003 | https://clinicaltrials.gov/study/NCT00232336 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2003 | https://clinicaltrials.gov/study/NCT00221468 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2003 | https://clinicaltrials.gov/study/NCT00221468 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2003 | https://clinicaltrials.gov/study/NCT00221468 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2003 | https://clinicaltrials.gov/study/NCT00221468 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2003 | https://clinicaltrials.gov/study/NCT00221468 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mood disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2003 | https://clinicaltrials.gov/study/NCT00221468 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2a74e8a0-b2fd-4d7f-8bf8-72148b1d3ae7 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol abuse | QUETIAPINE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00156715 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol abuse | QUETIAPINE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00156715 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol abuse | QUETIAPINE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00156715 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol abuse | QUETIAPINE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00156715 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol abuse | QUETIAPINE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00156715 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol abuse | QUETIAPINE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00156715 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | QUETIAPINE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00621647 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | QUETIAPINE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | QUETIAPINE | targetBased | 4 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT02612948 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | QUETIAPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE | targetBased | 4 | Completed | 01/09/2009 | https://clinicaltrials.gov/study/NCT00954122 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE | targetBased | 4 | Completed | 01/12/2006 | https://clinicaltrials.gov/study/NCT00407199 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT01224067 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT01224067 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT01224067 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT01224067 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT01224067 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT01224067 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | QUETIAPINE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | QUETIAPINE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | QUETIAPINE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | QUETIAPINE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | QUETIAPINE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | QUETIAPINE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | QUETIAPINE | targetBased | 3 | Completed | 01/11/2008 | https://clinicaltrials.gov/study/NCT00789854 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00880919 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00880919 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00880919 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00880919 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00880919 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00880919 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | social anxiety disorder | QUETIAPINE | targetBased | 3 | Terminated | 01/06/2006 | https://clinicaltrials.gov/study/NCT00302770 | 0.7 | LoF | protect | This study was terminated due to poor enrollment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | social anxiety disorder | QUETIAPINE | targetBased | 4 | Completed | 01/12/2006 | https://clinicaltrials.gov/study/NCT00407199 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | social anxiety disorder | QUETIAPINE | targetBased | 4 | Completed | 01/03/2006 | https://clinicaltrials.gov/study/NCT01224067 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | social anxiety disorder | QUETIAPINE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00773162 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | BROMPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD06 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | BROMPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | BROMPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD06 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | BROMPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | BROMPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD06 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | BROMPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BROMPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BROMPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | FLUPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | FLUPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | FLUPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB02 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | FLUPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | FLUPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | FLUPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE | targetBased | 3 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00161018 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE | targetBased | 3 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00161018 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE | targetBased | 3 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00161018 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE | targetBased | 3 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00161018 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE | targetBased | 3 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00161018 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE | targetBased | 3 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00161018 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PROCHLORPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB04 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PROCHLORPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PROCHLORPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB04 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PROCHLORPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PROCHLORPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB04 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PROCHLORPERAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB04 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4924c2cf-ffe0-7398-e054-00144ff88e88 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b4aa0-ec8f-4bbc-aa07-58e3da801c3b | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b4aa0-ec8f-4bbc-aa07-58e3da801c3b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b4aa0-ec8f-4bbc-aa07-58e3da801c3b | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b4aa0-ec8f-4bbc-aa07-58e3da801c3b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b4aa0-ec8f-4bbc-aa07-58e3da801c3b | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b4aa0-ec8f-4bbc-aa07-58e3da801c3b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety disorder | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4924c2cf-ffe0-7398-e054-00144ff88e88 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety disorder | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4924c2cf-ffe0-7398-e054-00144ff88e88 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety disorder | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4924c2cf-ffe0-7398-e054-00144ff88e88 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety disorder | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4924c2cf-ffe0-7398-e054-00144ff88e88 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety disorder | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4924c2cf-ffe0-7398-e054-00144ff88e88 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety disorder | PROCHLORPERAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4924c2cf-ffe0-7398-e054-00144ff88e88 | 1 | LoF | protect | |||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | sleep apnea | KETAMINE | targetBased | 4 | Recruiting | 23/07/2020 | https://clinicaltrials.gov/study/NCT04452383 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | delirium | KETAMINE | targetBased | 4 | Recruiting | 25/08/2023 | https://clinicaltrials.gov/study/NCT06010927 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | delirium | KETAMINE | targetBased | 4 | Not yet recruiting | 15/05/2023 | https://clinicaltrials.gov/study/NCT05821972 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | delirium | KETAMINE | targetBased | 4 | Completed | 01/07/2013 | https://clinicaltrials.gov/study/NCT02433041 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | delirium | KETAMINE | targetBased | 3 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT01690988 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | acute stress reaction | KETAMINE | targetBased | 4 | Active, not recruiting | 15/04/2020 | https://clinicaltrials.gov/study/NCT04769297 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar I disorder | KETAMINE | targetBased | 4 | Completed | 01/06/2017 | https://clinicaltrials.gov/study/NCT03156504 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | KETAMINE | targetBased | 4 | Completed | 01/06/2010 | https://clinicaltrials.gov/study/NCT01140620 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | KETAMINE | targetBased | 4 | Not yet recruiting | 24/05/2019 | https://clinicaltrials.gov/study/NCT03829124 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | opioid dependence | KETAMINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00300794 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | opioid dependence | KETAMINE | targetBased | 3 | Active, not recruiting | 25/11/2017 | https://clinicaltrials.gov/study/NCT03345173 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | KETAMINE | targetBased | 3 | Suspended | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329394 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE | targetBased | 4 | Recruiting | 22/07/2022 | https://clinicaltrials.gov/study/NCT05487885 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE | targetBased | 4 | Unknown status | 01/07/2014 | https://clinicaltrials.gov/study/NCT02267980 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE | targetBased | 4 | Enrolling by invitation | 01/10/2023 | https://clinicaltrials.gov/study/NCT06034821 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE | targetBased | 4 | Unknown status | 01/09/2016 | https://clinicaltrials.gov/study/NCT02924090 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE | targetBased | 4 | Completed | 01/09/2021 | https://clinicaltrials.gov/study/NCT05026203 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE | targetBased | 4 | Withdrawn | 01/09/2022 | https://clinicaltrials.gov/study/NCT04220125 | 1 | LoF | protect | No enrollment | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | pain agnosia | KETAMINE | targetBased | 4 | Not yet recruiting | 01/12/2024 | https://clinicaltrials.gov/study/NCT06408974 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | unipolar depression | KETAMINE | targetBased | 4 | Completed | 01/06/2010 | https://clinicaltrials.gov/study/NCT01881763 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | unipolar depression | KETAMINE | targetBased | 4 | Completed | 01/06/2017 | https://clinicaltrials.gov/study/NCT03156504 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | KETAMINE | targetBased | 3 | Suspended | 29/10/2018 | https://clinicaltrials.gov/study/NCT03674671 | 0.7 | LoF | protect | insufficient funding | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | KETAMINE | targetBased | 4 | Completed | 01/06/2017 | https://clinicaltrials.gov/study/NCT03156504 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | KETAMINE | targetBased | 4 | Completed | 01/06/2010 | https://clinicaltrials.gov/study/NCT01881763 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | KETAMINE | targetBased | 4 | Completed | 01/03/2013 | https://clinicaltrials.gov/study/NCT01833897 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | KETAMINE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT00947791 | 1 | LoF | protect | Change in available resources for study procedures | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | treatment resistant depression | KETAMINE | targetBased | 4 | Completed | 22/10/2020 | https://clinicaltrials.gov/study/NCT04504175 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | treatment resistant depression | KETAMINE | targetBased | 4 | Recruiting | 03/06/2024 | https://clinicaltrials.gov/study/NCT06278779 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | treatment resistant depression | KETAMINE | targetBased | 4 | Withdrawn | 01/03/2008 | https://clinicaltrials.gov/study/NCT00646087 | 1 | LoF | protect | Pilot study determined that this study would not be feasible. | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | treatment resistant depression | KETAMINE | targetBased | 4 | Unknown status | 01/06/2016 | https://clinicaltrials.gov/study/NCT02772211 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | treatment resistant depression | KETAMINE | targetBased | 4 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01935115 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | treatment resistant depression | KETAMINE | targetBased | 4 | Recruiting | 01/09/2017 | https://clinicaltrials.gov/study/NCT03272698 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | mental or behavioural disorder | KETAMINE | targetBased | 4 | Completed | 15/06/2019 | https://clinicaltrials.gov/study/NCT05320991 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | mental or behavioural disorder | KETAMINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00205712 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | postpartum depression | KETAMINE | targetBased | 4 | Completed | 23/11/2017 | https://clinicaltrials.gov/study/NCT03336541 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | postpartum depression | KETAMINE | targetBased | 4 | Not yet recruiting | 01/12/2019 | https://clinicaltrials.gov/study/NCT03927378 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | postpartum depression | KETAMINE | targetBased | 3 | Completed | 12/11/2020 | https://clinicaltrials.gov/study/NCT04227704 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | obstructive sleep apnea | KETAMINE | targetBased | 4 | Completed | 01/12/2014 | https://clinicaltrials.gov/study/NCT02425202 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive episode | KETAMINE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00680433 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | KETAMINE | targetBased | 4 | Completed | 22/08/2019 | https://clinicaltrials.gov/study/NCT03861988 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | KETAMINE | targetBased | 4 | Recruiting | 13/10/2022 | https://clinicaltrials.gov/study/NCT05450432 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | KETAMINE | targetBased | 4 | Completed | 01/03/2016 | https://clinicaltrials.gov/study/NCT02544607 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | KETAMINE | targetBased | 4 | Completed | 09/10/2020 | https://clinicaltrials.gov/study/NCT04091971 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | KETAMINE | targetBased | 4 | Recruiting | 31/01/2024 | https://clinicaltrials.gov/study/NCT06213324 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | KETAMINE | targetBased | 4 | Completed | 01/10/2015 | https://clinicaltrials.gov/study/NCT02579928 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | KETAMINE | targetBased | 4 | Terminated | 01/11/2010 | https://clinicaltrials.gov/study/NCT01260649 | 1 | LoF | protect | lack of funding to cover staff salary (clinician and research coordinator) | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol withdrawal | KETAMINE | targetBased | 4 | Withdrawn | 01/02/2018 | https://clinicaltrials.gov/study/NCT02823977 | 1 | LoF | protect | Funding not obtained | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol withdrawal | KETAMINE | targetBased | 4 | Withdrawn | 12/04/2019 | https://clinicaltrials.gov/study/NCT03788889 | 1 | LoF | protect | internal practice and policy limitations including time commitment / workflow issues | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Agitation | KETAMINE | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02909465 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Agitation | KETAMINE | targetBased | 4 | Withdrawn | 01/04/2014 | https://clinicaltrials.gov/study/NCT02103881 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Agitation | KETAMINE | targetBased | 4 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT02022488 | 1 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUTORPHANOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9822ca3f-aee2-46e5-8a96-495400e65d10 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUTORPHANOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9822ca3f-aee2-46e5-8a96-495400e65d10 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUTORPHANOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b8e48063-0b40-ee43-85c1-4ef2de80c404 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUTORPHANOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b8e48063-0b40-ee43-85c1-4ef2de80c404 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUTORPHANOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9822ca3f-aee2-46e5-8a96-495400e65d10 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUTORPHANOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b8e48063-0b40-ee43-85c1-4ef2de80c404 | 1 | GoF | protect | |||
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | ESR1 | Estrogen receptor, Estrogen receptor | bipolar disorder | TAMOXIFEN CITRATE | targetBased | 3 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00411203 | 0.7 | protect | ||
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | ESR1 | Estrogen receptor, Estrogen receptor | bipolar disorder | TAMOXIFEN CITRATE | targetBased | 3 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00411203 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | post-traumatic stress disorder | METHYLPHENIDATE | targetBased | 4 | Recruiting | 05/02/2024 | https://clinicaltrials.gov/study/NCT05776056 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Williams syndrome | METHYLPHENIDATE | targetBased | 4 | Recruiting | 01/05/2001 | https://clinicaltrials.gov/study/NCT00768820 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obsessive-compulsive disorder | METHYLPHENIDATE | targetBased | 4 | Completed | 01/10/2013 | https://clinicaltrials.gov/study/NCT02194075 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Dementia | METHYLPHENIDATE | targetBased | 4 | Terminated | 01/11/2012 | https://clinicaltrials.gov/study/NCT01825577 | 1 | LoF | protect | Administrative Reasons |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Dementia | METHYLPHENIDATE | targetBased | 3 | Unknown status | 01/05/2012 | https://clinicaltrials.gov/study/NCT01599975 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | METHYLPHENIDATE | targetBased | 4 | Completed | 01/02/2008 | https://clinicaltrials.gov/study/NCT00602290 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | METHYLPHENIDATE | targetBased | 3 | Terminated | 01/04/2002 | https://clinicaltrials.gov/study/NCT00031798 | 0.7 | LoF | protect | low accrual; loss of funding |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | METHYLPHENIDATE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01497548 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | METHYLPHENIDATE | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00253747 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | METHYLPHENIDATE | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00246233 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | METHYLPHENIDATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ec8a8896-077d-4dee-9e10-97172512c5ed | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | METHYLPHENIDATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cd83fc91-47a3-4be4-9727-caf9ec0371e8 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | METHYLPHENIDATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c0bf0835-6a2f-4067-a158-8b86c4b0668a | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | METHYLPHENIDATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9e3c22d9-71d9-46a7-b315-8021c94c4bec | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | delirium | METHYLPHENIDATE | targetBased | 3 | Terminated | 01/02/2008 | https://clinicaltrials.gov/study/NCT00599287 | 0.7 | LoF | protect | Inclusion rate too low due to a lack of eligible patients and difficulties obtaining informed consent. |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | anxiety | METHYLPHENIDATE | targetBased | 4 | Completed | 16/06/2014 | https://clinicaltrials.gov/study/NCT02153944 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar disorder | METHYLPHENIDATE | targetBased | 3 | Completed | 01/03/2012 | https://clinicaltrials.gov/study/NCT01541605 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE | targetBased | 4 | Completed | 17/04/2012 | https://clinicaltrials.gov/study/NCT01552915 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE | targetBased | 4 | Recruiting | 27/07/2021 | https://clinicaltrials.gov/study/NCT04781972 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE | targetBased | 4 | Unknown status | 01/09/2016 | https://clinicaltrials.gov/study/NCT02677519 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f63155b9-ea71-4a30-be32-37173f87bcbf | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE | targetBased | 4 | Terminated | 03/08/2021 | https://clinicaltrials.gov/study/NCT04987762 | 1 | LoF | protect | due to administrative reasons not related to efficacy or safety. |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE | targetBased | 4 | Completed | 01/11/2008 | https://clinicaltrials.gov/study/NCT00778310 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE | targetBased | 4 | Completed | 01/09/2015 | https://clinicaltrials.gov/study/NCT02473185 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | GEPIRONE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/021164s000lbl.pdf | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | GEPIRONE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/021164s000lbl.pdf | 1 | GoF | protect | |||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | delirium | MEMANTINE | targetBased | 4 | Terminated | 01/03/2006 | https://clinicaltrials.gov/study/NCT00303433 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | eating disorder | MEMANTINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00330655 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | attention deficit hyperactivity disorder | MEMANTINE | targetBased | 4 | Completed | 01/03/2007 | https://clinicaltrials.gov/study/NCT00586573 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | post-traumatic stress disorder | MEMANTINE | targetBased | 4 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT02258828 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1fa2b7bc-94e5-4566-a7c5-419f8fd393a7 | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE | targetBased | 4 | Completed | 01/09/2007 | https://clinicaltrials.gov/study/NCT00371059 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE | targetBased | 4 | Completed | 01/11/2004 | https://clinicaltrials.gov/study/NCT00768261 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b9f27baf-aa2a-443a-9ef5-e002d23407ba | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c8f5c20b-4573-44c5-89fc-4da11b2e1fe1 | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=81496236-0a90-4265-8244-cba6a6b4f3ac | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06DX01 | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | MEMANTINE | targetBased | 3 | Unknown status | 01/01/2014 | https://clinicaltrials.gov/study/NCT02001103 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | MEMANTINE | targetBased | 3 | Terminated | 01/04/2004 | https://clinicaltrials.gov/study/NCT00148616 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | MEMANTINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | MEMANTINE | targetBased | 3 | Terminated | 01/11/2005 | https://clinicaltrials.gov/study/NCT00148590 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | MEMANTINE | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00757978 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | anxiety | MEMANTINE | targetBased | 3 | Completed | 01/12/2006 | https://clinicaltrials.gov/study/NCT00411398 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | anxiety | MEMANTINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | MEMANTINE | targetBased | 4 | Completed | 01/10/2013 | https://clinicaltrials.gov/study/NCT01902004 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | MEMANTINE | targetBased | 3 | Completed | 01/06/2002 | https://clinicaltrials.gov/study/NCT00040261 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | MEMANTINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | MEMANTINE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00183729 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | MEMANTINE | targetBased | 4 | Completed | 01/06/2006 | https://clinicaltrials.gov/study/NCT00344682 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Pick disease | MEMANTINE | targetBased | 4 | Completed | 01/05/2004 | https://clinicaltrials.gov/study/NCT00187525 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | MEMANTINE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00305578 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | MEMANTINE | targetBased | 3 | Unknown status | 01/01/2013 | https://clinicaltrials.gov/study/NCT03039842 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | MEMANTINE | targetBased | 4 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00586066 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | learning disability | MEMANTINE | targetBased | 3 | Recruiting | 13/11/2018 | https://clinicaltrials.gov/study/NCT03553875 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | autism spectrum disorder | MEMANTINE | targetBased | 4 | Completed | 01/01/2010 | https://clinicaltrials.gov/study/NCT01333865 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | autism spectrum disorder | MEMANTINE | targetBased | 3 | Recruiting | 13/11/2018 | https://clinicaltrials.gov/study/NCT03553875 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | autism spectrum disorder | MEMANTINE | targetBased | 3 | Completed | 17/02/2015 | https://clinicaltrials.gov/study/NCT01972074 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | autism | MEMANTINE | targetBased | 3 | Recruiting | 13/11/2018 | https://clinicaltrials.gov/study/NCT03553875 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | obsessive-compulsive disorder | MEMANTINE | targetBased | 3 | Not yet recruiting | 01/09/2021 | https://clinicaltrials.gov/study/NCT05015595 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | substance abuse | MEMANTINE | targetBased | 3 | Completed | 01/03/2009 | https://clinicaltrials.gov/study/NCT01189214 | 0.7 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | ZIMELDINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AB02 | 1 | LoF | protect | |||
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | unipolar depression | ZIMELDINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AB02 | 1 | LoF | protect | |||
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | unipolar depression | ZIMELDINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AB02 | 1 | LoF | protect | |||
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | unipolar depression | ZIMELDINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AB02 | 1 | LoF | protect | |||
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | unipolar depression | ZIMELDINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AB02 | 1 | LoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | ZIMELDINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AB02 | 1 | LoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | ZIMELDINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AB02 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7c552f11-e24a-4d9b-bb8d-be10c928eca8 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE | targetBased | 4 | Recruiting | 24/05/2023 | https://clinicaltrials.gov/study/NCT05721235 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE | targetBased | 4 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00776009 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d334e2f1-7497-4131-a5c0-7ac30d4741cb | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cad21255-f17f-4744-b20d-76d138ca5df2 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE | targetBased | 4 | Active, not recruiting | 22/03/2023 | https://clinicaltrials.gov/study/NCT05685732 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dd659d39-41f5-4612-8f17-bad602b4784d | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | delirium | LOXAPINE | targetBased | 3 | Terminated | 09/04/2023 | https://clinicaltrials.gov/study/NCT05324852 | 0.7 | LoF | protect | Sponsor decision: |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | LOXAPINE | targetBased | 4 | Terminated | 30/09/2017 | https://clinicaltrials.gov/study/NCT03110900 | 1 | LoF | protect | Sponsor Withdrawal |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | LOXAPINE | targetBased | 3 | Completed | 01/07/2008 | https://clinicaltrials.gov/study/NCT00721955 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b074f950-246a-41f0-aedf-32f38998a4b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b074f950-246a-41f0-aedf-32f38998a4b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b074f950-246a-41f0-aedf-32f38998a4b1 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Agitation | LOXAPINE | targetBased | 4 | Terminated | 30/09/2017 | https://clinicaltrials.gov/study/NCT03110900 | 1 | LoF | protect | Sponsor Withdrawal |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Agitation | LOXAPINE | targetBased | 4 | Terminated | 30/09/2017 | https://clinicaltrials.gov/study/NCT03110900 | 1 | LoF | protect | Sponsor Withdrawal |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | LOXAPINE | targetBased | 4 | Terminated | 30/09/2017 | https://clinicaltrials.gov/study/NCT03110900 | 1 | LoF | protect | Sponsor Withdrawal |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/adasuve | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | LOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH01 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | LOXAPINE | targetBased | 3 | Completed | 01/07/2008 | https://clinicaltrials.gov/study/NCT00721955 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | LOXAPINE | targetBased | 3 | Completed | 01/07/2008 | https://clinicaltrials.gov/study/NCT00721955 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar I disorder | LOXAPINE | targetBased | 3 | Completed | 01/07/2008 | https://clinicaltrials.gov/study/NCT00721955 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LOXAPINE | targetBased | 3 | Completed | 01/07/2008 | https://clinicaltrials.gov/study/NCT00721955 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b074f950-246a-41f0-aedf-32f38998a4b1 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | LOXAPINE | targetBased | 4 | Terminated | 30/09/2017 | https://clinicaltrials.gov/study/NCT03110900 | 1 | LoF | protect | Sponsor Withdrawal |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=257148b5-869e-4a06-89ca-8b8686e8e528 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=613a6459-0e61-4bed-9138-2836ff49f40b | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety | LOXAPINE | targetBased | 3 | Terminated | 01/12/2005 | https://clinicaltrials.gov/study/NCT00290082 | 0.35 | LoF | protect | 2 complications with midazolam |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | LOPERAMIDE | targetBased | 4 | Completed | 01/01/2014 | https://clinicaltrials.gov/study/NCT03017430 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | LOPERAMIDE | targetBased | 4 | Completed | 01/01/2014 | https://clinicaltrials.gov/study/NCT03017430 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | BENPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD07 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | BENPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD07 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | BENPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD07 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | BENPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD07 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | BENPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD07 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | BENPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD07 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BENPERIDOL | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BENPERIDOL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | FLUSPIRILENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | FLUSPIRILENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | FLUSPIRILENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG01 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | FLUSPIRILENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | FLUSPIRILENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG01 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | FLUSPIRILENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG01 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUSPIRILENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUSPIRILENE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | methamphetamine-induced psychosis | CINNARIZINE | targetBased | 4 | Completed | 01/03/2010 | https://clinicaltrials.gov/study/NCT01939093 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUTORPHANOL TARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9822ca3f-aee2-46e5-8a96-495400e65d10 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUTORPHANOL TARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9822ca3f-aee2-46e5-8a96-495400e65d10 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUTORPHANOL TARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b8e48063-0b40-ee43-85c1-4ef2de80c404 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUTORPHANOL TARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b8e48063-0b40-ee43-85c1-4ef2de80c404 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUTORPHANOL TARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b8e48063-0b40-ee43-85c1-4ef2de80c404 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUTORPHANOL TARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9822ca3f-aee2-46e5-8a96-495400e65d10 | 1 | GoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | treatment resistant depression | BUPROPION | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | treatment resistant depression | BUPROPION | targetBased | 3 | Completed | 08/07/2019 | https://clinicaltrials.gov/study/NCT04039022 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizoaffective disorder | BUPROPION | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00320723 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | smoking behavior | BUPROPION | targetBased | 3 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00033592 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Dementia | BUPROPION | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar I disorder | BUPROPION | targetBased | 3 | Completed | 01/11/2010 | https://clinicaltrials.gov/study/NCT00958633 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION | targetBased | 4 | Unknown status | 01/06/2004 | https://clinicaltrials.gov/study/NCT00106197 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00181896 | 1 | LoF | protect | Study was terminated due to lack of recruitment |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fddb7191-c4f9-4e82-bd7d-259c3767710a | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION | targetBased | 4 | Terminated | 23/07/2019 | https://clinicaltrials.gov/study/NCT03993457 | 1 | LoF | protect | terminated during COVID due to inability to see participants in person. |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06d4d890-11ed-4f31-8778-c73432e3ea69 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION | targetBased | 4 | Completed | 01/01/2007 | https://clinicaltrials.gov/study/NCT03927950 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION | targetBased | 4 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00178828 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | methamphetamine dependence | BUPROPION | targetBased | 3 | Completed | 05/05/2017 | https://clinicaltrials.gov/study/NCT03078075 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT01621009 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION | targetBased | 4 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00484692 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION | targetBased | 4 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00332644 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02245308 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT01621022 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION | targetBased | 4 | Completed | 01/07/2009 | https://clinicaltrials.gov/study/NCT00991081 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION | targetBased | 4 | Terminated | 01/03/2005 | https://clinicaltrials.gov/study/NCT00119210 | 1 | LoF | protect | We were unable to recruit sufficient numbers of patients and decided that the study protocol was not feasible to implement |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | BUPROPION | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00320723 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | BUPROPION | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fddb7191-c4f9-4e82-bd7d-259c3767710a | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION | targetBased | 4 | Recruiting | 27/12/2023 | https://clinicaltrials.gov/study/NCT06223880 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION | targetBased | 4 | Not yet recruiting | 01/06/2023 | https://clinicaltrials.gov/study/NCT02129751 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION | targetBased | 4 | Recruiting | 30/09/2022 | https://clinicaltrials.gov/study/NCT05537584 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=02500709-7f2c-4251-bd8c-94ab6cdadd4c | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION | targetBased | 4 | Withdrawn | 15/10/2020 | https://clinicaltrials.gov/study/NCT04388189 | 1 | LoF | protect | No participants enrolled |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION | targetBased | 4 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00316160 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | dysthymic disorder | BUPROPION | targetBased | 4 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00296777 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | dysthymic disorder | BUPROPION | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | LoF | protect | No participants enrolled. |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | dysthymic disorder | BUPROPION | targetBased | 4 | Completed | 01/11/2004 | https://clinicaltrials.gov/study/NCT00225251 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | dysthymic disorder | BUPROPION | targetBased | 4 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00296712 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | dysthymic disorder | BUPROPION | targetBased | 4 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00404755 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | mood disorder | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06d4d890-11ed-4f31-8778-c73432e3ea69 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | anxiety | BUPROPION | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar disorder | BUPROPION | targetBased | 4 | Unknown status | 01/04/2014 | https://clinicaltrials.gov/study/NCT01583023 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar disorder | BUPROPION | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00177567 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar disorder | BUPROPION | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00181896 | 1 | LoF | protect | Study was terminated due to lack of recruitment |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | substance dependence | BUPROPION | targetBased | 4 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00484692 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=10a64abf-9704-4abb-98fb-bca228cab93a | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=82f5292b-b113-4f10-9469-04386fa8e9d4 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5d229da8-aa9b-4760-90e1-bf10b849e054 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee3f124-bc24-4a37-b2eb-501a66fef064 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=332403a7-3138-4f58-a33b-37fd3d573177 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX12 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0a7eb657-e991-4243-8165-58e506180a9e | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | BUPROPION | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00048360 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | substance abuse | BUPROPION | targetBased | 4 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00484692 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | NALBUPHINE | targetBased | 4 | Recruiting | 01/03/2022 | https://clinicaltrials.gov/study/NCT05273671 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | NALBUPHINE | targetBased | 4 | Recruiting | 01/03/2022 | https://clinicaltrials.gov/study/NCT05273671 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | NALBUPHINE | targetBased | 4 | Recruiting | 01/05/2023 | https://clinicaltrials.gov/study/NCT05769530 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | NALBUPHINE | targetBased | 4 | Recruiting | 01/05/2023 | https://clinicaltrials.gov/study/NCT05769530 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | NALBUPHINE | targetBased | 3 | Not yet recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06306040 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | NALBUPHINE | targetBased | 3 | Not yet recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06306040 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | Agitation | NALBUPHINE | targetBased | 4 | Recruiting | 01/05/2023 | https://clinicaltrials.gov/study/NCT05769530 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | Agitation | NALBUPHINE | targetBased | 4 | Recruiting | 01/03/2022 | https://clinicaltrials.gov/study/NCT05273671 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | delirium | NALBUPHINE | targetBased | 3 | Not yet recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06306040 | 0.7 | GoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=77342716-6dd7-488d-bfa4-9637feb4b5f0 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dd659d39-41f5-4612-8f17-bad602b4784d | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c7beed0d-a4cb-4c4d-933a-c17c4bab6ef1 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cad21255-f17f-4744-b20d-76d138ca5df2 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1ebab71b-5b74-4705-ba05-4734f1c4561f | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d334e2f1-7497-4131-a5c0-7ac30d4741cb | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXMETHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=694ebbf3-966b-4c0d-8d3c-ed95ee0dc8cb | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | CHLORPROTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF03 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety | CHLORPROTHIXENE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | Tourette syndrome | ECOPIPAM | targetBased | 3 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT06021522 | 0.7 | LoF | protect | |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | Tourette syndrome | ECOPIPAM | targetBased | 3 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT06021522 | 0.7 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | Tourette syndrome | ECOPIPAM | targetBased | 3 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT06021522 | 0.7 | LoF | protect | |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | Tourette syndrome | ECOPIPAM | targetBased | 3 | Recruiting | 31/01/2023 | https://clinicaltrials.gov/study/NCT05615220 | 0.7 | LoF | protect | |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | Tourette syndrome | ECOPIPAM | targetBased | 3 | Recruiting | 31/01/2023 | https://clinicaltrials.gov/study/NCT05615220 | 0.7 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | Tourette syndrome | ECOPIPAM | targetBased | 3 | Recruiting | 31/01/2023 | https://clinicaltrials.gov/study/NCT05615220 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02397837 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02397837 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02397837 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT00597896 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT00597896 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT00597896 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | eating disorder | PRAMIPEXOLE | targetBased | 3 | Withdrawn | 01/04/2010 | https://clinicaltrials.gov/study/NCT01106053 | 0.7 | GoF | protect | No participants were recruited and study has been closed. |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | eating disorder | PRAMIPEXOLE | targetBased | 3 | Withdrawn | 01/04/2010 | https://clinicaltrials.gov/study/NCT01106053 | 0.7 | GoF | protect | No participants were recruited and study has been closed. |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | eating disorder | PRAMIPEXOLE | targetBased | 3 | Withdrawn | 01/04/2010 | https://clinicaltrials.gov/study/NCT01106053 | 0.7 | GoF | protect | No participants were recruited and study has been closed. |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | treatment resistant depression | PRAMIPEXOLE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | treatment resistant depression | PRAMIPEXOLE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | treatment resistant depression | PRAMIPEXOLE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT00597896 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02397837 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02397837 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02397837 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02397837 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02397837 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/10/2014 | https://clinicaltrials.gov/study/NCT02397837 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | PRAMIPEXOLE | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00681863 | 0.7 | GoF | protect | Terminated for slow enrollment. |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | PRAMIPEXOLE | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00681863 | 0.7 | GoF | protect | Terminated for slow enrollment. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | PRAMIPEXOLE | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00681863 | 0.7 | GoF | protect | Terminated for slow enrollment. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | PRAMIPEXOLE | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00681863 | 0.7 | GoF | protect | Terminated for slow enrollment. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | PRAMIPEXOLE | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00681863 | 0.7 | GoF | protect | Terminated for slow enrollment. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | PRAMIPEXOLE | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00681863 | 0.7 | GoF | protect | Terminated for slow enrollment. |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | post-traumatic stress disorder | PRAMIPEXOLE | targetBased | 3 | Terminated | 19/02/2019 | https://clinicaltrials.gov/study/NCT03765138 | 0.7 | GoF | protect | Patient recruitment difficulties |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | post-traumatic stress disorder | PRAMIPEXOLE | targetBased | 3 | Terminated | 19/02/2019 | https://clinicaltrials.gov/study/NCT03765138 | 0.7 | GoF | protect | Patient recruitment difficulties |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | post-traumatic stress disorder | PRAMIPEXOLE | targetBased | 3 | Terminated | 19/02/2019 | https://clinicaltrials.gov/study/NCT03765138 | 0.7 | GoF | protect | Patient recruitment difficulties |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02033369 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02033369 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02033369 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02033369 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02033369 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02033369 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | major depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02033369 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | major depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02033369 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | major depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02033369 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PRAMIPEXOLE | targetBased | 3 | Terminated | 19/02/2019 | https://clinicaltrials.gov/study/NCT03765138 | 0.7 | GoF | protect | Patient recruitment difficulties |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PRAMIPEXOLE | targetBased | 3 | Terminated | 19/02/2019 | https://clinicaltrials.gov/study/NCT03765138 | 0.7 | GoF | protect | Patient recruitment difficulties |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PRAMIPEXOLE | targetBased | 3 | Terminated | 19/02/2019 | https://clinicaltrials.gov/study/NCT03765138 | 0.7 | GoF | protect | Patient recruitment difficulties |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PRAMIPEXOLE | targetBased | 3 | Terminated | 19/02/2019 | https://clinicaltrials.gov/study/NCT03765138 | 0.7 | GoF | protect | Patient recruitment difficulties |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PRAMIPEXOLE | targetBased | 3 | Terminated | 19/02/2019 | https://clinicaltrials.gov/study/NCT03765138 | 0.7 | GoF | protect | Patient recruitment difficulties |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PRAMIPEXOLE | targetBased | 3 | Terminated | 19/02/2019 | https://clinicaltrials.gov/study/NCT03765138 | 0.7 | GoF | protect | Patient recruitment difficulties |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00231959 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01066897 | 1 | GoF | protect | Lack of funding prevented further recruitment |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01066897 | 1 | GoF | protect | Lack of funding prevented further recruitment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01066897 | 1 | GoF | protect | Lack of funding prevented further recruitment |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01066897 | 1 | GoF | protect | Lack of funding prevented further recruitment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01066897 | 1 | GoF | protect | Lack of funding prevented further recruitment |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01066897 | 1 | GoF | protect | Lack of funding prevented further recruitment |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | eating disorder | PRAMIPEXOLE | targetBased | 3 | Withdrawn | 01/04/2010 | https://clinicaltrials.gov/study/NCT01106053 | 0.7 | GoF | protect | No participants were recruited and study has been closed. |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | eating disorder | PRAMIPEXOLE | targetBased | 3 | Withdrawn | 01/04/2010 | https://clinicaltrials.gov/study/NCT01106053 | 0.7 | GoF | protect | No participants were recruited and study has been closed. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | eating disorder | PRAMIPEXOLE | targetBased | 3 | Withdrawn | 01/04/2010 | https://clinicaltrials.gov/study/NCT01106053 | 0.7 | GoF | protect | No participants were recruited and study has been closed. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | eating disorder | PRAMIPEXOLE | targetBased | 3 | Withdrawn | 01/04/2010 | https://clinicaltrials.gov/study/NCT01106053 | 0.7 | GoF | protect | No participants were recruited and study has been closed. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | eating disorder | PRAMIPEXOLE | targetBased | 3 | Withdrawn | 01/04/2010 | https://clinicaltrials.gov/study/NCT01106053 | 0.7 | GoF | protect | No participants were recruited and study has been closed. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | eating disorder | PRAMIPEXOLE | targetBased | 3 | Withdrawn | 01/04/2010 | https://clinicaltrials.gov/study/NCT01106053 | 0.7 | GoF | protect | No participants were recruited and study has been closed. |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01066897 | 1 | GoF | protect | Lack of funding prevented further recruitment |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01066897 | 1 | GoF | protect | Lack of funding prevented further recruitment |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01066897 | 1 | GoF | protect | Lack of funding prevented further recruitment |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | PRAMIPEXOLE | targetBased | 3 | Recruiting | 21/04/2023 | https://clinicaltrials.gov/study/NCT05825235 | 0.7 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00231959 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00231959 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | PRAMIPEXOLE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00231959 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | PRAMIPEXOLE | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00681863 | 0.7 | GoF | protect | Terminated for slow enrollment. |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | PRAMIPEXOLE | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00681863 | 0.7 | GoF | protect | Terminated for slow enrollment. |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Tourette syndrome | PRAMIPEXOLE | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00681863 | 0.7 | GoF | protect | Terminated for slow enrollment. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | PRAMIPEXOLE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | PRAMIPEXOLE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | PRAMIPEXOLE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | PRAMIPEXOLE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | PRAMIPEXOLE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | PRAMIPEXOLE | targetBased | 4 | Recruiting | 07/08/2021 | https://clinicaltrials.gov/study/NCT04936126 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | PRAMIPEXOLE | targetBased | 3 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01320982 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | OXYMORPHONE | targetBased | 4 | Terminated | 14/09/2016 | https://clinicaltrials.gov/study/NCT02741076 | 1 | GoF | protect | Inability to recruit sufficient no. of subjects over an acceptable time period |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | OXYMORPHONE | targetBased | 4 | Terminated | 14/09/2016 | https://clinicaltrials.gov/study/NCT02741076 | 1 | GoF | protect | Inability to recruit sufficient no. of subjects over an acceptable time period |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | OXYMORPHONE | targetBased | 4 | Terminated | 14/09/2016 | https://clinicaltrials.gov/study/NCT02741076 | 1 | GoF | protect | Inability to recruit sufficient no. of subjects over an acceptable time period |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALMEFENE | targetBased | 4 | Withdrawn | 01/06/2023 | https://clinicaltrials.gov/study/NCT05808881 | 1 | GoF | protect | Due to changes in research objectives and methodological approach. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALMEFENE | targetBased | 3 | Recruiting | 31/03/2023 | https://clinicaltrials.gov/study/NCT05540288 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | NALMEFENE | targetBased | 3 | Recruiting | 31/03/2023 | https://clinicaltrials.gov/study/NCT05540288 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | NALMEFENE | targetBased | 3 | Recruiting | 31/03/2023 | https://clinicaltrials.gov/study/NCT05540288 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALMEFENE | targetBased | 4 | Withdrawn | 01/06/2023 | https://clinicaltrials.gov/study/NCT05808881 | 1 | LoF | protect | Due to changes in research objectives and methodological approach. |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALMEFENE | targetBased | 4 | Withdrawn | 01/06/2023 | https://clinicaltrials.gov/study/NCT05808881 | 1 | LoF | protect | Due to changes in research objectives and methodological approach. |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | Terminated | 01/08/2014 | https://clinicaltrials.gov/study/NCT02195817 | 1 | LoF | protect | The study was terminated due to enrolment challenges |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BB05 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BB05 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/selincro | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/selincro | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | Completed | 01/09/2014 | https://clinicaltrials.gov/study/NCT02197598 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | Completed | 01/09/2014 | https://clinicaltrials.gov/study/NCT02197598 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 3 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT00811720 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BB05 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 3 | Completed | 13/07/2015 | https://clinicaltrials.gov/study/NCT02382276 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 3 | Completed | 01/03/2009 | https://clinicaltrials.gov/study/NCT00811941 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | Terminated | 01/08/2014 | https://clinicaltrials.gov/study/NCT02195817 | 1 | GoF | protect | The study was terminated due to enrolment challenges |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/selincro | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 3 | Completed | 01/03/2009 | https://clinicaltrials.gov/study/NCT00812461 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | NALMEFENE | targetBased | 4 | Completed | 01/09/2014 | https://clinicaltrials.gov/study/NCT02197598 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | CLOTHIAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH06 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | REMIFENTANIL | targetBased | 4 | Not yet recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT06454292 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | REMIFENTANIL | targetBased | 4 | Not yet recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT06454292 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | REMIFENTANIL | targetBased | 4 | Not yet recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT06444997 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | REMIFENTANIL | targetBased | 4 | Not yet recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT06444997 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | REMIFENTANIL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02334046 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | REMIFENTANIL | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02334046 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | REMIFENTANIL | targetBased | 4 | Completed | 16/11/2017 | https://clinicaltrials.gov/study/NCT03330782 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | REMIFENTANIL | targetBased | 4 | Completed | 16/11/2017 | https://clinicaltrials.gov/study/NCT03330782 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | REMIFENTANIL | targetBased | 4 | Completed | 01/10/2013 | https://clinicaltrials.gov/study/NCT01931683 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | REMIFENTANIL | targetBased | 4 | Completed | 01/10/2013 | https://clinicaltrials.gov/study/NCT01931683 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | REMIFENTANIL | targetBased | 4 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02428283 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | REMIFENTANIL | targetBased | 4 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02428283 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | REMIFENTANIL | targetBased | 4 | Unknown status | 01/04/2014 | https://clinicaltrials.gov/study/NCT02104297 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | REMIFENTANIL | targetBased | 4 | Unknown status | 01/04/2014 | https://clinicaltrials.gov/study/NCT02104297 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | REMIFENTANIL | targetBased | 4 | Not yet recruiting | 15/11/2022 | https://clinicaltrials.gov/study/NCT05624424 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | REMIFENTANIL | targetBased | 4 | Not yet recruiting | 15/11/2022 | https://clinicaltrials.gov/study/NCT05624424 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | REMIFENTANIL | targetBased | 4 | Unknown status | 01/07/2014 | https://clinicaltrials.gov/study/NCT02078583 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | REMIFENTANIL | targetBased | 4 | Unknown status | 01/07/2014 | https://clinicaltrials.gov/study/NCT02078583 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | REMIFENTANIL | targetBased | 4 | Completed | 01/07/2012 | https://clinicaltrials.gov/study/NCT01895348 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | REMIFENTANIL | targetBased | 4 | Completed | 01/07/2012 | https://clinicaltrials.gov/study/NCT01895348 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | REMIFENTANIL | targetBased | 4 | Completed | 01/01/2012 | https://clinicaltrials.gov/study/NCT01495377 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | REMIFENTANIL | targetBased | 4 | Completed | 01/01/2012 | https://clinicaltrials.gov/study/NCT01495377 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | REMIFENTANIL | targetBased | 3 | Terminated | 29/11/2017 | https://clinicaltrials.gov/study/NCT03316339 | 0.7 | GoF | protect | Sponsor's decision |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | REMIFENTANIL | targetBased | 4 | Unknown status | 11/01/2019 | https://clinicaltrials.gov/study/NCT03812003 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | REMIFENTANIL | targetBased | 4 | Unknown status | 11/01/2019 | https://clinicaltrials.gov/study/NCT03812003 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | REMIFENTANIL | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | REMIFENTANIL | targetBased | 4 | Completed | 01/10/2010 | https://clinicaltrials.gov/study/NCT01191645 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | dysthymic disorder | LEVODOPA | targetBased | 4 | Terminated | 09/01/2019 | https://clinicaltrials.gov/study/NCT03761030 | 1 | GoF | protect | The project end date was reached prior to the full sample enrollment |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | dysthymic disorder | LEVODOPA | targetBased | 4 | Terminated | 09/01/2019 | https://clinicaltrials.gov/study/NCT03761030 | 1 | GoF | protect | The project end date was reached prior to the full sample enrollment |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | dysthymic disorder | LEVODOPA | targetBased | 4 | Terminated | 09/01/2019 | https://clinicaltrials.gov/study/NCT03761030 | 1 | GoF | protect | The project end date was reached prior to the full sample enrollment |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | impulse control disorder | LEVODOPA | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01683253 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | impulse control disorder | LEVODOPA | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01683253 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | impulse control disorder | LEVODOPA | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01683253 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | post-traumatic stress disorder | LEVODOPA | targetBased | 4 | Completed | 01/03/2016 | https://clinicaltrials.gov/study/NCT02560389 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | post-traumatic stress disorder | LEVODOPA | targetBased | 4 | Completed | 01/03/2016 | https://clinicaltrials.gov/study/NCT02560389 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | post-traumatic stress disorder | LEVODOPA | targetBased | 4 | Completed | 01/03/2016 | https://clinicaltrials.gov/study/NCT02560389 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | major depressive disorder | LEVODOPA | targetBased | 4 | Terminated | 09/01/2019 | https://clinicaltrials.gov/study/NCT03761030 | 1 | GoF | protect | The project end date was reached prior to the full sample enrollment |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | major depressive disorder | LEVODOPA | targetBased | 4 | Terminated | 09/01/2019 | https://clinicaltrials.gov/study/NCT03761030 | 1 | GoF | protect | The project end date was reached prior to the full sample enrollment |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | major depressive disorder | LEVODOPA | targetBased | 4 | Terminated | 09/01/2019 | https://clinicaltrials.gov/study/NCT03761030 | 1 | GoF | protect | The project end date was reached prior to the full sample enrollment |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | LEVODOPA | targetBased | 4 | Recruiting | 21/11/2023 | https://clinicaltrials.gov/study/NCT06075771 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | LEVODOPA | targetBased | 4 | Terminated | 07/10/2021 | https://clinicaltrials.gov/study/NCT04650217 | 1 | GoF | protect | Study terminated by sponsor (NIMH) |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | LEVODOPA | targetBased | 4 | Terminated | 07/10/2021 | https://clinicaltrials.gov/study/NCT04650217 | 1 | GoF | protect | Study terminated by sponsor (NIMH) |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | LEVODOPA | targetBased | 4 | Terminated | 07/10/2021 | https://clinicaltrials.gov/study/NCT04650217 | 1 | GoF | protect | Study terminated by sponsor (NIMH) |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | LEVODOPA | targetBased | 4 | Completed | 09/10/2015 | https://clinicaltrials.gov/study/NCT02513485 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | LEVODOPA | targetBased | 4 | Completed | 09/10/2015 | https://clinicaltrials.gov/study/NCT02513485 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | LEVODOPA | targetBased | 4 | Completed | 09/10/2015 | https://clinicaltrials.gov/study/NCT02513485 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | dyslexia | LEVODOPA | targetBased | 4 | Unknown status | 01/01/2005 | https://clinicaltrials.gov/study/NCT00111371 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | dyslexia | LEVODOPA | targetBased | 4 | Unknown status | 01/01/2005 | https://clinicaltrials.gov/study/NCT00111371 | 1 | GoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | dyslexia | LEVODOPA | targetBased | 4 | Unknown status | 01/01/2005 | https://clinicaltrials.gov/study/NCT00111371 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Sleep Disorder | VOLINANSERIN | targetBased | 3 | Terminated | 01/04/2007 | https://clinicaltrials.gov/study/NCT00464061 | 0.35 | LoF | protect | Sponsor's decision due to absence of demonstration of efficacy of volinanserin in primary insomnia with predominant sleep maintenance problems |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Sleep Disorder | VOLINANSERIN | targetBased | 3 | Completed | 01/06/2007 | https://clinicaltrials.gov/study/NCT00495885 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Sleep Disorder | VOLINANSERIN | targetBased | 3 | Terminated | 01/11/2008 | https://clinicaltrials.gov/study/NCT00788515 | 0.35 | LoF | protect | Sponsor's decision due to absence of demonstration of efficacy of volinanserin in primary insomnia with predominant sleep maintenance problems |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Sleep Disorder | VOLINANSERIN | targetBased | 3 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00464243 | 0.7 | LoF | protect | |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | VDR | Vitamin D3 receptor | depressive disorder | CHOLECALCIFEROL | targetBased | 4 | Unknown status | 01/03/2011 | https://clinicaltrials.gov/study/NCT01390662 | 1 | GoF | protect | |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | VDR | Vitamin D3 receptor | schizoaffective disorder | CHOLECALCIFEROL | targetBased | 4 | Completed | 01/01/2010 | https://clinicaltrials.gov/study/NCT01169142 | 1 | GoF | protect | |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | VDR | Vitamin D3 receptor | drug dependence | CHOLECALCIFEROL | targetBased | 4 | Recruiting | 11/01/2022 | https://clinicaltrials.gov/study/NCT05161351 | 1 | GoF | protect | |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | VDR | Vitamin D3 receptor | schizophrenia | CHOLECALCIFEROL | targetBased | 4 | Completed | 01/01/2010 | https://clinicaltrials.gov/study/NCT01169142 | 1 | GoF | protect | |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | VDR | Vitamin D3 receptor | schizophrenia | CHOLECALCIFEROL | targetBased | 3 | Not yet recruiting | 15/04/2020 | https://clinicaltrials.gov/study/NCT03284294 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | chronic tic disorder | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | chronic tic disorder | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | chronic tic disorder | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | chronic tic disorder | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | chronic tic disorder | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | chronic tic disorder | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | chronic tic disorder | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | chronic tic disorder | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | chronic tic disorder | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | TIAPRIDE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AL03 | 0.7 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | TIAPRIDE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AL03 | 0.7 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | TIAPRIDE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AL03 | 0.7 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | TIAPRIDE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AL03 | 0.7 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | TIAPRIDE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AL03 | 0.7 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | TIAPRIDE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AL03 | 0.7 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | TIAPRIDE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AL03 | 0.7 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | TIAPRIDE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AL03 | 0.7 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | TIAPRIDE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AL03 | 0.7 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Tourette syndrome | TIAPRIDE | targetBased | 3 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT01501695 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety | TIAPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ACETOPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB07 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ACETOPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB07 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ACETOPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB07 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ACETOPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB07 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ACETOPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB07 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ACETOPHENAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AB07 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | MESORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | MESORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | MESORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | MESORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC03 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | MESORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC03 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | MESORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC03 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | MESORIDAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AC03 | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | cocaine dependence | BIPERIDEN | targetBased | 4 | Unknown status | 01/01/2009 | https://clinicaltrials.gov/study/NCT00495183 | 1 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | cocaine dependence | BIPERIDEN | targetBased | 4 | Unknown status | 01/01/2009 | https://clinicaltrials.gov/study/NCT00495183 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | cocaine dependence | BIPERIDEN | targetBased | 4 | Unknown status | 01/01/2009 | https://clinicaltrials.gov/study/NCT00495183 | 1 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | cocaine dependence | BIPERIDEN | targetBased | 4 | Unknown status | 01/01/2009 | https://clinicaltrials.gov/study/NCT00495183 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | cocaine dependence | BIPERIDEN | targetBased | 4 | Unknown status | 01/01/2009 | https://clinicaltrials.gov/study/NCT00495183 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | cocaine dependence | BIPERIDEN | targetBased | 3 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01251393 | 0.7 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | cocaine dependence | BIPERIDEN | targetBased | 3 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01251393 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | cocaine dependence | BIPERIDEN | targetBased | 3 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01251393 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | anxiety | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | anxiety | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | anxiety | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | anxiety | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | anxiety | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | Dementia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | Dementia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | Dementia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | Dementia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | Dementia | BIPERIDEN | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | DROPERIDOL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD08 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | chronic tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00706589 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | chronic tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00706589 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | chronic tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00706589 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | chronic tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00706589 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | chronic tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00706589 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | chronic tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00706589 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | treatment resistant depression | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | treatment resistant depression | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/05/2009 | https://clinicaltrials.gov/study/NCT00926835 | 1 | LoF | protect | due to patient recruitment difficulties |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01429831 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT00608543 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 10/02/2012 | https://clinicaltrials.gov/study/NCT01696617 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00220636 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | conduct disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 17/11/2004 | https://clinicaltrials.gov/study/NCT00250705 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | conduct disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 17/11/2004 | https://clinicaltrials.gov/study/NCT00250705 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 17/11/2004 | https://clinicaltrials.gov/study/NCT00250705 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | conduct disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 17/11/2004 | https://clinicaltrials.gov/study/NCT00250705 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 17/11/2004 | https://clinicaltrials.gov/study/NCT00250705 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | conduct disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 17/11/2004 | https://clinicaltrials.gov/study/NCT00250705 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | aggressive behavior | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | aggressive behavior | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00440713 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | aggressive behavior | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | aggressive behavior | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | aggressive behavior | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | aggressive behavior | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | aggressive behavior | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | aggressive behavior | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00095524 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT02526030 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT02526030 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism spectrum disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT01028820 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism spectrum disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT01028820 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6875b848-8b13-45f8-ada5-69ef8aece6b6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=217e52b5-3a7b-4bbe-af3c-b18de7d426c3 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=440012b2-4fab-4e2e-ba7f-6ca5558d1e23 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1be1bea7-71d5-406a-bcf3-e1d58f406389 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0424faf3-202f-438a-b65e-2a228790b8f9 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d8275c2d-f42d-4f32-aa9f-03a202c8e99f | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=231e2433-31fe-4612-80f0-ba00dee3b26a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | chronic tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00706589 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c040bd1d-45b7-49f2-93ea-aed7220b30ac | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cbbd3dc0-6a39-48f7-91b9-a95c6c12ee0c | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cbbd3dc0-6a39-48f7-91b9-a95c6c12ee0c | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b6243233-8846-4ea8-a2fa-a563e48fdc29 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b6243233-8846-4ea8-a2fa-a563e48fdc29 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01446328 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00634348 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02146547 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/09/2006 | https://clinicaltrials.gov/study/NCT00395915 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00892047 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00892047 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | ARIPIPRAZOLE | targetBased | 3 | Withdrawn | 01/06/2005 | https://clinicaltrials.gov/study/NCT00276978 | 0.7 | GoF | protect | Initiation of study was stopped due to administrative reasons before first subject was enrolled. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | GoF | protect | Difficulties in recruiting |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | GoF | protect | Difficulties in recruiting |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/12/2014 | https://clinicaltrials.gov/study/NCT02282085 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/21436s04021713s03121729s02321866s025lbl.pdf | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6875b848-8b13-45f8-ada5-69ef8aece6b6 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/12/2007 | https://clinicaltrials.gov/study/NCT00592683 | 1 | GoF | protect | Supply Omega-3 Fatty Acids expired and supplier no longer made same composition. |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/12/2007 | https://clinicaltrials.gov/study/NCT00592683 | 1 | GoF | protect | Supply Omega-3 Fatty Acids expired and supplier no longer made same composition. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/12/2007 | https://clinicaltrials.gov/study/NCT00592683 | 1 | GoF | protect | Supply Omega-3 Fatty Acids expired and supplier no longer made same composition. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/12/2007 | https://clinicaltrials.gov/study/NCT00592683 | 1 | GoF | protect | Supply Omega-3 Fatty Acids expired and supplier no longer made same composition. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/12/2007 | https://clinicaltrials.gov/study/NCT00592683 | 1 | GoF | protect | Supply Omega-3 Fatty Acids expired and supplier no longer made same composition. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/12/2007 | https://clinicaltrials.gov/study/NCT00592683 | 1 | GoF | protect | Supply Omega-3 Fatty Acids expired and supplier no longer made same composition. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | eating disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | eating disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | treatment refractory schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Not yet recruiting | 20/08/2023 | https://clinicaltrials.gov/study/NCT05766540 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | treatment refractory schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Not yet recruiting | 20/08/2023 | https://clinicaltrials.gov/study/NCT05766540 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | chronic tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00706589 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | chronic tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00706589 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | alcohol dependence | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2011 | https://clinicaltrials.gov/study/NCT01292057 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | alcohol dependence | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00082199 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2009 | https://clinicaltrials.gov/study/NCT00728312 | 1 | LoF | protect | PI left the VA. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01813656 | 0.5 | LoF | protect | Aripiprazole arm had obvious adverse reactions,especially akathisia. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2012 | https://clinicaltrials.gov/study/NCT01813643 | 0.5 | LoF | protect | Effects of aripiprazole was not obvious and showed adverse reaction obviously |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202971s008lbl.pdf | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=231e2433-31fe-4612-80f0-ba00dee3b26a | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=231e2433-31fe-4612-80f0-ba00dee3b26a | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8fe516e-25fc-45f6-9a88-542deaa1c3e8 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8fe516e-25fc-45f6-9a88-542deaa1c3e8 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00241176 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d0640208-44e9-4052-a56f-9a4cd9a5aaab | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=12c08d3d-7556-444d-8d01-7737e1507d32 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=12c08d3d-7556-444d-8d01-7737e1507d32 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=634b6431-48ca-480c-a4d8-0ba022bbf0f4 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=634b6431-48ca-480c-a4d8-0ba022bbf0f4 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8fe516e-25fc-45f6-9a88-542deaa1c3e8 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8fe516e-25fc-45f6-9a88-542deaa1c3e8 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | dysthymic disorder | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | LoF | protect | No participants enrolled. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | dysthymic disorder | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | GoF | protect | No participants enrolled. |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | dysthymic disorder | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | GoF | protect | No participants enrolled. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | dysthymic disorder | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | GoF | protect | No participants enrolled. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | dysthymic disorder | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | GoF | protect | No participants enrolled. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | dysthymic disorder | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | GoF | protect | No participants enrolled. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | dysthymic disorder | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | GoF | protect | No participants enrolled. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00095524 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT02526030 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | conduct disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 17/11/2004 | https://clinicaltrials.gov/study/NCT00250705 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00440713 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00440713 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment resistant depression | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00095719 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/05/2009 | https://clinicaltrials.gov/study/NCT00926835 | 1 | GoF | protect | due to patient recruitment difficulties |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01429831 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01429831 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01429831 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01429831 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01429831 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01429831 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | social anxiety disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | social anxiety disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | postpartum depression | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01386086 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00241176 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01727700 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 3 | Completed | 02/05/2018 | https://clinicaltrials.gov/study/NCT03487783 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 3 | Completed | 19/10/2011 | https://clinicaltrials.gov/study/NCT01416441 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | Terminated | 13/10/2018 | https://clinicaltrials.gov/study/NCT03661983 | 1 | LoF | protect | Lack of feasibility for completion of the trial within a reasonable time frame. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2013 | https://clinicaltrials.gov/study/NCT01727713 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 3 | Completed | 27/07/2011 | https://clinicaltrials.gov/study/NCT01418339 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 3 | Completed | 02/08/2011 | https://clinicaltrials.gov/study/NCT01418352 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00440713 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00440713 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00440713 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00440713 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00440713 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00440713 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | GoF | protect | Difficulties in recruiting |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00892047 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00892047 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00892047 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00892047 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00892047 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00892047 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01429831 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01429831 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/05/2017 | https://clinicaltrials.gov/study/NCT02977299 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/05/2017 | https://clinicaltrials.gov/study/NCT02977299 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/05/2009 | https://clinicaltrials.gov/study/NCT00926835 | 1 | GoF | protect | due to patient recruitment difficulties |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/05/2009 | https://clinicaltrials.gov/study/NCT00926835 | 1 | GoF | protect | due to patient recruitment difficulties |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | eating disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=217e52b5-3a7b-4bbe-af3c-b18de7d426c3 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c040bd1d-45b7-49f2-93ea-aed7220b30ac | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c040bd1d-45b7-49f2-93ea-aed7220b30ac | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c040bd1d-45b7-49f2-93ea-aed7220b30ac | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c040bd1d-45b7-49f2-93ea-aed7220b30ac | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c040bd1d-45b7-49f2-93ea-aed7220b30ac | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c040bd1d-45b7-49f2-93ea-aed7220b30ac | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment refractory schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Not yet recruiting | 20/08/2023 | https://clinicaltrials.gov/study/NCT05766540 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2012 | https://clinicaltrials.gov/study/NCT01813643 | 0.5 | GoF | protect | Effects of aripiprazole was not obvious and showed adverse reaction obviously |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2012 | https://clinicaltrials.gov/study/NCT01813643 | 0.5 | GoF | protect | Effects of aripiprazole was not obvious and showed adverse reaction obviously |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2009 | https://clinicaltrials.gov/study/NCT00728312 | 1 | GoF | protect | PI left the VA. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2009 | https://clinicaltrials.gov/study/NCT00728312 | 1 | GoF | protect | PI left the VA. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01813656 | 0.5 | GoF | protect | Aripiprazole arm had obvious adverse reactions,especially akathisia. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01813656 | 0.5 | GoF | protect | Aripiprazole arm had obvious adverse reactions,especially akathisia. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d9fc9628-40da-4eaa-ba7e-412c90abe35c | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d8275c2d-f42d-4f32-aa9f-03a202c8e99f | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d8275c2d-f42d-4f32-aa9f-03a202c8e99f | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d8275c2d-f42d-4f32-aa9f-03a202c8e99f | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d8275c2d-f42d-4f32-aa9f-03a202c8e99f | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d8275c2d-f42d-4f32-aa9f-03a202c8e99f | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d8275c2d-f42d-4f32-aa9f-03a202c8e99f | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00224822 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00224822 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00224822 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00224822 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00224822 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00224822 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | aggressive behavior | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | eating disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | eating disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | eating disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | eating disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | eating disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | eating disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00685334 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ee49f3b1-1650-47ff-9fb1-ea53fe0b92b6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/06/2012 | https://clinicaltrials.gov/study/NCT01710163 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06dda03f-8481-46d6-af02-4f51e1a3a065 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8787c3f-5e41-42d1-8091-44b56346620f | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/08/2012 | https://clinicaltrials.gov/study/NCT01567527 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d8275c2d-f42d-4f32-aa9f-03a202c8e99f | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c005ffe2-ed95-4254-9cfe-4073a09cd718 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=12c08d3d-7556-444d-8d01-7737e1507d32 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6875b848-8b13-45f8-ada5-69ef8aece6b6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/12/2007 | https://clinicaltrials.gov/study/NCT00592683 | 1 | LoF | protect | Supply Omega-3 Fatty Acids expired and supplier no longer made same composition. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=440012b2-4fab-4e2e-ba7f-6ca5558d1e23 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT02305823 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00224822 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00224822 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2006 | https://clinicaltrials.gov/study/NCT00520650 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2006 | https://clinicaltrials.gov/study/NCT00520650 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism spectrum disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT01028820 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Not yet recruiting | 20/08/2023 | https://clinicaltrials.gov/study/NCT05766540 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Not yet recruiting | 20/08/2023 | https://clinicaltrials.gov/study/NCT05766540 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Not yet recruiting | 20/08/2023 | https://clinicaltrials.gov/study/NCT05766540 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Not yet recruiting | 20/08/2023 | https://clinicaltrials.gov/study/NCT05766540 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Not yet recruiting | 20/08/2023 | https://clinicaltrials.gov/study/NCT05766540 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment refractory schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Not yet recruiting | 20/08/2023 | https://clinicaltrials.gov/study/NCT05766540 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2014 | https://clinicaltrials.gov/study/NCT02357849 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2013 | https://clinicaltrials.gov/study/NCT01844700 | 0.5 | LoF | protect | very slow recruitment, no sufficient results |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2009 | https://clinicaltrials.gov/study/NCT01026584 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ARIPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX12 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/05/2010 | https://clinicaltrials.gov/study/NCT01119014 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance abuse | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | substance abuse | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance abuse | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | substance abuse | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance abuse | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | substance abuse | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/01/2007 | https://clinicaltrials.gov/study/NCT00423878 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 21/05/2018 | https://clinicaltrials.gov/study/NCT03568500 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00325689 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/07/2004 | https://clinicaltrials.gov/study/NCT00304655 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/04/2013 | https://clinicaltrials.gov/study/NCT01913327 | 1 | LoF | protect | Insufficient Funds and Inadequate Subject Recruitment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2006 | https://clinicaltrials.gov/study/NCT00520650 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | dysthymic disorder | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | GoF | protect | No participants enrolled. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | dysthymic disorder | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2013 | https://clinicaltrials.gov/study/NCT01942187 | 1 | GoF | protect | No participants enrolled. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bbc2b53b-b712-49eb-b2ce-766bcc448616 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b6243233-8846-4ea8-a2fa-a563e48fdc29 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b6243233-8846-4ea8-a2fa-a563e48fdc29 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=634b6431-48ca-480c-a4d8-0ba022bbf0f4 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=634b6431-48ca-480c-a4d8-0ba022bbf0f4 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8fe516e-25fc-45f6-9a88-542deaa1c3e8 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8fe516e-25fc-45f6-9a88-542deaa1c3e8 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | substance abuse | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | substance abuse | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT00892047 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ARIPIPRAZOLE | targetBased | 3 | Withdrawn | 01/06/2005 | https://clinicaltrials.gov/study/NCT00276978 | 0.7 | LoF | protect | Initiation of study was stopped due to administrative reasons before first subject was enrolled. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148509 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2003 | https://clinicaltrials.gov/study/NCT00556140 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00241176 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00241176 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | Terminated | 13/10/2018 | https://clinicaltrials.gov/study/NCT03661983 | 1 | GoF | protect | Lack of feasibility for completion of the trial within a reasonable time frame. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 4 | Terminated | 13/10/2018 | https://clinicaltrials.gov/study/NCT03661983 | 1 | GoF | protect | Lack of feasibility for completion of the trial within a reasonable time frame. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Tourette syndrome | ARIPIPRAZOLE | targetBased | 3 | Completed | 19/10/2011 | https://clinicaltrials.gov/study/NCT01416441 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/05/2010 | https://clinicaltrials.gov/study/NCT01119014 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2014 | https://clinicaltrials.gov/study/NCT02357849 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/07/2014 | https://clinicaltrials.gov/study/NCT02357849 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2009 | https://clinicaltrials.gov/study/NCT01026584 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/10/2009 | https://clinicaltrials.gov/study/NCT01026584 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ARIPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX12 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01161277 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | alcohol dependence | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2011 | https://clinicaltrials.gov/study/NCT01292057 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | alcohol dependence | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2011 | https://clinicaltrials.gov/study/NCT01292057 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | alcohol dependence | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00082199 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | alcohol dependence | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00082199 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | substance abuse | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00224822 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Completed | 04/01/2017 | https://clinicaltrials.gov/study/NCT02697045 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Completed | 04/01/2017 | https://clinicaltrials.gov/study/NCT02697045 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/aripiprazole-mylan-pharma | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/aripiprazole-mylan-pharma | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1be1bea7-71d5-406a-bcf3-e1d58f406389 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1be1bea7-71d5-406a-bcf3-e1d58f406389 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2005 | https://clinicaltrials.gov/study/NCT00221962 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00305370 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8fe516e-25fc-45f6-9a88-542deaa1c3e8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cbbd3dc0-6a39-48f7-91b9-a95c6c12ee0c | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b6243233-8846-4ea8-a2fa-a563e48fdc29 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6875b848-8b13-45f8-ada5-69ef8aece6b6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0424faf3-202f-438a-b65e-2a228790b8f9 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9648990-0627-4c66-aae1-d3eef398b5b4 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | pervasive developmental disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00870727 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | tic disorder | ARIPIPRAZOLE | targetBased | 4 | Suspended | 01/06/2024 | https://clinicaltrials.gov/study/NCT05361993 | 1 | GoF | protect | External factor: trial equipment problems |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | tic disorder | ARIPIPRAZOLE | targetBased | 4 | Suspended | 01/06/2024 | https://clinicaltrials.gov/study/NCT05361993 | 1 | GoF | protect | External factor: trial equipment problems |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | tic disorder | ARIPIPRAZOLE | targetBased | 4 | Suspended | 01/06/2024 | https://clinicaltrials.gov/study/NCT05361993 | 1 | GoF | protect | External factor: trial equipment problems |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | tic disorder | ARIPIPRAZOLE | targetBased | 4 | Suspended | 01/06/2024 | https://clinicaltrials.gov/study/NCT05361993 | 1 | GoF | protect | External factor: trial equipment problems |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | tic disorder | ARIPIPRAZOLE | targetBased | 4 | Suspended | 01/06/2024 | https://clinicaltrials.gov/study/NCT05361993 | 1 | GoF | protect | External factor: trial equipment problems |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | tic disorder | ARIPIPRAZOLE | targetBased | 4 | Suspended | 01/06/2024 | https://clinicaltrials.gov/study/NCT05361993 | 1 | GoF | protect | External factor: trial equipment problems |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01727700 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2009 | https://clinicaltrials.gov/study/NCT00728312 | 1 | GoF | protect | PI left the VA. |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2009 | https://clinicaltrials.gov/study/NCT00728312 | 1 | GoF | protect | PI left the VA. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2009 | https://clinicaltrials.gov/study/NCT00728312 | 1 | GoF | protect | PI left the VA. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2009 | https://clinicaltrials.gov/study/NCT00728312 | 1 | GoF | protect | PI left the VA. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2009 | https://clinicaltrials.gov/study/NCT00728312 | 1 | GoF | protect | PI left the VA. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Withdrawn | 01/08/2009 | https://clinicaltrials.gov/study/NCT00728312 | 1 | GoF | protect | PI left the VA. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01813656 | 0.5 | GoF | protect | Aripiprazole arm had obvious adverse reactions,especially akathisia. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | ARIPIPRAZOLE | targetBased | 4 | Terminated | 01/09/2012 | https://clinicaltrials.gov/study/NCT01813656 | 0.5 | GoF | protect | Aripiprazole arm had obvious adverse reactions,especially akathisia. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2013 | https://clinicaltrials.gov/study/NCT01727713 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2013 | https://clinicaltrials.gov/study/NCT01727713 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | tic disorder | ARIPIPRAZOLE | targetBased | 4 | Suspended | 01/06/2024 | https://clinicaltrials.gov/study/NCT05361993 | 1 | GoF | protect | External factor: trial equipment problems |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | tic disorder | ARIPIPRAZOLE | targetBased | 4 | Suspended | 01/06/2024 | https://clinicaltrials.gov/study/NCT05361993 | 1 | GoF | protect | External factor: trial equipment problems |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01727700 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01727700 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00095719 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00095719 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00095719 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00095719 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | pervasive developmental disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00870727 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | pervasive developmental disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00870727 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | pervasive developmental disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00870727 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | pervasive developmental disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00870727 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | pervasive developmental disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00870727 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | pervasive developmental disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00870727 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | postpartum depression | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01386086 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | postpartum depression | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01386086 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT01028820 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT01028820 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism spectrum disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT01028820 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism spectrum disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT01028820 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT01028820 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2009 | https://clinicaltrials.gov/study/NCT01028820 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2005 | https://clinicaltrials.gov/study/NCT00221962 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2005 | https://clinicaltrials.gov/study/NCT00221962 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00305370 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00305370 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | tic disorder | ARIPIPRAZOLE | targetBased | 4 | Suspended | 01/06/2024 | https://clinicaltrials.gov/study/NCT05361993 | 1 | LoF | protect | External factor: trial equipment problems |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/01/2013 | https://clinicaltrials.gov/study/NCT01727713 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | tic disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01727700 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ee49f3b1-1650-47ff-9fb1-ea53fe0b92b6 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | pervasive developmental disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00870727 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | pervasive developmental disorder | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00870727 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/02/2011 | https://clinicaltrials.gov/study/NCT01292057 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol dependence | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00082199 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol dependence | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00082199 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00082199 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00082199 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00082199 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00082199 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | postpartum depression | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01386086 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | postpartum depression | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01386086 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | postpartum depression | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01386086 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | postpartum depression | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01386086 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | postpartum depression | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01386086 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | postpartum depression | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01386086 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b40bfd2b-9ff1-45bf-a40f-e9812f1df228 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b6243233-8846-4ea8-a2fa-a563e48fdc29 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffb6ef30-2619-4652-864c-4d5e94526a15 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0424faf3-202f-438a-b65e-2a228790b8f9 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e8fe516e-25fc-45f6-9a88-542deaa1c3e8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ARIPIPRAZOLE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202971s008lbl.pdf | 1 | LoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | conduct disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 17/11/2004 | https://clinicaltrials.gov/study/NCT00250705 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | conduct disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 17/11/2004 | https://clinicaltrials.gov/study/NCT00250705 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1be1bea7-71d5-406a-bcf3-e1d58f406389 | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1be1bea7-71d5-406a-bcf3-e1d58f406389 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1be1bea7-71d5-406a-bcf3-e1d58f406389 | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1be1bea7-71d5-406a-bcf3-e1d58f406389 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1be1bea7-71d5-406a-bcf3-e1d58f406389 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1be1bea7-71d5-406a-bcf3-e1d58f406389 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00305370 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2005 | https://clinicaltrials.gov/study/NCT00221962 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2005 | https://clinicaltrials.gov/study/NCT00221962 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2005 | https://clinicaltrials.gov/study/NCT00221962 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2005 | https://clinicaltrials.gov/study/NCT00221962 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2005 | https://clinicaltrials.gov/study/NCT00221962 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/04/2005 | https://clinicaltrials.gov/study/NCT00221962 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2005 | https://clinicaltrials.gov/study/NCT00208169 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16710a27-aa76-4dd7-92e8-7d3c7efe3e42 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06dda03f-8481-46d6-af02-4f51e1a3a065 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06dda03f-8481-46d6-af02-4f51e1a3a065 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/06/2012 | https://clinicaltrials.gov/study/NCT01710163 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | ARIPIPRAZOLE | targetBased | 4 | Unknown status | 01/06/2012 | https://clinicaltrials.gov/study/NCT01710163 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | social anxiety disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | social anxiety disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | ARIPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f24ce78-525a-4bb1-a23d-03f152558575 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism | ARIPIPRAZOLE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202971s008lbl.pdf | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism | ARIPIPRAZOLE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202971s008lbl.pdf | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism | ARIPIPRAZOLE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202971s008lbl.pdf | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism | ARIPIPRAZOLE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202971s008lbl.pdf | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | ARIPIPRAZOLE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202971s008lbl.pdf | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | ARIPIPRAZOLE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202971s008lbl.pdf | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | treatment resistant depression | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | treatment resistant depression | ARIPIPRAZOLE | targetBased | 4 | Completed | 24/02/2017 | https://clinicaltrials.gov/study/NCT02960763 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Dementia | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Dementia | ARIPIPRAZOLE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Dementia | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00095719 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Dementia | ARIPIPRAZOLE | targetBased | 3 | Completed | 01/12/2003 | https://clinicaltrials.gov/study/NCT00095719 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | social anxiety disorder | ARIPIPRAZOLE | targetBased | 4 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00177008 | 1 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | unipolar depression | AMOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a16297df-3158-48db-85e5-5cd506885556 | 1 | LoF | protect | |||
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | unipolar depression | AMOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=261006c8-3fd0-491b-b322-42beff6f9880 | 1 | LoF | protect | |||
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | unipolar depression | AMOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=261006c8-3fd0-491b-b322-42beff6f9880 | 1 | LoF | protect | |||
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | unipolar depression | AMOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=261006c8-3fd0-491b-b322-42beff6f9880 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | AMOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=261006c8-3fd0-491b-b322-42beff6f9880 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | unipolar depression | AMOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=261006c8-3fd0-491b-b322-42beff6f9880 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | unipolar depression | AMOXAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA17 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | unipolar depression | AMOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a16297df-3158-48db-85e5-5cd506885556 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | unipolar depression | AMOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a16297df-3158-48db-85e5-5cd506885556 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | unipolar depression | AMOXAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a16297df-3158-48db-85e5-5cd506885556 | 1 | LoF | protect | |||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE HYDROCHLORIDE | targetBased | 4 | Completed | 01/08/2006 | https://clinicaltrials.gov/study/NCT00361543 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE HYDROCHLORIDE | targetBased | 4 | Completed | 01/01/2012 | https://clinicaltrials.gov/study/NCT01481883 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE HYDROCHLORIDE | targetBased | 4 | Completed | 17/07/2018 | https://clinicaltrials.gov/study/NCT03418831 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizophrenia | RALOXIFENE HYDROCHLORIDE | targetBased | 4 | Completed | 01/04/2011 | https://clinicaltrials.gov/study/NCT02354001 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizoaffective disorder | RALOXIFENE HYDROCHLORIDE | targetBased | 4 | Completed | 01/04/2011 | https://clinicaltrials.gov/study/NCT02354001 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizoaffective disorder | RALOXIFENE HYDROCHLORIDE | targetBased | 4 | Completed | 01/08/2006 | https://clinicaltrials.gov/study/NCT00361543 | 1 | protect | ||
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | ESR2 | Estrogen receptor beta | schizoaffective disorder | RALOXIFENE HYDROCHLORIDE | targetBased | 4 | Completed | 01/01/2012 | https://clinicaltrials.gov/study/NCT01481883 | 1 | protect | ||
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | unipolar depression | AMINEPTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA19 | 1 | LoF | protect | |||
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | unipolar depression | AMINEPTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA19 | 1 | LoF | protect | |||
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | unipolar depression | AMINEPTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA19 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | AMINEPTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA19 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | AMINEPTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA19 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | AMINEPTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA19 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | AMINEPTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA19 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | AMINEPTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA19 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | AMINEPTINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AA19 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | THIOTHIXENE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17dbfc4c-d62e-4efa-930d-29df7de69fa3 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | THIOTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | THIOTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF04 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | THIOTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | THIOTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF04 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | THIOTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | THIOTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF04 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | THIOTHIXENE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AF04 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | THIOTHIXENE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17dbfc4c-d62e-4efa-930d-29df7de69fa3 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | THIOTHIXENE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17dbfc4c-d62e-4efa-930d-29df7de69fa3 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | THIOTHIXENE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17dbfc4c-d62e-4efa-930d-29df7de69fa3 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | THIOTHIXENE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17dbfc4c-d62e-4efa-930d-29df7de69fa3 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | THIOTHIXENE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17dbfc4c-d62e-4efa-930d-29df7de69fa3 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | THIOTHIXENE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17dbfc4c-d62e-4efa-930d-29df7de69fa3 | 1 | LoF | protect | |||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | delirium | ISOFLURANE | targetBased | 4 | Terminated | 01/01/2014 | https://clinicaltrials.gov/study/NCT02111447 | 1 | protect | Not enough participants | |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | delirium | ISOFLURANE | targetBased | 4 | Terminated | 01/01/2014 | https://clinicaltrials.gov/study/NCT02111447 | 1 | protect | Not enough participants | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | depressive disorder | LEVETIRACETAM | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | alcohol dependence | LEVETIRACETAM | targetBased | 3 | Completed | 01/05/2007 | https://clinicaltrials.gov/study/NCT00758277 | 0.7 | LoF | protect | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | alcohol dependence | LEVETIRACETAM | targetBased | 4 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00325182 | 1 | LoF | protect | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | Tourette syndrome | LEVETIRACETAM | targetBased | 4 | Completed | 01/02/2007 | https://clinicaltrials.gov/study/NCT00370838 | 1 | LoF | protect | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | panic disorder | LEVETIRACETAM | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00279617 | 0.7 | LoF | protect | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | schizophrenia | LEVETIRACETAM | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | alcohol withdrawal | LEVETIRACETAM | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00146471 | 0.7 | LoF | protect | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | Dementia | LEVETIRACETAM | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | anxiety | LEVETIRACETAM | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BLONANSERIN | targetBased | 3 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT01516424 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | BLONANSERIN | targetBased | 3 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT01516424 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | BLONANSERIN | targetBased | 3 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT01516424 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | BLONANSERIN | targetBased | 3 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT01516424 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BLONANSERIN | targetBased | 4 | Terminated | 22/01/2019 | https://clinicaltrials.gov/study/NCT03784222 | 1 | LoF | protect | Company's business decision |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BLONANSERIN | targetBased | 3 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT01516424 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | separation anxiety disorder | VILAZODONE | targetBased | 4 | Completed | 01/12/2013 | https://clinicaltrials.gov/study/NCT01999920 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | separation anxiety disorder | VILAZODONE | targetBased | 4 | Completed | 01/12/2013 | https://clinicaltrials.gov/study/NCT01999920 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VILAZODONE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01715519 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VILAZODONE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01715519 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | VILAZODONE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01715519 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | VILAZODONE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01715519 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VILAZODONE | targetBased | 4 | Completed | 01/12/2011 | https://clinicaltrials.gov/study/NCT01473381 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VILAZODONE | targetBased | 4 | Completed | 01/12/2011 | https://clinicaltrials.gov/study/NCT01473394 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VILAZODONE | targetBased | 4 | Completed | 01/12/2011 | https://clinicaltrials.gov/study/NCT01473394 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VILAZODONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01573598 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VILAZODONE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01573598 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VILAZODONE | targetBased | 4 | Completed | 01/07/2012 | https://clinicaltrials.gov/study/NCT01608295 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VILAZODONE | targetBased | 4 | Completed | 01/07/2012 | https://clinicaltrials.gov/study/NCT01608295 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX24 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX24 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c55ccfb-c4cf-11df-851a-0800200c9a66 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c55ccfb-c4cf-11df-851a-0800200c9a66 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bfef9e19-d0f5-40fa-954c-b73c812eb242 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bfef9e19-d0f5-40fa-954c-b73c812eb242 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VILAZODONE | targetBased | 3 | Completed | 30/06/2012 | https://clinicaltrials.gov/study/NCT01629966 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VILAZODONE | targetBased | 3 | Completed | 30/06/2012 | https://clinicaltrials.gov/study/NCT01629966 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VILAZODONE | targetBased | 3 | Completed | 30/04/2013 | https://clinicaltrials.gov/study/NCT01844115 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VILAZODONE | targetBased | 3 | Completed | 30/04/2013 | https://clinicaltrials.gov/study/NCT01844115 | 0.7 | GoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizoaffective disorder | MODAFINIL | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00423943 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizoaffective disorder | MODAFINIL | targetBased | 4 | Terminated | 01/04/2013 | https://clinicaltrials.gov/study/NCT01913327 | 1 | LoF | protect | Insufficient Funds and Inadequate Subject Recruitment |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | MODAFINIL | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00208715 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | methamphetamine dependence | MODAFINIL | targetBased | 4 | Completed | 01/02/2009 | https://clinicaltrials.gov/study/NCT00751023 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | MODAFINIL | targetBased | 4 | Completed | 01/11/2003 | https://clinicaltrials.gov/study/NCT00086281 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | MODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=01f6690c-1410-42ad-8eb3-e7df32eab3ba | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | MODAFINIL | targetBased | 4 | Terminated | 01/02/2016 | https://clinicaltrials.gov/study/NCT02494102 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | MODAFINIL | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00107809 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | MODAFINIL | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00107848 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | MODAFINIL | targetBased | 4 | Completed | 01/05/2008 | https://clinicaltrials.gov/study/NCT00711464 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | MODAFINIL | targetBased | 4 | Terminated | 01/04/2013 | https://clinicaltrials.gov/study/NCT01913327 | 1 | LoF | protect | Insufficient Funds and Inadequate Subject Recruitment |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | MODAFINIL | targetBased | 4 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00423943 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | MODAFINIL | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00573417 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | MODAFINIL | targetBased | 3 | Withdrawn | 01/12/2018 | https://clinicaltrials.gov/study/NCT04317001 | 0.7 | LoF | protect | Researcher leading the study moved institutions study not feasible |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Sleep Disorder | MODAFINIL | targetBased | 3 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00236080 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | MODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=01f6690c-1410-42ad-8eb3-e7df32eab3ba | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | cocaine dependence | MODAFINIL | targetBased | 3 | Completed | 01/04/2009 | https://clinicaltrials.gov/study/NCT00701532 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar disorder | MODAFINIL | targetBased | 4 | Completed | 01/01/2014 | https://clinicaltrials.gov/study/NCT01965925 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy | MODAFINIL | targetBased | 3 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00066170 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy | MODAFINIL | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00107848 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy | MODAFINIL | targetBased | 3 | Completed | 01/01/2005 | https://clinicaltrials.gov/study/NCT00214968 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy | MODAFINIL | targetBased | 3 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00107796 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | insomnia | MODAFINIL | targetBased | 4 | Completed | 01/01/2005 | https://clinicaltrials.gov/study/NCT00124384 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | MODAFINIL | targetBased | 3 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00228540 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | MODAFINIL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06BA07 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | MODAFINIL | targetBased | 3 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00214981 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | MODAFINIL | targetBased | 3 | Completed | 01/06/2006 | https://clinicaltrials.gov/study/NCT00343811 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | schizophrenia | SAMIDORPHAN | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | schizophrenia | SAMIDORPHAN | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | bipolar I disorder | SAMIDORPHAN | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | bipolar I disorder | SAMIDORPHAN | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | bipolar I disorder | SAMIDORPHAN | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | schizophrenia | SAMIDORPHAN | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | PSILOCYBINE | targetBased | 3 | Not yet recruiting | 01/04/2024 | https://clinicaltrials.gov/study/NCT06247839 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | PSILOCYBINE | targetBased | 3 | Recruiting | 05/03/2024 | https://clinicaltrials.gov/study/NCT06308653 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment resistant depression | PSILOCYBINE | targetBased | 3 | Recruiting | 19/01/2023 | https://clinicaltrials.gov/study/NCT05624268 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment resistant depression | PSILOCYBINE | targetBased | 3 | Recruiting | 14/02/2023 | https://clinicaltrials.gov/study/NCT05711940 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | treatment resistant depression | PSILOCYBINE | targetBased | 3 | Recruiting | 19/04/2024 | https://clinicaltrials.gov/study/NCT06303739 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | PSILOCYBINE | targetBased | 3 | Recruiting | 19/04/2024 | https://clinicaltrials.gov/study/NCT06303739 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | NALUZOTAN | targetBased | 3 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00248183 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | NALUZOTAN | targetBased | 3 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00248183 | 0.7 | GoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | mental or behavioural disorder | SIBUTRAMINE | targetBased | 4 | Completed | 01/04/2001 | https://clinicaltrials.gov/study/NCT00044187 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | SIBUTRAMINE | targetBased | 4 | Completed | 01/04/2001 | https://clinicaltrials.gov/study/NCT00044187 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar disorder | SIBUTRAMINE | targetBased | 4 | Completed | 01/04/2001 | https://clinicaltrials.gov/study/NCT00044187 | 1 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | schizophrenia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00158223 | 1 | LoF | protect | |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00158223 | 1 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00158223 | 1 | LoF | protect | |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00158223 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00158223 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00158223 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00158223 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PIMOZIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AG02 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | Tourette syndrome | PIMOZIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=70b079e2-a1f7-4a93-8685-d60a4d7c1280 | 1 | LoF | protect | |||
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | DRD1 | Dopaminereceptor1 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | DRD1 | Dopamine receptor D1 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | DRD1 | Dopaminereceptor1 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/10/2004 | https://clinicaltrials.gov/study/NCT00158223 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety | PIMOZIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | PIMOZIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | Dementia | NIMODIPINE | targetBased | 4 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00814658 | 1 | LoF | protect | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | depressive disorder | NIMODIPINE | targetBased | 4 | Terminated | 01/08/2008 | https://clinicaltrials.gov/study/NCT00781326 | 1 | LoF | protect | Final cost of study medication was significantly greater than initial estimate, |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN | targetBased | 4 | Completed | 01/10/2017 | https://clinicaltrials.gov/study/NCT03389412 | 1 | GoF | protect | |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN | targetBased | 4 | Unknown status | 01/04/2012 | https://clinicaltrials.gov/study/NCT01582542 | 1 | GoF | protect | |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8ca799f1-7029-4527-9ab4-7512504bb8e2 | 1 | GoF | protect | |||
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN | targetBased | 4 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00209261 | 1 | GoF | protect | |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN | targetBased | 4 | Recruiting | 15/03/2020 | https://clinicaltrials.gov/study/NCT04545931 | 1 | GoF | protect | |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6d55baa9-2b62-469c-93ae-3909ab249332 | 1 | GoF | protect | |||
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN | targetBased | 4 | Completed | 01/04/2011 | https://clinicaltrials.gov/study/NCT01645475 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00134459 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00134459 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245973 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245973 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00134459 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00134459 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00134459 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00134459 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00134459 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00134459 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245973 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245973 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245973 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245973 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245973 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | BIFEPRUNOX | targetBased | 3 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245973 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00230828 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00230828 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Terminated | 01/11/2006 | https://clinicaltrials.gov/study/NCT00366704 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Terminated | 01/11/2006 | https://clinicaltrials.gov/study/NCT00366704 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00193713 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00193713 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Terminated | 01/04/2007 | https://clinicaltrials.gov/study/NCT00396214 | 0.7 | GoF | protect | This trial discontinued on 2 May 2008 due to lack of enrolment |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Terminated | 01/04/2007 | https://clinicaltrials.gov/study/NCT00396214 | 0.7 | GoF | protect | This trial discontinued on 2 May 2008 due to lack of enrolment |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00380224 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00380224 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00193687 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00193687 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00193687 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/09/2005 | https://clinicaltrials.gov/study/NCT00193687 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00366171 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00366171 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00366171 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00366171 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00366171 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BIFEPRUNOX | targetBased | 3 | Completed | 01/11/2006 | https://clinicaltrials.gov/study/NCT00366171 | 0.7 | GoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | attention deficit hyperactivity disorder | NOREPINEPHRINE | targetBased | 4 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT00757029 | 1 | GoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | post-traumatic stress disorder | NOREPINEPHRINE | targetBased | 4 | Active, not recruiting | 01/06/2020 | https://clinicaltrials.gov/study/NCT04597190 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | HYDROCODONE | targetBased | 4 | Completed | 30/01/2018 | https://clinicaltrials.gov/study/NCT03457116 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6ccfbd98-7750-4955-a654-ec104fb666f9 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b3c9e-b7e4-455b-9482-61714aea2b14 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b3c9e-b7e4-455b-9482-61714aea2b14 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=901d4115-f71a-4681-bd0e-c9b691151b78 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=901d4115-f71a-4681-bd0e-c9b691151b78 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=470df63a-5c0f-42df-9023-a330a901153e | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=470df63a-5c0f-42df-9023-a330a901153e | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6ccfbd98-7750-4955-a654-ec104fb666f9 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=901d4115-f71a-4681-bd0e-c9b691151b78 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=470df63a-5c0f-42df-9023-a330a901153e | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9e5daeac-8573-48e9-877f-c08701255c5b | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b3c9e-b7e4-455b-9482-61714aea2b14 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=25f400d9-1d6e-4d38-8f0d-98d471eba73b | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | HYDROCODONE | targetBased | 4 | Completed | 30/01/2018 | https://clinicaltrials.gov/study/NCT03457116 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | HYDROCODONE | targetBased | 4 | Completed | 30/01/2018 | https://clinicaltrials.gov/study/NCT03457116 | 1 | GoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245674 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/10/2018 | https://clinicaltrials.gov/study/NCT03510325 | 1 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/10/2018 | https://clinicaltrials.gov/study/NCT03510325 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00331981 | 1 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00331981 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00436371 | 1 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00436371 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/10/2018 | https://clinicaltrials.gov/study/NCT03510325 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/05/2021 | https://clinicaltrials.gov/study/NCT04446234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT01105481 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2005 | https://clinicaltrials.gov/study/NCT00245674 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01795183 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00331981 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01446328 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01446328 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizophrenia | AMISULPRIDE | targetBased | 4 | Unknown status | 01/10/2017 | https://clinicaltrials.gov/study/NCT03802838 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | schizophrenia | AMISULPRIDE | targetBased | 4 | Unknown status | 01/10/2017 | https://clinicaltrials.gov/study/NCT03802838 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | AMISULPRIDE | targetBased | 4 | Terminated | 01/01/2008 | https://clinicaltrials.gov/study/NCT01615185 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | AMISULPRIDE | targetBased | 4 | Recruiting | 04/05/2021 | https://clinicaltrials.gov/study/NCT04876521 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/05/2021 | https://clinicaltrials.gov/study/NCT04446234 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00761670 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00761670 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00204061 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01246232 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | AMISULPRIDE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01246232 | 1 | LoF | protect | |
Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | HTR5A | 5-hydroxytryptamine receptor 5A | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | HTR1E | 5-hydroxytryptamine receptor 1E | psychosis | AMISULPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL05 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/05/2021 | https://clinicaltrials.gov/study/NCT04446234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/10/2018 | https://clinicaltrials.gov/study/NCT03510325 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/10/2018 | https://clinicaltrials.gov/study/NCT03510325 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/10/2018 | https://clinicaltrials.gov/study/NCT03510325 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/10/2018 | https://clinicaltrials.gov/study/NCT03510325 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/10/2018 | https://clinicaltrials.gov/study/NCT03510325 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | AMISULPRIDE | targetBased | 4 | Not yet recruiting | 01/10/2018 | https://clinicaltrials.gov/study/NCT03510325 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01609153 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | AMISULPRIDE | targetBased | 4 | Completed | 01/05/2011 | https://clinicaltrials.gov/study/NCT01248195 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Dementia | AMISULPRIDE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | anxiety | ESKETAMINE | targetBased | 4 | Recruiting | 30/06/2023 | https://clinicaltrials.gov/study/NCT05925283 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE | targetBased | 4 | Completed | 04/11/2020 | https://clinicaltrials.gov/study/NCT04599855 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE | targetBased | 4 | Recruiting | 08/10/2021 | https://clinicaltrials.gov/study/NCT04303325 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE | targetBased | 3 | Completed | 01/10/2015 | https://clinicaltrials.gov/study/NCT02493868 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/spravato | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE | targetBased | 3 | Completed | 10/08/2015 | https://clinicaltrials.gov/study/NCT02417064 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE | targetBased | 3 | Completed | 20/08/2015 | https://clinicaltrials.gov/study/NCT02422186 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE | targetBased | 3 | Completed | 07/08/2015 | https://clinicaltrials.gov/study/NCT02418585 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE | targetBased | 3 | Withdrawn | 01/12/2019 | https://clinicaltrials.gov/study/NCT03852160 | 0.7 | LoF | protect | New design was developed to better fit company strategy, a new study has replaced 5413541TRD3011 study | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE | targetBased | 3 | Completed | 08/09/2020 | https://clinicaltrials.gov/study/NCT04476446 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | pain agnosia | ESKETAMINE | targetBased | 4 | Recruiting | 08/02/2022 | https://clinicaltrials.gov/study/NCT04964219 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | pain agnosia | ESKETAMINE | targetBased | 4 | Recruiting | 11/08/2022 | https://clinicaltrials.gov/study/NCT05466708 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | unipolar depression | ESKETAMINE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/211243lbl.pdf | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | unipolar depression | ESKETAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06AX27 | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | unipolar depression | ESKETAMINE | targetBased | 4 | Active, not recruiting | 26/04/2021 | https://clinicaltrials.gov/study/NCT04829318 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | treatment resistant depression | ESKETAMINE | targetBased | 4 | Recruiting | 03/06/2024 | https://clinicaltrials.gov/study/NCT06278779 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | postpartum depression | ESKETAMINE | targetBased | 4 | Active, not recruiting | 19/06/2020 | https://clinicaltrials.gov/study/NCT05698394 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | postpartum depression | ESKETAMINE | targetBased | 4 | Recruiting | 01/05/2023 | https://clinicaltrials.gov/study/NCT05826327 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | postpartum depression | ESKETAMINE | targetBased | 4 | Not yet recruiting | 20/02/2022 | https://clinicaltrials.gov/study/NCT05229913 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | ESKETAMINE | targetBased | 4 | Recruiting | 13/10/2022 | https://clinicaltrials.gov/study/NCT05450432 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | ESKETAMINE | targetBased | 3 | Completed | 21/08/2020 | https://clinicaltrials.gov/study/NCT04338321 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | ESKETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d81a6a79-a74a-44b7-822c-0dfa3036eaed | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | ESKETAMINE | targetBased | 4 | Withdrawn | 27/10/2023 | https://clinicaltrials.gov/study/NCT05554627 | 1 | LoF | protect | Study funding was withdrawn by study sponsor (CSR\&D) prior to enrollment due to budget constraints. | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | ESKETAMINE | targetBased | 3 | Completed | 09/06/2017 | https://clinicaltrials.gov/study/NCT03039192 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | ESKETAMINE | targetBased | 3 | Completed | 15/06/2017 | https://clinicaltrials.gov/study/NCT03097133 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | ESKETAMINE | targetBased | 4 | Recruiting | 31/10/2023 | https://clinicaltrials.gov/study/NCT06103760 | 1 | LoF | protect | ||
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | schizophrenia | EXENATIDE | targetBased | 4 | Completed | 01/09/2014 | https://clinicaltrials.gov/study/NCT02417142 | 1 | GoF | protect | |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | schizophrenia | EXENATIDE | targetBased | 4 | Completed | 01/09/2014 | https://clinicaltrials.gov/study/NCT02417142 | 1 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | schizophrenia | EXENATIDE | targetBased | 4 | Completed | 01/09/2014 | https://clinicaltrials.gov/study/NCT02417142 | 1 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | schizoaffective disorder | EXENATIDE | targetBased | 4 | Completed | 01/09/2014 | https://clinicaltrials.gov/study/NCT02417142 | 1 | GoF | protect | |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | schizoaffective disorder | EXENATIDE | targetBased | 4 | Completed | 01/09/2014 | https://clinicaltrials.gov/study/NCT02417142 | 1 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | schizoaffective disorder | EXENATIDE | targetBased | 4 | Completed | 01/09/2014 | https://clinicaltrials.gov/study/NCT02417142 | 1 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | autism spectrum disorder | OXYTOCIN | targetBased | 3 | Completed | 26/07/2018 | https://clinicaltrials.gov/study/NCT03640156 | 0.7 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | autism spectrum disorder | OXYTOCIN | targetBased | 3 | Completed | 09/10/2017 | https://clinicaltrials.gov/study/NCT02985749 | 0.7 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | autism spectrum disorder | OXYTOCIN | targetBased | 4 | Completed | 01/04/2015 | https://clinicaltrials.gov/study/NCT02940574 | 1 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | post-traumatic stress disorder | OXYTOCIN | targetBased | 4 | Completed | 01/08/2011 | https://clinicaltrials.gov/study/NCT01325168 | 1 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | alcohol dependence | OXYTOCIN | targetBased | 3 | Completed | 01/10/2016 | https://clinicaltrials.gov/study/NCT02903251 | 0.7 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | alcohol dependence | OXYTOCIN | targetBased | 4 | Completed | 01/05/2013 | https://clinicaltrials.gov/study/NCT01829516 | 1 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | alcohol dependence | OXYTOCIN | targetBased | 3 | Completed | 01/11/2017 | https://clinicaltrials.gov/study/NCT03339024 | 0.7 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | nicotine dependence | OXYTOCIN | targetBased | 4 | Completed | 01/07/2016 | https://clinicaltrials.gov/study/NCT02595749 | 1 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | schizophrenia | OXYTOCIN | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01614093 | 1 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | schizophrenia | OXYTOCIN | targetBased | 4 | Active, not recruiting | 04/01/2018 | https://clinicaltrials.gov/study/NCT03245437 | 1 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | schizophrenia | OXYTOCIN | targetBased | 3 | Recruiting | 01/03/2012 | https://clinicaltrials.gov/study/NCT01987050 | 0.7 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | drug dependence | OXYTOCIN | targetBased | 4 | Terminated | 01/11/2008 | https://clinicaltrials.gov/study/NCT00975416 | 1 | GoF | protect | |
Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | OXTR | Oxytocin receptor | anxiety | OXYTOCIN | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT01081249 | 1 | GoF | protect | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | depressive disorder | AMLODIPINE | targetBased | 3 | Unknown status | 01/04/2012 | https://clinicaltrials.gov/study/NCT01557153 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | HYDROMORPHONE | targetBased | 3 | Completed | 01/12/2011 | https://clinicaltrials.gov/study/NCT01447212 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | HYDROMORPHONE | targetBased | 3 | Completed | 01/12/2011 | https://clinicaltrials.gov/study/NCT01447212 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=22e635cb-98c0-e4f9-6a71-62d7487a0a6c | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=22e635cb-98c0-e4f9-6a71-62d7487a0a6c | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3832ede8-d3fc-455d-ecab-3b77be5869f5 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3832ede8-d3fc-455d-ecab-3b77be5869f5 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b95bfd6c-cee5-f57d-e053-2995a90a5ce1 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b95bfd6c-cee5-f57d-e053-2995a90a5ce1 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | HYDROMORPHONE | targetBased | 4 | Completed | 20/05/2020 | https://clinicaltrials.gov/study/NCT04396587 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | HYDROMORPHONE | targetBased | 4 | Completed | 20/05/2020 | https://clinicaltrials.gov/study/NCT04396587 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | LEVOMETHADYL ACETATE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BC03 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | LEVOMETHADYL ACETATE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BC03 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | LEVOMETHADYL ACETATE | targetBased | 4 | Completed | 01/03/1995 | https://clinicaltrials.gov/study/NCT00000300 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | LEVOMETHADYL ACETATE | targetBased | 4 | Completed | 01/03/1995 | https://clinicaltrials.gov/study/NCT00000300 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | LEVOMETHADYL ACETATE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/orlaam | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | LEVOMETHADYL ACETATE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/orlaam | 1 | GoF | protect | |||
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | VDR | Vitamin D3 receptor | attention deficit hyperactivity disorder | ERGOCALCIFEROL | targetBased | 4 | Recruiting | 25/02/2021 | https://clinicaltrials.gov/study/NCT04284059 | 1 | GoF | protect | |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | THRB | Thyroid hormone receptor beta | bipolar disorder | LIOTHYRONINE | targetBased | 3 | Completed | 01/07/2008 | https://clinicaltrials.gov/study/NCT00790738 | 0.7 | GoF | protect | |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | THRB | Thyroid hormone receptor beta | bipolar disorder | LIOTHYRONINE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00158990 | 0.7 | GoF | protect | |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | THRB | Thyroid hormone receptor beta | depressive disorder | LIOTHYRONINE | targetBased | 4 | Completed | 01/04/2003 | https://clinicaltrials.gov/study/NCT00531713 | 1 | GoF | protect | |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | THRB | Thyroid hormone receptor beta | depressive disorder | LIOTHYRONINE | targetBased | 4 | Terminated | 01/09/2001 | https://clinicaltrials.gov/study/NCT00296686 | 1 | GoF | protect | Study is no longer funded. |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | THRB | Thyroid hormone receptor beta | depressive disorder | LIOTHYRONINE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00158990 | 0.7 | GoF | protect | |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | THRB | Thyroid hormone receptor beta | depressive disorder | LIOTHYRONINE | targetBased | 4 | Completed | 01/09/1996 | https://clinicaltrials.gov/study/NCT00208702 | 1 | GoF | protect | |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | THRB | Thyroid hormone receptor beta | depressive disorder | LIOTHYRONINE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00021528 | 1 | GoF | protect | |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | THRB | Thyroid hormone receptor beta | depressive disorder | LIOTHYRONINE | targetBased | 3 | Completed | 01/07/2008 | https://clinicaltrials.gov/study/NCT00790738 | 0.7 | GoF | protect | |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | THRB | Thyroid hormone receptor beta | unipolar depression | LIOTHYRONINE | targetBased | 3 | Completed | 01/10/2002 | https://clinicaltrials.gov/study/NCT00158990 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Sleep Disorder | EPLIVANSERIN | targetBased | 3 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00679900 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Sleep Disorder | EPLIVANSERIN | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00253968 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | EPLIVANSERIN | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00308503 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | EPLIVANSERIN | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00253968 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | EPLIVANSERIN | targetBased | 3 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT00805350 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | EPLIVANSERIN | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00253903 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | major depressive disorder | BUPRENORPHINE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01407575 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | major depressive disorder | BUPRENORPHINE | targetBased | 3 | Recruiting | 01/08/2020 | https://clinicaltrials.gov/study/NCT04116528 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | major depressive disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | cocaine dependence | BUPRENORPHINE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00000216 | 0.7 | GoF | protect | ||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | cocaine dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/1995 | https://clinicaltrials.gov/study/NCT00000311 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00007527 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 22/02/2008 | https://clinicaltrials.gov/study/NCT00604188 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00015340 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/03/2013 | https://clinicaltrials.gov/study/NCT03174067 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fc2755a5-3292-4b49-872d-e22c386a4e44 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 24/06/2019 | https://clinicaltrials.gov/study/NCT03604159 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=033f2324-09d4-ce5c-ff60-e3b03d0538c1 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00310934 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00310934 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 4 | Unknown status | 01/08/2008 | https://clinicaltrials.gov/study/NCT00750217 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 4 | Unknown status | 01/08/2008 | https://clinicaltrials.gov/study/NCT00750217 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Terminated | 01/11/2018 | https://clinicaltrials.gov/study/NCT03711318 | 0.7 | GoF | protect | continuing study was no longer feasible |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Terminated | 01/11/2018 | https://clinicaltrials.gov/study/NCT03711318 | 0.7 | GoF | protect | continuing study was no longer feasible |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00367874 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BC01 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BC01 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=36338030-20e2-4ddb-bc06-6c43be4f50a0 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=36338030-20e2-4ddb-bc06-6c43be4f50a0 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00015340 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00015340 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 20/06/2024 | https://clinicaltrials.gov/study/NCT05450718 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 01/12/2023 | https://clinicaltrials.gov/study/NCT05944952 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Completed | 01/03/2023 | https://clinicaltrials.gov/study/NCT05704543 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 04/06/2024 | https://clinicaltrials.gov/study/NCT06323824 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 03/11/2020 | https://clinicaltrials.gov/study/NCT04375033 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Enrolling by invitation | 01/04/2018 | https://clinicaltrials.gov/study/NCT03396276 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Withdrawn | 30/11/2018 | https://clinicaltrials.gov/study/NCT03740243 | 1 | GoF | protect | No enrollment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | BUPRENORPHINE | targetBased | 3 | Recruiting | 01/08/2020 | https://clinicaltrials.gov/study/NCT04116528 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | BUPRENORPHINE | targetBased | 3 | Recruiting | 01/08/2020 | https://clinicaltrials.gov/study/NCT04116528 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | BUPRENORPHINE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01407575 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | major depressive disorder | BUPRENORPHINE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01407575 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/06/2013 | https://clinicaltrials.gov/study/NCT01843023 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BC51 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00367874 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/08/1999 | https://clinicaltrials.gov/study/NCT00015340 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b086772e-d15a-4d13-b1a2-38bfbde1f18c | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=36338030-20e2-4ddb-bc06-6c43be4f50a0 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=593b95a7-b716-cdf4-e053-2a91aa0a35ee | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 4 | Unknown status | 01/08/2008 | https://clinicaltrials.gov/study/NCT00750217 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00000302 | 0.7 | GoF | protect | ||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/04/1996 | https://clinicaltrials.gov/study/NCT00015171 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00310934 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00574067 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | heroin dependence | BUPRENORPHINE | targetBased | 3 | Terminated | 01/11/2018 | https://clinicaltrials.gov/study/NCT03711318 | 0.7 | GoF | protect | continuing study was no longer feasible |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | depressive disorder | BUPRENORPHINE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01407575 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | depressive disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | overdose | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=36338030-20e2-4ddb-bc06-6c43be4f50a0 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | morphine dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | morphine dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | substance withdrawal syndrome | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | substance withdrawal syndrome | BUPRENORPHINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00367874 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | substance withdrawal syndrome | BUPRENORPHINE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/03/2013 | https://clinicaltrials.gov/study/NCT03174067 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fc2755a5-3292-4b49-872d-e22c386a4e44 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fc2755a5-3292-4b49-872d-e22c386a4e44 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00605033 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00605033 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 24/06/2019 | https://clinicaltrials.gov/study/NCT03604159 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE | targetBased | 4 | Completed | 24/06/2019 | https://clinicaltrials.gov/study/NCT03604159 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | BUPRENORPHINE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01407575 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | BUPRENORPHINE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01407575 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | depressive disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 19/10/2020 | https://clinicaltrials.gov/study/NCT04276259 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | overdose | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=36338030-20e2-4ddb-bc06-6c43be4f50a0 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | overdose | BUPRENORPHINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=36338030-20e2-4ddb-bc06-6c43be4f50a0 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | neonatal abstinence syndrome | BUPRENORPHINE | targetBased | 3 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT01452789 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | BUPRENORPHINE | targetBased | 3 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT01452789 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | BUPRENORPHINE | targetBased | 3 | Completed | 01/11/2011 | https://clinicaltrials.gov/study/NCT01452789 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Enrolling by invitation | 01/04/2018 | https://clinicaltrials.gov/study/NCT03396276 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 07/01/2021 | https://clinicaltrials.gov/study/NCT04219540 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Recruiting | 07/01/2021 | https://clinicaltrials.gov/study/NCT04219540 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Completed | 29/08/2019 | https://clinicaltrials.gov/study/NCT03993392 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Completed | 29/08/2019 | https://clinicaltrials.gov/study/NCT03993392 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Completed | 01/11/2020 | https://clinicaltrials.gov/study/NCT04283500 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid use disorder | BUPRENORPHINE | targetBased | 4 | Completed | 01/11/2020 | https://clinicaltrials.gov/study/NCT04283500 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/1995 | https://clinicaltrials.gov/study/NCT00000311 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/1995 | https://clinicaltrials.gov/study/NCT00000311 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | BUPRENORPHINE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00000216 | 0.7 | GoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | cocaine dependence | BUPRENORPHINE | targetBased | 3 | Completed | https://clinicaltrials.gov/study/NCT00000216 | 0.7 | GoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | BUPRENORPHINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00367874 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | BUPRENORPHINE | targetBased | 4 | Completed | 01/02/2003 | https://clinicaltrials.gov/study/NCT00367874 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | BUPRENORPHINE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | substance withdrawal syndrome | BUPRENORPHINE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | morphine dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | morphine dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/01/2001 | https://clinicaltrials.gov/study/NCT00032968 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | morphine dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | morphine dependence | BUPRENORPHINE | targetBased | 3 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00032955 | 0.7 | GoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | ALMOREXANT | targetBased | 3 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00608985 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | ALMOREXANT | targetBased | 3 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00608985 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | PALIPERIDONE | targetBased | 4 | Withdrawn | 01/09/2008 | https://clinicaltrials.gov/study/NCT00766064 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00761579 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/08/2011 | https://clinicaltrials.gov/study/NCT01399450 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/11/2008 | https://clinicaltrials.gov/study/NCT00827840 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE | targetBased | 4 | Unknown status | 01/07/2009 | https://clinicaltrials.gov/study/NCT00937261 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7b8e5b26-b9e4-4704-921b-3c3c0d159916 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE | targetBased | 4 | Terminated | 01/11/2007 | https://clinicaltrials.gov/study/NCT00592358 | 1 | LoF | protect | Slow enrollment. |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE | targetBased | 4 | Terminated | 01/11/2007 | https://clinicaltrials.gov/study/NCT00592358 | 1 | LoF | protect | Slow enrollment. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE | targetBased | 4 | Terminated | 01/11/2007 | https://clinicaltrials.gov/study/NCT00592358 | 1 | LoF | protect | Slow enrollment. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE | targetBased | 4 | Terminated | 01/11/2007 | https://clinicaltrials.gov/study/NCT00592358 | 1 | LoF | protect | Slow enrollment. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE | targetBased | 4 | Terminated | 01/11/2007 | https://clinicaltrials.gov/study/NCT00592358 | 1 | LoF | protect | Slow enrollment. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE | targetBased | 4 | Terminated | 01/11/2007 | https://clinicaltrials.gov/study/NCT00592358 | 1 | LoF | protect | Slow enrollment. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00299715 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | methamphetamine dependence | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01825928 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | methamphetamine dependence | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/12/2006 | https://clinicaltrials.gov/study/NCT00412373 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00535145 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PALIPERIDONE | targetBased | 4 | Withdrawn | 01/09/2008 | https://clinicaltrials.gov/study/NCT00766064 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PALIPERIDONE | targetBased | 4 | Withdrawn | 01/09/2008 | https://clinicaltrials.gov/study/NCT00766064 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PALIPERIDONE | targetBased | 4 | Withdrawn | 01/09/2008 | https://clinicaltrials.gov/study/NCT00766064 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PALIPERIDONE | targetBased | 4 | Withdrawn | 01/09/2008 | https://clinicaltrials.gov/study/NCT00766064 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PALIPERIDONE | targetBased | 4 | Withdrawn | 01/09/2008 | https://clinicaltrials.gov/study/NCT00766064 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | PALIPERIDONE | targetBased | 4 | Withdrawn | 01/09/2008 | https://clinicaltrials.gov/study/NCT00766064 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7b8e5b26-b9e4-4704-921b-3c3c0d159916 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=87d7eb59-2177-431d-bf6b-e14509c0c829 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=87d7eb59-2177-431d-bf6b-e14509c0c829 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=87d7eb59-2177-431d-bf6b-e14509c0c829 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=87d7eb59-2177-431d-bf6b-e14509c0c829 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=87d7eb59-2177-431d-bf6b-e14509c0c829 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=87d7eb59-2177-431d-bf6b-e14509c0c829 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | PALIPERIDONE | targetBased | 4 | Terminated | 01/11/2007 | https://clinicaltrials.gov/study/NCT00592358 | 1 | LoF | protect | Slow enrollment. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00299715 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309686 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00490971 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00535145 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00535145 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00535145 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00535145 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00535145 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00535145 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | PALIPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX13 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2010 | https://clinicaltrials.gov/study/NCT01157585 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/07/2009 | https://clinicaltrials.gov/study/NCT02075528 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=87d7eb59-2177-431d-bf6b-e14509c0c829 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00330863 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00535145 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | Unknown status | 01/04/2015 | https://clinicaltrials.gov/study/NCT02433717 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8de6a6eb-9ed8-4e05-9a4c-d657b5634f76 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2010 | https://clinicaltrials.gov/study/NCT01157585 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PALIPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX13 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | PALIPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX13 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PALIPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX13 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | PALIPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX13 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PALIPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX13 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | PALIPERIDONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX13 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | PALIPERIDONE | targetBased | 3 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00549562 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01825928 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | methamphetamine dependence | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | methamphetamine dependence | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | methamphetamine dependence | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT01822730 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mood disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | PALIPERIDONE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mood disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mood disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mood disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mood disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mood disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mood disorder | PALIPERIDONE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00309699 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00784238 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00784238 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00784238 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00784238 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00784238 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00784238 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism | PALIPERIDONE | targetBased | 3 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00549562 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism | PALIPERIDONE | targetBased | 3 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00549562 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism | PALIPERIDONE | targetBased | 3 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00549562 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism | PALIPERIDONE | targetBased | 3 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00549562 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | PALIPERIDONE | targetBased | 3 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00549562 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | PALIPERIDONE | targetBased | 3 | Completed | 01/11/2007 | https://clinicaltrials.gov/study/NCT00549562 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | DIACETYLMORPHINE | targetBased | 3 | Completed | 01/12/2011 | https://clinicaltrials.gov/study/NCT01447212 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | heroin dependence | DIACETYLMORPHINE | targetBased | 3 | Completed | 01/12/2011 | https://clinicaltrials.gov/study/NCT01447212 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | DIACETYLMORPHINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BC06 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | DIACETYLMORPHINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N07BC06 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | DIACETYLMORPHINE | targetBased | 3 | Completed | 01/03/2002 | https://clinicaltrials.gov/study/NCT00268814 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | DIACETYLMORPHINE | targetBased | 3 | Completed | 01/03/2002 | https://clinicaltrials.gov/study/NCT00268814 | 0.7 | GoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | smoking behavior | BUPROPION HYDROCHLORIDE | targetBased | 3 | Completed | 01/02/2002 | https://clinicaltrials.gov/study/NCT00033592 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar I disorder | BUPROPION HYDROCHLORIDE | targetBased | 3 | Completed | 01/11/2010 | https://clinicaltrials.gov/study/NCT00958633 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7d6bdc28-f334-47f3-8336-c3bebbf57461 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 3 | Completed | 19/01/2006 | https://clinicaltrials.gov/study/NCT00296517 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fddb7191-c4f9-4e82-bd7d-259c3767710a | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06d4d890-11ed-4f31-8778-c73432e3ea69 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION HYDROCHLORIDE | targetBased | 4 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00484692 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION HYDROCHLORIDE | targetBased | 3 | Completed | 01/09/2001 | https://clinicaltrials.gov/study/NCT00086385 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION HYDROCHLORIDE | targetBased | 4 | Completed | 01/07/2009 | https://clinicaltrials.gov/study/NCT00991081 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ef0bb8f2-7710-4236-8b47-57b74c8bca3e | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fddb7191-c4f9-4e82-bd7d-259c3767710a | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06d4d890-11ed-4f31-8778-c73432e3ea69 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=00f9395d-2fe4-4b0c-890a-6873f56fb10a | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a6f7f0e4-87ea-4508-b899-91c8ba819ab7 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=02500709-7f2c-4251-bd8c-94ab6cdadd4c | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00590863 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | mood disorder | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06d4d890-11ed-4f31-8778-c73432e3ea69 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | substance dependence | BUPROPION HYDROCHLORIDE | targetBased | 4 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00484692 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=82f5292b-b113-4f10-9469-04386fa8e9d4 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e9cef726-267e-4e4f-ac12-d92a8664bf20 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b5d286ce-e23f-4dde-b400-cb4832172ece | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ace9755b-e938-4464-beb4-01d6a22eab20 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a93a7bfb-1159-4aa4-8982-9f5347d52ec5 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1de23b24-eb8c-4d16-a929-297132bf00d2 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3b41a8f8-34f4-4a38-9013-9cefafd6009c | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | substance abuse | BUPROPION HYDROCHLORIDE | targetBased | 4 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00484692 | 1 | LoF | protect | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | delirium | MEMANTINE HYDROCHLORIDE | targetBased | 4 | Terminated | 01/03/2006 | https://clinicaltrials.gov/study/NCT00303433 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | attention deficit hyperactivity disorder | MEMANTINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/03/2007 | https://clinicaltrials.gov/study/NCT00586573 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/11/2004 | https://clinicaltrials.gov/study/NCT00768261 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=81496236-0a90-4265-8244-cba6a6b4f3ac | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c65fe60f-8daa-4c77-b072-b3d8540baf38 | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b9f27baf-aa2a-443a-9ef5-e002d23407ba | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2335950c-be3b-4248-ad04-e9763aee47d2 | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1fa2b7bc-94e5-4566-a7c5-419f8fd393a7 | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | MEMANTINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c8f5c20b-4573-44c5-89fc-4da11b2e1fe1 | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | learning disability | MEMANTINE HYDROCHLORIDE | targetBased | 3 | Recruiting | 13/11/2018 | https://clinicaltrials.gov/study/NCT03553875 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | autism spectrum disorder | MEMANTINE HYDROCHLORIDE | targetBased | 3 | Recruiting | 13/11/2018 | https://clinicaltrials.gov/study/NCT03553875 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | autism spectrum disorder | MEMANTINE HYDROCHLORIDE | targetBased | 3 | Completed | 17/02/2015 | https://clinicaltrials.gov/study/NCT01972074 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | autism spectrum disorder | MEMANTINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/01/2010 | https://clinicaltrials.gov/study/NCT01333865 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | autism | MEMANTINE HYDROCHLORIDE | targetBased | 3 | Recruiting | 13/11/2018 | https://clinicaltrials.gov/study/NCT03553875 | 0.7 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MEPERIDINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fae5cc34-5917-4445-9516-25f97ffca8db | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MEPERIDINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fae5cc34-5917-4445-9516-25f97ffca8db | 1 | GoF | protect | |||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar I disorder | KETAMINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/06/2017 | https://clinicaltrials.gov/study/NCT03156504 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | opioid dependence | KETAMINE HYDROCHLORIDE | targetBased | 3 | Active, not recruiting | 25/11/2017 | https://clinicaltrials.gov/study/NCT03345173 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE HYDROCHLORIDE | targetBased | 4 | Unknown status | 01/12/2018 | https://clinicaltrials.gov/study/NCT03666494 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/09/2021 | https://clinicaltrials.gov/study/NCT05026203 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | KETAMINE HYDROCHLORIDE | targetBased | 4 | Completed | 02/05/2017 | https://clinicaltrials.gov/study/NCT03194594 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | unipolar depression | KETAMINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/06/2017 | https://clinicaltrials.gov/study/NCT03156504 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | KETAMINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/06/2017 | https://clinicaltrials.gov/study/NCT03156504 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | KETAMINE HYDROCHLORIDE | targetBased | 3 | Withdrawn | 01/08/2019 | https://clinicaltrials.gov/study/NCT03051945 | 0.7 | LoF | protect | Unable to perform brain imaging | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | KETAMINE HYDROCHLORIDE | targetBased | 4 | Not yet recruiting | 01/01/2023 | https://clinicaltrials.gov/study/NCT05506462 | 1 | LoF | protect | ||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALOXONE HYDROCHLORIDE | targetBased | 4 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT02038790 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | NALOXONE HYDROCHLORIDE | targetBased | 4 | Withdrawn | 01/06/2023 | https://clinicaltrials.gov/study/NCT05808881 | 1 | LoF | protect | Due to changes in research objectives and methodological approach. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=236349ef-2cb5-47ca-a3a5-99534c3a4996 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=236349ef-2cb5-47ca-a3a5-99534c3a4996 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9be31bdf-e220-2978-e053-2a95a90a03c6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9be31bdf-e220-2978-e053-2a95a90a03c6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=784a0e98-c2d6-f845-e053-2991aa0ac4b4 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | unipolar depression | NALOXONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=784a0e98-c2d6-f845-e053-2991aa0ac4b4 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE HYDROCHLORIDE | targetBased | 4 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT02038790 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE HYDROCHLORIDE | targetBased | 4 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT02038790 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE HYDROCHLORIDE | targetBased | 4 | Withdrawn | 01/06/2023 | https://clinicaltrials.gov/study/NCT05808881 | 1 | LoF | protect | Due to changes in research objectives and methodological approach. |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXONE HYDROCHLORIDE | targetBased | 4 | Withdrawn | 01/06/2023 | https://clinicaltrials.gov/study/NCT05808881 | 1 | LoF | protect | Due to changes in research objectives and methodological approach. |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | unipolar depression | NALOXONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9be31bdf-e220-2978-e053-2a95a90a03c6 | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | unipolar depression | NALOXONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=784a0e98-c2d6-f845-e053-2991aa0ac4b4 | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | unipolar depression | NALOXONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=236349ef-2cb5-47ca-a3a5-99534c3a4996 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obsessive-compulsive disorder | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | Completed | 01/10/2013 | https://clinicaltrials.gov/study/NCT02194075 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 3 | Terminated | 01/04/2002 | https://clinicaltrials.gov/study/NCT00031798 | 0.7 | LoF | protect | low accrual; loss of funding |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 3 | Completed | 01/11/2005 | https://clinicaltrials.gov/study/NCT00253747 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | Completed | 19/09/2019 | https://clinicaltrials.gov/study/NCT04152629 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT01065259 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2bfb390f-ba99-4d21-8a9e-50fa8ec217c0 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | Withdrawn | 31/10/2018 | https://clinicaltrials.gov/study/NCT03580005 | 1 | LoF | protect | The study was cancelled prior to the enrollment of any participants. |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00564954 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=effd952d-ac94-47bb-b107-589a4934dcca | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHYLPHENIDATE HYDROCHLORIDE | targetBased | 4 | Completed | 30/07/2016 | https://clinicaltrials.gov/study/NCT02470234 | 1 | LoF | protect | |
Thrombin 1536 HTS | F2_modulation | F2 | Prothrombin | Dementia | DABIGATRAN ETEXILATE | targetBased | 4 | Completed | 03/04/2017 | https://clinicaltrials.gov/study/NCT03061006 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | major depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 15/03/2017 | https://clinicaltrials.gov/study/NCT03131050 | 1 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | major depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 15/03/2017 | https://clinicaltrials.gov/study/NCT03131050 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | major depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 15/03/2017 | https://clinicaltrials.gov/study/NCT03131050 | 1 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | major depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 15/03/2017 | https://clinicaltrials.gov/study/NCT03131050 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | major depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 15/03/2017 | https://clinicaltrials.gov/study/NCT03131050 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 01/01/2018 | https://clinicaltrials.gov/study/NCT03386448 | 1 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 01/01/2018 | https://clinicaltrials.gov/study/NCT03386448 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 01/01/2018 | https://clinicaltrials.gov/study/NCT03386448 | 1 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 01/01/2018 | https://clinicaltrials.gov/study/NCT03386448 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | depressive disorder | SCOPOLAMINE | targetBased | 4 | Completed | 01/01/2018 | https://clinicaltrials.gov/study/NCT03386448 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Dementia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Dementia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Dementia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | LEVOMEPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA02 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | LEVOMEPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA02 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | LEVOMEPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | LEVOMEPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | LEVOMEPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | LEVOMEPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA02 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | LEVOMEPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | LEVOMEPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA02 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | LEVOMEPROMAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AA02 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety | LEVOMEPROMAZINE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | SUVOREXANT | targetBased | 4 | Recruiting | 18/04/2019 | https://clinicaltrials.gov/study/NCT03768713 | 1 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | SUVOREXANT | targetBased | 4 | Completed | 25/05/2017 | https://clinicaltrials.gov/study/NCT03034018 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | SUVOREXANT | targetBased | 4 | Completed | 25/05/2017 | https://clinicaltrials.gov/study/NCT03034018 | 1 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | SUVOREXANT | targetBased | 4 | Completed | 15/04/2018 | https://clinicaltrials.gov/study/NCT03312517 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | SUVOREXANT | targetBased | 4 | Completed | 15/04/2018 | https://clinicaltrials.gov/study/NCT03312517 | 1 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | SUVOREXANT | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e5b72731-1acb-45b7-9c13-290ad12d3951 | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | SUVOREXANT | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e5b72731-1acb-45b7-9c13-290ad12d3951 | 1 | LoF | protect | |||
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | panic disorder | SUVOREXANT | targetBased | 4 | Completed | 01/05/2016 | https://clinicaltrials.gov/study/NCT02593682 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | panic disorder | SUVOREXANT | targetBased | 4 | Completed | 01/05/2016 | https://clinicaltrials.gov/study/NCT02593682 | 1 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | post-traumatic stress disorder | SUVOREXANT | targetBased | 4 | Completed | 03/01/2017 | https://clinicaltrials.gov/study/NCT02849548 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | post-traumatic stress disorder | SUVOREXANT | targetBased | 4 | Completed | 03/01/2017 | https://clinicaltrials.gov/study/NCT02849548 | 1 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | Sleep Disorder | SUVOREXANT | targetBased | 4 | Completed | 01/02/2016 | https://clinicaltrials.gov/study/NCT02491788 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | Sleep Disorder | SUVOREXANT | targetBased | 4 | Completed | 01/02/2016 | https://clinicaltrials.gov/study/NCT02491788 | 1 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | delirium | SUVOREXANT | targetBased | 3 | Completed | 22/10/2020 | https://clinicaltrials.gov/study/NCT04571944 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | delirium | SUVOREXANT | targetBased | 3 | Completed | 22/10/2020 | https://clinicaltrials.gov/study/NCT04571944 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHYLNALTREXONE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/relistor | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHYLNALTREXONE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/relistor | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE ASPARTATE | targetBased | 3 | Completed | 25/04/2005 | https://clinicaltrials.gov/study/NCT00152022 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE ASPARTATE | targetBased | 3 | Completed | 10/03/2005 | https://clinicaltrials.gov/study/NCT00152035 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | AMPHETAMINE ASPARTATE | targetBased | 3 | Completed | 27/01/2005 | https://clinicaltrials.gov/study/NCT00150579 | 0.7 | protect | ||
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE MESYLATE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE MESYLATE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE MESYLATE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE MESYLATE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE MESYLATE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19a92a99-f73a-42f5-b048-28ba0b4df9e6 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19a92a99-f73a-42f5-b048-28ba0b4df9e6 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d0fea556-a015-45c9-98ef-a8b17da4c889 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aca8b358-d172-43d6-95bb-8064b8ed680c | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aca8b358-d172-43d6-95bb-8064b8ed680c | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ed60a885-6b02-48c8-979f-27d371e91d6e | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ed60a885-6b02-48c8-979f-27d371e91d6e | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=547d2a83-fa9e-44e9-9538-fe7f9be92ebb | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=547d2a83-fa9e-44e9-9538-fe7f9be92ebb | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00178971 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizoaffective disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00178971 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BUSPIRONE HYDROCHLORIDE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00178971 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BUSPIRONE HYDROCHLORIDE | targetBased | 3 | Completed | 01/01/2003 | https://clinicaltrials.gov/study/NCT00178971 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19a92a99-f73a-42f5-b048-28ba0b4df9e6 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | BUSPIRONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19a92a99-f73a-42f5-b048-28ba0b4df9e6 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | MOLINDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | MOLINDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1275e92f-9573-4d0c-8e77-1c9ac47696d2 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | NEFAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0bd4c34a-4f43-4c84-8b98-1d074cba97d5 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | NEFAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0bd4c34a-4f43-4c84-8b98-1d074cba97d5 | 1 | LoF | protect | |||
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN ACETATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6d55baa9-2b62-469c-93ae-3909ab249332 | 1 | GoF | protect | |||
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN ACETATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d9d8442a-4722-4b41-9faa-1ee853a4cc3b | 1 | GoF | protect | |||
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN ACETATE | targetBased | 4 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00209261 | 1 | GoF | protect | |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN ACETATE | targetBased | 3 | Completed | 01/07/2013 | https://clinicaltrials.gov/study/NCT02538302 | 0.7 | GoF | protect | |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN ACETATE | targetBased | 4 | Recruiting | 15/03/2020 | https://clinicaltrials.gov/study/NCT04545931 | 1 | GoF | protect | |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | enuresis | DESMOPRESSIN ACETATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8ca799f1-7029-4527-9ab4-7512504bb8e2 | 1 | GoF | protect | |||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | drug dependence | SEVOFLURANE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02334046 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | delirium | SEVOFLURANE | targetBased | 4 | Withdrawn | 01/09/2017 | https://clinicaltrials.gov/study/NCT02394418 | 1 | protect | for technical reasons | |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | delirium | SEVOFLURANE | targetBased | 4 | Recruiting | 21/03/2022 | https://clinicaltrials.gov/study/NCT05158998 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | delirium | SEVOFLURANE | targetBased | 4 | Not yet recruiting | 01/02/2024 | https://clinicaltrials.gov/study/NCT06214117 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | delirium | SEVOFLURANE | targetBased | 4 | Completed | 01/05/2022 | https://clinicaltrials.gov/study/NCT05331027 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | delirium | SEVOFLURANE | targetBased | 4 | Terminated | 01/01/2014 | https://clinicaltrials.gov/study/NCT02111447 | 1 | protect | Not enough participants | |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | depressive disorder | SEVOFLURANE | targetBased | 4 | Unknown status | 01/07/2014 | https://clinicaltrials.gov/study/NCT02267980 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | depressive disorder | SEVOFLURANE | targetBased | 4 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT01870219 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | depressive disorder | SEVOFLURANE | targetBased | 4 | Completed | 01/02/2012 | https://clinicaltrials.gov/study/NCT01870219 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | depressive disorder | SEVOFLURANE | targetBased | 4 | Unknown status | 01/07/2014 | https://clinicaltrials.gov/study/NCT02267980 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | delirium | SEVOFLURANE | targetBased | 4 | Withdrawn | 01/09/2017 | https://clinicaltrials.gov/study/NCT02394418 | 1 | protect | for technical reasons | |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | delirium | SEVOFLURANE | targetBased | 4 | Not yet recruiting | 01/02/2024 | https://clinicaltrials.gov/study/NCT06214117 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | delirium | SEVOFLURANE | targetBased | 4 | Terminated | 01/01/2014 | https://clinicaltrials.gov/study/NCT02111447 | 1 | protect | Not enough participants | |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | delirium | SEVOFLURANE | targetBased | 4 | Completed | 01/05/2022 | https://clinicaltrials.gov/study/NCT05331027 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | delirium | SEVOFLURANE | targetBased | 4 | Recruiting | 21/03/2022 | https://clinicaltrials.gov/study/NCT05158998 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | Agitation | SEVOFLURANE | targetBased | 4 | Not yet recruiting | 15/11/2022 | https://clinicaltrials.gov/study/NCT05624424 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | Agitation | SEVOFLURANE | targetBased | 4 | Completed | 30/01/2022 | https://clinicaltrials.gov/study/NCT05223010 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | Agitation | SEVOFLURANE | targetBased | 4 | Unknown status | 01/05/2014 | https://clinicaltrials.gov/study/NCT02169843 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | Agitation | SEVOFLURANE | targetBased | 4 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02428283 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | Agitation | SEVOFLURANE | targetBased | 4 | Completed | 01/04/2013 | https://clinicaltrials.gov/study/NCT01878656 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | drug dependence | SEVOFLURANE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02334046 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | Agitation | SEVOFLURANE | targetBased | 4 | Completed | 30/01/2022 | https://clinicaltrials.gov/study/NCT05223010 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | Agitation | SEVOFLURANE | targetBased | 4 | Not yet recruiting | 15/11/2022 | https://clinicaltrials.gov/study/NCT05624424 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | Agitation | SEVOFLURANE | targetBased | 4 | Unknown status | 01/05/2014 | https://clinicaltrials.gov/study/NCT02169843 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | Agitation | SEVOFLURANE | targetBased | 4 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02428283 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | Agitation | SEVOFLURANE | targetBased | 4 | Completed | 01/04/2013 | https://clinicaltrials.gov/study/NCT01878656 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | delirium | DESFLURANE | targetBased | 4 | Completed | 01/05/2022 | https://clinicaltrials.gov/study/NCT05331027 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | delirium | DESFLURANE | targetBased | 4 | Completed | 01/05/2022 | https://clinicaltrials.gov/study/NCT05331027 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | KCNK3 | Potassium channel subfamily K member 3 | Agitation | DESFLURANE | targetBased | 4 | Completed | 01/04/2013 | https://clinicaltrials.gov/study/NCT01878656 | 1 | protect | ||
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | KCNK9 | two-pore domain potassium channel | Agitation | DESFLURANE | targetBased | 4 | Completed | 01/04/2013 | https://clinicaltrials.gov/study/NCT01878656 | 1 | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17b3356e-458d-47f6-89a5-80828ab48d4c | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE HYDROCHLORIDE | targetBased | 3 | Completed | 01/06/2007 | https://clinicaltrials.gov/study/NCT00775203 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=66da652a-72b4-c17f-e053-2a91aa0a8d69 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | TRAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=10a30879-f6e2-4030-95b8-0979c18c418a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | TRAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=49196e9e-aeef-4663-8be9-6b523ae7fb7a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4a44bde6-c348-4316-b0e0-c24b407cb823 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4a44bde6-c348-4316-b0e0-c24b407cb823 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c796a39-d87f-4358-9d4b-26e27464b642 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c796a39-d87f-4358-9d4b-26e27464b642 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06cc3fba-68f9-4188-a239-fbd37a9f563a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=06cc3fba-68f9-4188-a239-fbd37a9f563a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c796a39-d87f-4358-9d4b-26e27464b642 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c796a39-d87f-4358-9d4b-26e27464b642 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5e70e915-b946-4a80-bcc6-3f49bc30f2f5 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHADONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5e70e915-b946-4a80-bcc6-3f49bc30f2f5 | 1 | GoF | protect | |||
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | anxiety | LITHIUM CARBONATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | alcohol dependence | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | insomnia | LITHIUM CARBONATE | targetBased | 4 | Completed | 06/11/2020 | https://clinicaltrials.gov/study/NCT04479566 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | conduct disorder | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00000385 | 0.7 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | schizophrenia | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00183443 | 0.7 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | schizophrenia | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00202306 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | schizophrenia | LITHIUM CARBONATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01588457 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7dc9c6d2-6d9a-49e4-a8ab-437b0ed5f84e | 1 | LoF | protect | |||
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=04518b80-7563-4544-bf05-04f286223faa | 1 | LoF | protect | |||
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00976794 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/06/2012 | https://clinicaltrials.gov/study/NCT01710163 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | Withdrawn | 01/09/2011 | https://clinicaltrials.gov/study/NCT01495156 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=05312159-3d8a-45e0-99cb-b83a7b200cd3 | 1 | LoF | protect | |||
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | aggressive behavior | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00000385 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | schizophrenia | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00202306 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | schizophrenia | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/02/2005 | https://clinicaltrials.gov/study/NCT00183443 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | schizophrenia | LITHIUM CARBONATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/06/2009 | https://clinicaltrials.gov/study/NCT00927550 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00021528 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/09/2009 | https://clinicaltrials.gov/study/NCT00974155 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/08/2017 | https://clinicaltrials.gov/study/NCT03219008 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/01/2010 | https://clinicaltrials.gov/study/NCT01028508 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/12/2007 | https://clinicaltrials.gov/study/NCT00602537 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | anxiety | LITHIUM CARBONATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | treatment resistant depression | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/11/2008 | https://clinicaltrials.gov/study/NCT00789854 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | unipolar depression | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=42bed965-4b8f-4471-bcc9-091f87238653 | 1 | LoF | protect | |||
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | major depressive disorder | LITHIUM CARBONATE | targetBased | 3 | Terminated | 01/06/2007 | https://clinicaltrials.gov/study/NCT00400088 | 0.7 | LoF | protect | Recruitment difficulties |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | major depressive disorder | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/11/2008 | https://clinicaltrials.gov/study/NCT00789854 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | major depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT00627887 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | major depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01416220 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | major depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Terminated | 01/05/2009 | https://clinicaltrials.gov/study/NCT00926835 | 1 | LoF | protect | due to patient recruitment difficulties |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/05/2010 | https://clinicaltrials.gov/study/NCT02901249 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/11/2016 | https://clinicaltrials.gov/study/NCT03004521 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00044616 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Terminated | 01/07/2009 | https://clinicaltrials.gov/study/NCT01305707 | 1 | LoF | protect | Difficulties in recruiting |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00021528 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/08/2017 | https://clinicaltrials.gov/study/NCT03219008 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/09/2009 | https://clinicaltrials.gov/study/NCT00974155 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | autism spectrum disorder | LITHIUM CARBONATE | targetBased | 3 | Active, not recruiting | 21/02/2022 | https://clinicaltrials.gov/study/NCT04623398 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | alcohol dependence | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/11/2001 | https://clinicaltrials.gov/study/NCT00202306 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7f3aa4f5-908a-44e7-8113-b64f91dc86e7 | 1 | LoF | protect | |||
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Withdrawn | 01/12/2006 | https://clinicaltrials.gov/study/NCT01075126 | 1 | LoF | protect | key investigator relocated. |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/06/2012 | https://clinicaltrials.gov/study/NCT01938859 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e038fdbc-6d80-4840-afb6-032bf006913f | 1 | LoF | protect | |||
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01588457 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/03/1996 | https://clinicaltrials.gov/study/NCT00870311 | 1 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | aggressive behavior | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00000385 | 0.7 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | insomnia | LITHIUM CARBONATE | targetBased | 4 | Completed | 06/11/2020 | https://clinicaltrials.gov/study/NCT04479566 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | major depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01416220 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | major depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Terminated | 01/05/2009 | https://clinicaltrials.gov/study/NCT00926835 | 1 | LoF | protect | due to patient recruitment difficulties |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | major depressive disorder | LITHIUM CARBONATE | targetBased | 3 | Terminated | 01/06/2007 | https://clinicaltrials.gov/study/NCT00400088 | 0.7 | LoF | protect | Recruitment difficulties |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | major depressive disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/01/2008 | https://clinicaltrials.gov/study/NCT00627887 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | major depressive disorder | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/11/2008 | https://clinicaltrials.gov/study/NCT00789854 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | Dementia | LITHIUM CARBONATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | unipolar depression | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=42bed965-4b8f-4471-bcc9-091f87238653 | 1 | LoF | protect | |||
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | treatment resistant depression | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/11/2008 | https://clinicaltrials.gov/study/NCT00789854 | 0.7 | LoF | protect | |
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | autism spectrum disorder | LITHIUM CARBONATE | targetBased | 3 | Active, not recruiting | 21/02/2022 | https://clinicaltrials.gov/study/NCT04623398 | 0.7 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | Dementia | LITHIUM CARBONATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=05312159-3d8a-45e0-99cb-b83a7b200cd3 | 1 | LoF | protect | |||
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/04/2007 | https://clinicaltrials.gov/study/NCT00608075 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7dc9c6d2-6d9a-49e4-a8ab-437b0ed5f84e | 1 | LoF | protect | |||
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | Withdrawn | 01/09/2011 | https://clinicaltrials.gov/study/NCT01495156 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01588457 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/06/2012 | https://clinicaltrials.gov/study/NCT01710163 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar I disorder | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=04518b80-7563-4544-bf05-04f286223faa | 1 | LoF | protect | |||
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Terminated | 28/03/2017 | https://clinicaltrials.gov/study/NCT03210480 | 1 | LoF | protect | Sponsor's decision due to slow enrollment rate. |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Terminated | 01/01/2012 | https://clinicaltrials.gov/study/NCT01526148 | 1 | LoF | protect | Ran out of funding |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/07/2001 | https://clinicaltrials.gov/study/NCT00177567 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/09/2013 | https://clinicaltrials.gov/study/NCT01893229 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Unknown status | 01/06/2017 | https://clinicaltrials.gov/study/NCT03148535 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03685ed5-d626-472a-b268-fcb8259f5b41 | 1 | LoF | protect | |||
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar disorder | LITHIUM CARBONATE | targetBased | 4 | Completed | 01/02/2001 | https://clinicaltrials.gov/study/NCT00044616 | 1 | LoF | protect | |
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | conduct disorder | LITHIUM CARBONATE | targetBased | 3 | Completed | 01/09/1997 | https://clinicaltrials.gov/study/NCT00000385 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE DECANOATE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE DECANOATE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE DECANOATE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE DECANOATE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE DECANOATE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE DECANOATE | targetBased | 4 | Completed | 01/12/2000 | https://clinicaltrials.gov/study/NCT00014001 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | OXYCODONE HYDROCHLORIDE | targetBased | 4 | Not yet recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT06444997 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | OXYCODONE HYDROCHLORIDE | targetBased | 4 | Not yet recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT06444997 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c9ff0d-46e8-448c-944a-7ad59d1afd6d | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c9ff0d-46e8-448c-944a-7ad59d1afd6d | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=504aa63a-4772-2e03-e054-00144ff88e88 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=504aa63a-4772-2e03-e054-00144ff88e88 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3848642e-cc9e-4150-8199-281b294c18bc | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | OXYCODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3848642e-cc9e-4150-8199-281b294c18bc | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | Terminated | 17/05/2021 | https://clinicaltrials.gov/study/NCT04766996 | 1 | LoF | protect | Loss of surgery team member deemed the study procedures impossible to achieve, and no replacement could be found in a timely manner to complete trial as initially planned. |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | Terminated | 17/05/2021 | https://clinicaltrials.gov/study/NCT04766996 | 1 | LoF | protect | Loss of surgery team member deemed the study procedures impossible to achieve, and no replacement could be found in a timely manner to complete trial as initially planned. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | Terminated | 17/05/2021 | https://clinicaltrials.gov/study/NCT04766996 | 1 | LoF | protect | Loss of surgery team member deemed the study procedures impossible to achieve, and no replacement could be found in a timely manner to complete trial as initially planned. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | Terminated | 17/05/2021 | https://clinicaltrials.gov/study/NCT04766996 | 1 | LoF | protect | Loss of surgery team member deemed the study procedures impossible to achieve, and no replacement could be found in a timely manner to complete trial as initially planned. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | Terminated | 17/05/2021 | https://clinicaltrials.gov/study/NCT04766996 | 1 | LoF | protect | Loss of surgery team member deemed the study procedures impossible to achieve, and no replacement could be found in a timely manner to complete trial as initially planned. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | opioid dependence | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | Terminated | 17/05/2021 | https://clinicaltrials.gov/study/NCT04766996 | 1 | LoF | protect | Loss of surgery team member deemed the study procedures impossible to achieve, and no replacement could be found in a timely manner to complete trial as initially planned. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Anorexia | METOCLOPRAMIDE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=80fb18a3-824a-4360-947e-63f0a167245b | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE ENANTHATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02307396 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | FLUPHENAZINE ENANTHATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | methamphetamine dependence | METHAMPHETAMINE HYDROCHLORIDE | targetBased | 4 | Completed | 16/08/2019 | https://clinicaltrials.gov/study/NCT03973489 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHAMPHETAMINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f03a68d5-ed00-8a2d-af68-28be909ea85f | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=af0159a8-dff5-449a-aa2b-a0c430081e21 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00947375 | 1 | LoF | protect | All of the mentioned aim and objectives were achieved before the February 2007 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1a0e38cb-fd9f-4962-9f81-5c0023ca6b4c | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 3 | Completed | 05/11/2019 | https://clinicaltrials.gov/study/NCT04327843 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | delirium | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01174290 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00947375 | 1 | LoF | protect | All of the mentioned aim and objectives were achieved before the February 2007 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1a0e38cb-fd9f-4962-9f81-5c0023ca6b4c | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1a0e38cb-fd9f-4962-9f81-5c0023ca6b4c | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1a0e38cb-fd9f-4962-9f81-5c0023ca6b4c | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00947375 | 1 | LoF | protect | All of the mentioned aim and objectives were achieved before the February 2007 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00947375 | 1 | LoF | protect | All of the mentioned aim and objectives were achieved before the February 2007 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00947375 | 1 | LoF | protect | All of the mentioned aim and objectives were achieved before the February 2007 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00947375 | 1 | LoF | protect | All of the mentioned aim and objectives were achieved before the February 2007 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00947375 | 1 | LoF | protect | All of the mentioned aim and objectives were achieved before the February 2007 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL DECANOATE | targetBased | 4 | Terminated | 01/01/2005 | https://clinicaltrials.gov/study/NCT00947375 | 1 | LoF | protect | All of the mentioned aim and objectives were achieved before the February 2007 |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL DECANOATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=df9801fc-03fe-41da-a6b3-0f76788217c9 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=73828e5b-6a29-21d9-e053-2991aa0acac4 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=73828e5b-6a29-21d9-e053-2991aa0acac4 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=48a7e42b-934f-4ec6-e054-00144ff88e88 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=48a7e42b-934f-4ec6-e054-00144ff88e88 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=44aeca03-3ac2-4d5b-91c2-9d0442086468 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=44aeca03-3ac2-4d5b-91c2-9d0442086468 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=df9801fc-03fe-41da-a6b3-0f76788217c9 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=44aeca03-3ac2-4d5b-91c2-9d0442086468 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1cab3106-1064-4b42-892b-39f405d9e02f | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=73828e5b-6a29-21d9-e053-2991aa0acac4 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=160cd55a-a8ed-43f2-baf7-046d3c3b317f | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE PHOSPHATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=48a7e42b-934f-4ec6-e054-00144ff88e88 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | NALBUPHINE HYDROCHLORIDE | targetBased | 4 | Recruiting | 01/03/2022 | https://clinicaltrials.gov/study/NCT05273671 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Agitation | NALBUPHINE HYDROCHLORIDE | targetBased | 4 | Recruiting | 01/03/2022 | https://clinicaltrials.gov/study/NCT05273671 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | NALBUPHINE HYDROCHLORIDE | targetBased | 3 | Not yet recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06306040 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | delirium | NALBUPHINE HYDROCHLORIDE | targetBased | 3 | Not yet recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06306040 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | Agitation | NALBUPHINE HYDROCHLORIDE | targetBased | 4 | Recruiting | 01/03/2022 | https://clinicaltrials.gov/study/NCT05273671 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | delirium | NALBUPHINE HYDROCHLORIDE | targetBased | 3 | Not yet recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06306040 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Self-injurious behavior | NALTREXONE HYDROCHLORIDE | targetBased | 3 | Unknown status | 01/07/1997 | https://clinicaltrials.gov/study/NCT00065936 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | Self-injurious behavior | NALTREXONE HYDROCHLORIDE | targetBased | 3 | Unknown status | 01/07/1997 | https://clinicaltrials.gov/study/NCT00065936 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | Self-injurious behavior | NALTREXONE HYDROCHLORIDE | targetBased | 3 | Unknown status | 01/07/1997 | https://clinicaltrials.gov/study/NCT00065936 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LOXAPINE SUCCINATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=dee2537b-1bd8-42f6-990f-62359e646822 | 1 | LoF | protect | |||
Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | GSK3A | Glycogen synthase kinase-3 alpha | bipolar I disorder | LITHIUM CITRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1a04cc23-61fa-455b-9718-2cdcf54036e0 | 1 | LoF | protect | |||
qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | IMPA1 | Inositol monophosphatase 1 | bipolar I disorder | LITHIUM CITRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1a04cc23-61fa-455b-9718-2cdcf54036e0 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | binge eating | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=704e4378-ca83-445c-8b45-3cfa51c1ecad | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | Completed | 01/04/2013 | https://clinicaltrials.gov/study/NCT01863459 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Terminated | 01/11/2012 | https://clinicaltrials.gov/study/NCT01738698 | 0.7 | protect | Study was discontinued due to non-safety related business prioritization decisions. No subjects were randomized. | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Terminated | 01/02/2013 | https://clinicaltrials.gov/study/NCT01760889 | 0.7 | protect | Study was discontinued due to non-safety related business prioritization decisions. No subjects were randomized | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Terminated | 01/02/2013 | https://clinicaltrials.gov/study/NCT01760993 | 0.7 | protect | Study was discontinued due to non-safety related business prioritization decisions. No subjects were randomized. | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Withdrawn | 27/01/2012 | https://clinicaltrials.gov/study/NCT01234298 | 0.7 | protect | Study was discontinued due to non-safety related business prioritization decisions | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Completed | 27/10/2011 | https://clinicaltrials.gov/study/NCT01436149 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Terminated | 27/02/2012 | https://clinicaltrials.gov/study/NCT01436175 | 0.35 | protect | SPD489 failed to demonstrate a benefit as adjunctive treatment to antidepressants. Termination was not related to any new safety findings. | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01148979 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Completed | 19/10/2011 | https://clinicaltrials.gov/study/NCT01436162 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Completed | 26/11/2012 | https://clinicaltrials.gov/study/NCT01718509 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Completed | 27/01/2014 | https://clinicaltrials.gov/study/NCT02009163 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Completed | 26/11/2012 | https://clinicaltrials.gov/study/NCT01718483 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 3 | Completed | 21/08/2012 | https://clinicaltrials.gov/study/NCT01657019 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | drug dependence | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a310fc51-2743-4755-8398-fed5402283f6 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | Completed | 01/07/2008 | https://clinicaltrials.gov/study/NCT00733356 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a310fc51-2743-4755-8398-fed5402283f6 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | Not yet recruiting | 01/08/2011 | https://clinicaltrials.gov/study/NCT01413165 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | Completed | 03/04/2012 | https://clinicaltrials.gov/study/NCT01552902 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | Completed | 07/07/2011 | https://clinicaltrials.gov/study/NCT01328756 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | Completed | 17/04/2012 | https://clinicaltrials.gov/study/NCT01552915 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE DIMESYLATE | targetBased | 4 | Completed | 30/04/2009 | https://clinicaltrials.gov/study/NCT00877487 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | sleep apnea | ARMODAFINIL | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00078312 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizoaffective disorder | ARMODAFINIL | targetBased | 4 | Completed | 01/08/2006 | https://clinicaltrials.gov/study/NCT00373672 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | hypersomnia | ARMODAFINIL | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00758498 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | hypersomnia | ARMODAFINIL | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00080288 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | hypersomnia | ARMODAFINIL | targetBased | 4 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00711516 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | hypersomnia | ARMODAFINIL | targetBased | 4 | Completed | 01/03/2010 | https://clinicaltrials.gov/study/NCT01080807 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Dementia | ARMODAFINIL | targetBased | 4 | Completed | 01/11/2009 | https://clinicaltrials.gov/study/NCT01023672 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | ARMODAFINIL | targetBased | 3 | Terminated | 30/04/2010 | https://clinicaltrials.gov/study/NCT01121536 | 0.7 | LoF | protect | Business decision related to efficacy rather than tolerability limitations, not stopped for any safety reasons. |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | ARMODAFINIL | targetBased | 3 | Completed | 01/03/2010 | https://clinicaltrials.gov/study/NCT01072630 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | ARMODAFINIL | targetBased | 3 | Completed | 01/01/2010 | https://clinicaltrials.gov/study/NCT01072929 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | ARMODAFINIL | targetBased | 3 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01305408 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | ARMODAFINIL | targetBased | 3 | Completed | 01/02/2004 | https://clinicaltrials.gov/study/NCT00078325 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | ARMODAFINIL | targetBased | 3 | Completed | 01/05/2004 | https://clinicaltrials.gov/study/NCT00228553 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | ARMODAFINIL | targetBased | 3 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT00228566 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=10f918f7-4782-470e-a50e-35c7c66bfd79 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | ARMODAFINIL | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00079677 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | obstructive sleep apnea | ARMODAFINIL | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00078312 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | ARMODAFINIL | targetBased | 4 | Completed | 01/08/2006 | https://clinicaltrials.gov/study/NCT00373672 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Sleep Disorder | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2c824d4c-2309-4e2a-bc74-aa8d80a5c454 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Sleep Disorder | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0310a062-51fd-4e74-8a5f-7f21a16f52c9 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Sleep Disorder | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=10f918f7-4782-470e-a50e-35c7c66bfd79 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Sleep Disorder | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a2b3b762-7984-409c-82e4-8d216055df72 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Sleep Disorder | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e7bfb636-4b0a-440c-a4d3-d26393a14ac5 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Sleep Disorder | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=795a7ba3-c60b-4637-aa99-06c1e10af8a7 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | Sleep Disorder | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d878aed0-ddbf-8fa1-abf7-d3e480260845 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2c824d4c-2309-4e2a-bc74-aa8d80a5c454 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0310a062-51fd-4e74-8a5f-7f21a16f52c9 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a2b3b762-7984-409c-82e4-8d216055df72 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=795a7ba3-c60b-4637-aa99-06c1e10af8a7 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e7bfb636-4b0a-440c-a4d3-d26393a14ac5 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d878aed0-ddbf-8fa1-abf7-d3e480260845 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | ARMODAFINIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=10f918f7-4782-470e-a50e-35c7c66bfd79 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy | ARMODAFINIL | targetBased | 3 | Completed | 01/01/2004 | https://clinicaltrials.gov/study/NCT00078312 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy | ARMODAFINIL | targetBased | 3 | Completed | 01/03/2004 | https://clinicaltrials.gov/study/NCT00078377 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy | ARMODAFINIL | targetBased | 3 | Completed | 01/05/2004 | https://clinicaltrials.gov/study/NCT00228553 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy | ARMODAFINIL | targetBased | 3 | Completed | 01/10/2005 | https://clinicaltrials.gov/study/NCT00228566 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | ARMODAFINIL | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06BA13 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | methamphetamine dependence | METHAMPHETAMINE | targetBased | 4 | Completed | 16/08/2019 | https://clinicaltrials.gov/study/NCT03973489 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHAMPHETAMINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06BA03 | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | METHAMPHETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f03a68d5-ed00-8a2d-af68-28be909ea85f | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | Agitation | BENZTROPINE | targetBased | 4 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00457366 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BENZTROPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT00802100 | 1 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BENZTROPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT00802100 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BENZTROPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT00802100 | 1 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BENZTROPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT00802100 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | schizophrenia | BENZTROPINE | targetBased | 4 | Completed | 01/12/2008 | https://clinicaltrials.gov/study/NCT00802100 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | binge eating | LISDEXAMFETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=704e4378-ca83-445c-8b45-3cfa51c1ecad | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | LISDEXAMFETAMINE | targetBased | 3 | Terminated | 01/01/2010 | https://clinicaltrials.gov/study/NCT01131559 | 0.7 | protect | Sponsor halted study. | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | depressive disorder | LISDEXAMFETAMINE | targetBased | 4 | Completed | 01/04/2013 | https://clinicaltrials.gov/study/NCT01863459 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | LISDEXAMFETAMINE | targetBased | 3 | Withdrawn | 27/01/2012 | https://clinicaltrials.gov/study/NCT01234298 | 0.7 | protect | Study was discontinued due to non-safety related business prioritization decisions | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | LISDEXAMFETAMINE | targetBased | 3 | Terminated | 01/02/2013 | https://clinicaltrials.gov/study/NCT01760889 | 0.7 | protect | Study was discontinued due to non-safety related business prioritization decisions. No subjects were randomized | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | LISDEXAMFETAMINE | targetBased | 3 | Terminated | 01/11/2012 | https://clinicaltrials.gov/study/NCT01738698 | 0.7 | protect | Study was discontinued due to non-safety related business prioritization decisions. No subjects were randomized. | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | schizophrenia | LISDEXAMFETAMINE | targetBased | 3 | Terminated | 01/02/2013 | https://clinicaltrials.gov/study/NCT01760993 | 0.7 | protect | Study was discontinued due to non-safety related business prioritization decisions. No subjects were randomized. | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | LISDEXAMFETAMINE | targetBased | 4 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01148979 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | LISDEXAMFETAMINE | targetBased | 3 | Completed | 27/10/2011 | https://clinicaltrials.gov/study/NCT01436149 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | LISDEXAMFETAMINE | targetBased | 3 | Terminated | 27/02/2012 | https://clinicaltrials.gov/study/NCT01436175 | 0.35 | protect | SPD489 failed to demonstrate a benefit as adjunctive treatment to antidepressants. Termination was not related to any new safety findings. | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | LISDEXAMFETAMINE | targetBased | 3 | Completed | 19/10/2011 | https://clinicaltrials.gov/study/NCT01436162 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | LISDEXAMFETAMINE | targetBased | 3 | Completed | 21/08/2012 | https://clinicaltrials.gov/study/NCT01657019 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | LISDEXAMFETAMINE | targetBased | 3 | Completed | 26/11/2012 | https://clinicaltrials.gov/study/NCT01718483 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | LISDEXAMFETAMINE | targetBased | 3 | Completed | 27/01/2014 | https://clinicaltrials.gov/study/NCT02009163 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | LISDEXAMFETAMINE | targetBased | 3 | Completed | 26/11/2012 | https://clinicaltrials.gov/study/NCT01718509 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | LISDEXAMFETAMINE | targetBased | 3 | Completed | 01/01/2010 | https://clinicaltrials.gov/study/NCT01090713 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | drug dependence | LISDEXAMFETAMINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a310fc51-2743-4755-8398-fed5402283f6 | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar disorder | LISDEXAMFETAMINE | targetBased | 3 | Terminated | 01/01/2010 | https://clinicaltrials.gov/study/NCT01093963 | 0.7 | protect | Enrollment goals not met | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | bipolar disorder | LISDEXAMFETAMINE | targetBased | 4 | Terminated | 01/02/2010 | https://clinicaltrials.gov/study/NCT01051440 | 1 | protect | Slow enrollment | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE | targetBased | 4 | Completed | 03/04/2012 | https://clinicaltrials.gov/study/NCT01552902 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE | targetBased | 4 | Completed | 19/05/2010 | https://clinicaltrials.gov/study/NCT01101022 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE | targetBased | 4 | Completed | 01/04/2008 | https://clinicaltrials.gov/study/NCT00753012 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE | targetBased | 4 | Completed | 30/04/2009 | https://clinicaltrials.gov/study/NCT00877487 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE | targetBased | 4 | Completed | 17/04/2012 | https://clinicaltrials.gov/study/NCT01552915 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE | targetBased | 4 | Completed | 01/07/2008 | https://clinicaltrials.gov/study/NCT00733356 | 1 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | LISDEXAMFETAMINE | targetBased | 4 | Completed | 01/04/2013 | https://clinicaltrials.gov/study/NCT01863459 | 1 | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol abuse | ACAMPROSATE | targetBased | 4 | Completed | 01/03/2007 | https://clinicaltrials.gov/study/NCT00452543 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | social anxiety disorder | ACAMPROSATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00330174 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | generalized anxiety disorder | ACAMPROSATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00330174 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | Dementia | ACAMPROSATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | ACAMPROSATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizophrenia | ACAMPROSATE | targetBased | 4 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00688324 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | anxiety | ACAMPROSATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00330174 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE | targetBased | 4 | Completed | 01/11/2009 | https://clinicaltrials.gov/study/NCT00855699 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE | targetBased | 4 | Unknown status | 01/03/2003 | https://clinicaltrials.gov/study/NCT00120601 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00466661 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE | targetBased | 4 | Completed | 01/09/2000 | https://clinicaltrials.gov/study/NCT00435435 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE | targetBased | 4 | Completed | 01/03/2007 | https://clinicaltrials.gov/study/NCT00452543 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE | targetBased | 4 | Completed | 01/11/2002 | https://clinicaltrials.gov/study/NCT00317031 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ACAMPROSATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00330174 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ACAMPROSATE | targetBased | 3 | Terminated | 01/01/2015 | https://clinicaltrials.gov/study/NCT02374567 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | bipolar disorder | ACAMPROSATE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00466661 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | schizoaffective disorder | ACAMPROSATE | targetBased | 4 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00688324 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | ACAMPROSATE | targetBased | 4 | Completed | 01/03/2007 | https://clinicaltrials.gov/study/NCT00452543 | 1 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | gambling behaviour | ACAMPROSATE | targetBased | 4 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00571103 | 1 | LoF | protect | ||
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | CHRM1 | Muscarinic acetylcholine receptor M1 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | CHRM1 | Muscarinic acetylcholine receptor M1 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | CHRM1 | Muscarinic acetylcholine receptor M1 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | CHRM1 | Muscarinic acetylcholine receptor M1 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | CHRM1 | Muscarinic acetylcholine receptor M1 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_PAMs | CHRM4 | Muscarinic acetylcholine receptor M4 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_antgonists | CHRM4 | Muscarinic acetylcholine receptor M4 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_agonists | CHRM4 | Muscarinic acetylcholine receptor M4 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 5 (CHRM5) | CHRM5 | CHRM5 | Muscarinic acetylcholine receptor M5 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human cholinergic receptor, muscarinic 5 (CHRM5) | CHRM5 | CHRM5 | Muscarinic acetylcholine receptor M5 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human cholinergic receptor, muscarinic 5 (CHRM5) | CHRM5 | CHRM5 | Muscarinic acetylcholine receptor M5 | delirium | GLYCOPYRRONIUM | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03229486 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | nicotine dependence | BUPROPION HYDROBROMIDE | targetBased | 4 | Completed | 01/07/2009 | https://clinicaltrials.gov/study/NCT00991081 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | major depressive disorder | BUPROPION HYDROBROMIDE | targetBased | 4 | Not yet recruiting | 01/06/2023 | https://clinicaltrials.gov/study/NCT02129751 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROBROMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2315d6e5-144d-4163-9711-f855c759cf8e | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROBROMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6494d2d9-0ce4-4126-b1c7-49684395942b | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | unipolar depression | BUPROPION HYDROBROMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5cb7fd36-ae36-409b-af79-9c432e1cf5d9 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHYLNALTREXONE BROMIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/relistor | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | METHYLNALTREXONE BROMIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/relistor | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | LURASIDONE | targetBased | 3 | Withdrawn | 01/01/2012 | https://clinicaltrials.gov/study/NCT01423240 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01421134 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01423253 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE | targetBased | 4 | Terminated | 30/12/2021 | https://clinicaltrials.gov/study/NCT05213143 | 1 | LoF | protect | Company's business decision |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE | targetBased | 4 | Completed | 16/08/2021 | https://clinicaltrials.gov/study/NCT05011669 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01569659 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE | targetBased | 4 | Unknown status | 01/12/2014 | https://clinicaltrials.gov/study/NCT02282085 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE | targetBased | 4 | Completed | 07/02/2019 | https://clinicaltrials.gov/study/NCT03902613 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE | targetBased | 4 | Withdrawn | 01/01/2017 | https://clinicaltrials.gov/study/NCT01932541 | 1 | LoF | protect | On hold due to competing departmental studies |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE | targetBased | 4 | Withdrawn | 01/01/2017 | https://clinicaltrials.gov/study/NCT01932541 | 1 | LoF | protect | On hold due to competing departmental studies |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE | targetBased | 4 | Withdrawn | 01/01/2017 | https://clinicaltrials.gov/study/NCT01932541 | 1 | LoF | protect | On hold due to competing departmental studies |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE | targetBased | 4 | Withdrawn | 01/01/2017 | https://clinicaltrials.gov/study/NCT01932541 | 1 | LoF | protect | On hold due to competing departmental studies |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE | targetBased | 4 | Withdrawn | 01/01/2017 | https://clinicaltrials.gov/study/NCT01932541 | 1 | LoF | protect | On hold due to competing departmental studies |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE | targetBased | 4 | Withdrawn | 01/01/2017 | https://clinicaltrials.gov/study/NCT01932541 | 1 | LoF | protect | On hold due to competing departmental studies |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | LURASIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01423253 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01423253 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01423253 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01423253 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Withdrawn | 01/01/2012 | https://clinicaltrials.gov/study/NCT01423240 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Withdrawn | 01/01/2012 | https://clinicaltrials.gov/study/NCT01423240 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Withdrawn | 01/01/2012 | https://clinicaltrials.gov/study/NCT01423240 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Withdrawn | 01/01/2012 | https://clinicaltrials.gov/study/NCT01423240 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Withdrawn | 01/01/2012 | https://clinicaltrials.gov/study/NCT01423240 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LURASIDONE | targetBased | 3 | Withdrawn | 01/01/2012 | https://clinicaltrials.gov/study/NCT01423240 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/03/2014 | https://clinicaltrials.gov/study/NCT02046369 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/03/2014 | https://clinicaltrials.gov/study/NCT02046369 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/03/2014 | https://clinicaltrials.gov/study/NCT02046369 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/03/2014 | https://clinicaltrials.gov/study/NCT02046369 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Terminated | 11/12/2020 | https://clinicaltrials.gov/study/NCT04383691 | 0.7 | LoF | protect | Company's business decision |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Terminated | 11/12/2020 | https://clinicaltrials.gov/study/NCT04383691 | 0.7 | LoF | protect | Company's business decision |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Terminated | 11/12/2020 | https://clinicaltrials.gov/study/NCT04383691 | 0.7 | LoF | protect | Company's business decision |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Terminated | 11/12/2020 | https://clinicaltrials.gov/study/NCT04383691 | 0.7 | LoF | protect | Company's business decision |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Terminated | 11/12/2020 | https://clinicaltrials.gov/study/NCT04383691 | 0.7 | LoF | protect | Company's business decision |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | LURASIDONE | targetBased | 3 | Terminated | 11/12/2020 | https://clinicaltrials.gov/study/NCT04383691 | 0.7 | LoF | protect | Company's business decision |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LURASIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LURASIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LURASIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LURASIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LURASIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LURASIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LURASIDONE | targetBased | 3 | Completed | 01/06/2010 | https://clinicaltrials.gov/study/NCT01143077 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01575561 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 01/05/2014 | https://clinicaltrials.gov/study/NCT02147379 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01358357 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE | targetBased | 4 | Withdrawn | 01/01/2017 | https://clinicaltrials.gov/study/NCT01932541 | 1 | LoF | protect | On hold due to competing departmental studies |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE | targetBased | 3 | Completed | 01/04/2009 | https://clinicaltrials.gov/study/NCT00868452 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE | targetBased | 4 | Completed | 07/02/2019 | https://clinicaltrials.gov/study/NCT03902613 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE | targetBased | 3 | Completed | 01/04/2009 | https://clinicaltrials.gov/study/NCT00868959 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE | targetBased | 3 | Completed | 01/11/2010 | https://clinicaltrials.gov/study/NCT01284517 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE | targetBased | 3 | Recruiting | 08/05/2017 | https://clinicaltrials.gov/study/NCT02731612 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE | targetBased | 3 | Completed | 01/04/2009 | https://clinicaltrials.gov/study/NCT00868699 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE | targetBased | 3 | Completed | 19/02/2014 | https://clinicaltrials.gov/study/NCT01986101 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | LURASIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | LURASIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | LURASIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | LURASIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | LURASIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | LURASIDONE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | LURASIDONE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AE05 | 0.7 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | LURASIDONE | targetBased | 3 | Completed | 01/06/2010 | https://clinicaltrials.gov/study/NCT01143077 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | LURASIDONE | targetBased | 4 | Completed | 01/02/2013 | https://clinicaltrials.gov/study/NCT02199743 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | LURASIDONE | targetBased | 3 | Completed | 01/08/2010 | https://clinicaltrials.gov/study/NCT01143090 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | LURASIDONE | targetBased | 3 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00641745 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | LURASIDONE | targetBased | 3 | Terminated | 11/12/2020 | https://clinicaltrials.gov/study/NCT04383691 | 0.7 | LoF | protect | Company's business decision |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | LURASIDONE | targetBased | 3 | Completed | 01/03/2014 | https://clinicaltrials.gov/study/NCT02046369 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | LURASIDONE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AE05 | 0.7 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | LURASIDONE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AE05 | 0.7 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | LURASIDONE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AE05 | 0.7 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | LURASIDONE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AE05 | 0.7 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | LURASIDONE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AE05 | 0.7 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | LURASIDONE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N05AE05 | 0.7 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | autism | LURASIDONE | targetBased | 3 | Completed | 01/08/2013 | https://clinicaltrials.gov/study/NCT01911442 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 01/05/2014 | https://clinicaltrials.gov/study/NCT02147379 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 01/05/2014 | https://clinicaltrials.gov/study/NCT02147379 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 01/05/2014 | https://clinicaltrials.gov/study/NCT02147379 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 01/05/2014 | https://clinicaltrials.gov/study/NCT02147379 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE | targetBased | 4 | Terminated | 30/12/2021 | https://clinicaltrials.gov/study/NCT05213143 | 1 | LoF | protect | Company's business decision |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE | targetBased | 4 | Completed | 03/01/2018 | https://clinicaltrials.gov/study/NCT03393026 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE | targetBased | 4 | Completed | 03/01/2018 | https://clinicaltrials.gov/study/NCT03393026 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE | targetBased | 4 | Completed | 03/01/2018 | https://clinicaltrials.gov/study/NCT03393026 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE | targetBased | 4 | Completed | 03/01/2018 | https://clinicaltrials.gov/study/NCT03393026 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE | targetBased | 4 | Completed | 03/01/2018 | https://clinicaltrials.gov/study/NCT03393026 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE | targetBased | 4 | Completed | 03/01/2018 | https://clinicaltrials.gov/study/NCT03393026 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism | LURASIDONE | targetBased | 3 | Completed | 01/08/2013 | https://clinicaltrials.gov/study/NCT01911442 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism | LURASIDONE | targetBased | 3 | Completed | 01/08/2013 | https://clinicaltrials.gov/study/NCT01911442 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism | LURASIDONE | targetBased | 3 | Completed | 01/08/2013 | https://clinicaltrials.gov/study/NCT01911442 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism | LURASIDONE | targetBased | 3 | Completed | 01/08/2013 | https://clinicaltrials.gov/study/NCT01911442 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | LURASIDONE | targetBased | 3 | Completed | 01/08/2013 | https://clinicaltrials.gov/study/NCT01911442 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism | LURASIDONE | targetBased | 3 | Completed | 01/08/2013 | https://clinicaltrials.gov/study/NCT01911442 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | TRAMADOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b3c702f7-0a8c-a52b-e053-2995a90a6df3 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | TRAMADOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b3c702f7-0a8c-a52b-e053-2995a90a6df3 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | TRAMADOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3da3815b-fa99-4b20-8564-96d32d84df28 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | TRAMADOL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3da3815b-fa99-4b20-8564-96d32d84df28 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | post-traumatic stress disorder | TRAMADOL | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01517711 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | post-traumatic stress disorder | TRAMADOL | targetBased | 4 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01517711 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | TRAMADOL | targetBased | 4 | Terminated | 17/05/2021 | https://clinicaltrials.gov/study/NCT04766996 | 1 | GoF | protect | Loss of surgery team member deemed the study procedures impossible to achieve, and no replacement could be found in a timely manner to complete trial as initially planned. |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | TRAMADOL | targetBased | 4 | Terminated | 17/05/2021 | https://clinicaltrials.gov/study/NCT04766996 | 1 | GoF | protect | Loss of surgery team member deemed the study procedures impossible to achieve, and no replacement could be found in a timely manner to complete trial as initially planned. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | TRAMADOL | targetBased | 3 | Withdrawn | 15/11/2019 | https://clinicaltrials.gov/study/NCT03678792 | 0.7 | GoF | protect | Infeasible to conduct at this time. |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | TRAMADOL | targetBased | 3 | Withdrawn | 15/11/2019 | https://clinicaltrials.gov/study/NCT03678792 | 0.7 | GoF | protect | Infeasible to conduct at this time. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | sleep apnea | TRAMADOL | targetBased | 4 | Completed | 01/03/2018 | https://clinicaltrials.gov/study/NCT03454217 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | sleep apnea | TRAMADOL | targetBased | 4 | Completed | 01/03/2018 | https://clinicaltrials.gov/study/NCT03454217 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3832ede8-d3fc-455d-ecab-3b77be5869f5 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3832ede8-d3fc-455d-ecab-3b77be5869f5 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=22e635cb-98c0-e4f9-6a71-62d7487a0a6c | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=22e635cb-98c0-e4f9-6a71-62d7487a0a6c | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b95bfd6c-cee5-f57d-e053-2995a90a5ce1 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROMORPHONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b95bfd6c-cee5-f57d-e053-2995a90a5ce1 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | TRAMADOL HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3da3815b-fa99-4b20-8564-96d32d84df28 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | TRAMADOL HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3da3815b-fa99-4b20-8564-96d32d84df28 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | TRAMADOL HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b3c702f7-0a8c-a52b-e053-2995a90a6df3 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | TRAMADOL HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b3c702f7-0a8c-a52b-e053-2995a90a6df3 | 1 | GoF | protect | |||
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | nicotine dependence | FORMOTEROL | targetBased | 3 | Completed | 01/05/2017 | https://clinicaltrials.gov/study/NCT03104634 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety disorder | TRIFLUOPERAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=09dc7f6a-cc69-4de8-8e13-b837ce144b4a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | ESMIRTAZAPINE | targetBased | 3 | Completed | 06/06/2007 | https://clinicaltrials.gov/study/NCT00506389 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | ESMIRTAZAPINE | targetBased | 3 | Completed | 07/12/2006 | https://clinicaltrials.gov/study/NCT00482612 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | ESMIRTAZAPINE | targetBased | 3 | Completed | 07/12/2006 | https://clinicaltrials.gov/study/NCT00610675 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4890cf77-8da3-46ae-b6f6-abea7aae6b4d | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f8ff266-c144-4843-9d05-d6276bde2f4d | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0090b65d-d663-4588-b0e6-e6fc903ca18c | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=75e6a13c-39a7-4df0-b39a-b65b8bd7f618 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=315e24c2-2f8c-47d9-b1b1-ce006646098a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4282fe5b-9e3c-49e5-8670-b2a2c1b7b207 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f8ff266-c144-4843-9d05-d6276bde2f4d | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8326928a-2cb6-4f7f-9712-03a425a14c37 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=819997d8-e091-4081-85e1-bf50d39837ee | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | FLUPHENAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=50c7e742-1165-4c45-bbf6-172cf70a387a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 01/08/2012 | https://clinicaltrials.gov/study/NCT01614912 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 02/07/2012 | https://clinicaltrials.gov/study/NCT01614899 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=88a244d1-eddb-499c-bee2-e1f49056e78f | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 19/02/2014 | https://clinicaltrials.gov/study/NCT01986101 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 19/02/2014 | https://clinicaltrials.gov/study/NCT01986101 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | LURASIDONE HYDROCHLORIDE | targetBased | 3 | Completed | 29/01/2014 | https://clinicaltrials.gov/study/NCT01986114 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=afad3051-9df2-4c54-9684-e8262a133af8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=88a244d1-eddb-499c-bee2-e1f49056e78f | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=88a244d1-eddb-499c-bee2-e1f49056e78f | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=88a244d1-eddb-499c-bee2-e1f49056e78f | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=88a244d1-eddb-499c-bee2-e1f49056e78f | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=88a244d1-eddb-499c-bee2-e1f49056e78f | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LURASIDONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=88a244d1-eddb-499c-bee2-e1f49056e78f | 1 | LoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VILAZODONE HYDROCHLORIDE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01715519 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VILAZODONE HYDROCHLORIDE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01715519 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | VILAZODONE HYDROCHLORIDE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01715519 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | VILAZODONE HYDROCHLORIDE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01715519 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c55ccfb-c4cf-11df-851a-0800200c9a66 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c55ccfb-c4cf-11df-851a-0800200c9a66 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bfef9e19-d0f5-40fa-954c-b73c812eb242 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VILAZODONE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bfef9e19-d0f5-40fa-954c-b73c812eb242 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | unipolar depression | ATICAPRANT | targetBased | 3 | Recruiting | 22/06/2022 | https://clinicaltrials.gov/study/NCT05455684 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | unipolar depression | ATICAPRANT | targetBased | 3 | Recruiting | 22/09/2022 | https://clinicaltrials.gov/study/NCT05518149 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 13/12/2022 | https://clinicaltrials.gov/study/NCT05913947 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 13/12/2022 | https://clinicaltrials.gov/study/NCT05913947 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 13/12/2022 | https://clinicaltrials.gov/study/NCT05913947 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 31/03/2024 | https://clinicaltrials.gov/study/NCT05060549 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 31/03/2024 | https://clinicaltrials.gov/study/NCT05060549 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 31/03/2024 | https://clinicaltrials.gov/study/NCT05060549 | 1 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 31/03/2024 | https://clinicaltrials.gov/study/NCT05060549 | 1 | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 31/03/2024 | https://clinicaltrials.gov/study/NCT05060549 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 31/03/2024 | https://clinicaltrials.gov/study/NCT05060549 | 1 | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 31/03/2024 | https://clinicaltrials.gov/study/NCT05060549 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 31/03/2024 | https://clinicaltrials.gov/study/NCT05060549 | 1 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 31/03/2024 | https://clinicaltrials.gov/study/NCT05060549 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05933538 | 1 | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05933538 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05933538 | 1 | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05933538 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05933538 | 1 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05933538 | 1 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 29/04/2013 | https://clinicaltrials.gov/study/NCT01838876 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | psychosis | CARIPRAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX15 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | psychosis | CARIPRAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX15 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | psychosis | CARIPRAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX15 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | autism spectrum disorder | CARIPRAZINE | targetBased | 3 | Recruiting | 07/07/2022 | https://clinicaltrials.gov/study/NCT05439616 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | autism spectrum disorder | CARIPRAZINE | targetBased | 3 | Recruiting | 07/07/2022 | https://clinicaltrials.gov/study/NCT05439616 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | autism spectrum disorder | CARIPRAZINE | targetBased | 3 | Recruiting | 07/07/2022 | https://clinicaltrials.gov/study/NCT05439616 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | major depressive disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05933538 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | major depressive disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05933538 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | major depressive disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 01/08/2024 | https://clinicaltrials.gov/study/NCT05933538 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | major depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 29/04/2013 | https://clinicaltrials.gov/study/NCT01838876 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | major depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 29/04/2013 | https://clinicaltrials.gov/study/NCT01838876 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | major depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 29/04/2013 | https://clinicaltrials.gov/study/NCT01838876 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | major depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/11/2012 | https://clinicaltrials.gov/study/NCT01715805 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | major depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/11/2012 | https://clinicaltrials.gov/study/NCT01715805 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | major depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/11/2012 | https://clinicaltrials.gov/study/NCT01715805 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 17/03/2016 | https://clinicaltrials.gov/study/NCT02670551 | 0.7 | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 17/03/2016 | https://clinicaltrials.gov/study/NCT02670551 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 17/03/2016 | https://clinicaltrials.gov/study/NCT02670551 | 0.7 | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 17/03/2016 | https://clinicaltrials.gov/study/NCT02670551 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 17/03/2016 | https://clinicaltrials.gov/study/NCT02670551 | 0.7 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 17/03/2016 | https://clinicaltrials.gov/study/NCT02670551 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/reagila | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | CARIPRAZINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 31/03/2016 | https://clinicaltrials.gov/study/NCT02670538 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 31/03/2016 | https://clinicaltrials.gov/study/NCT02670538 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 31/03/2016 | https://clinicaltrials.gov/study/NCT02670538 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 17/03/2016 | https://clinicaltrials.gov/study/NCT02670551 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 17/03/2016 | https://clinicaltrials.gov/study/NCT02670551 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 17/03/2016 | https://clinicaltrials.gov/study/NCT02670551 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | depressive disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | CARIPRAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX15 | 1 | protect | ||||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | CARIPRAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX15 | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | CARIPRAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX15 | 1 | protect | ||||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | CARIPRAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX15 | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | CARIPRAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX15 | 1 | protect | ||||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | CARIPRAZINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX15 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE | targetBased | 3 | Completed | 01/02/2010 | https://clinicaltrials.gov/study/NCT01058668 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE | targetBased | 3 | Completed | 01/02/2010 | https://clinicaltrials.gov/study/NCT01058668 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE | targetBased | 3 | Completed | 01/02/2010 | https://clinicaltrials.gov/study/NCT01058668 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | bipolar I disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | social anxiety disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 15/07/2022 | https://clinicaltrials.gov/study/NCT05384483 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | social anxiety disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 15/07/2022 | https://clinicaltrials.gov/study/NCT05384483 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | social anxiety disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 15/07/2022 | https://clinicaltrials.gov/study/NCT05384483 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | CARIPRAZINE | targetBased | 3 | Recruiting | 07/07/2022 | https://clinicaltrials.gov/study/NCT05439616 | 0.7 | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | CARIPRAZINE | targetBased | 3 | Recruiting | 07/07/2022 | https://clinicaltrials.gov/study/NCT05439616 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism spectrum disorder | CARIPRAZINE | targetBased | 3 | Recruiting | 07/07/2022 | https://clinicaltrials.gov/study/NCT05439616 | 0.7 | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | autism spectrum disorder | CARIPRAZINE | targetBased | 3 | Recruiting | 07/07/2022 | https://clinicaltrials.gov/study/NCT05439616 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | CARIPRAZINE | targetBased | 3 | Recruiting | 07/07/2022 | https://clinicaltrials.gov/study/NCT05439616 | 0.7 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | autism spectrum disorder | CARIPRAZINE | targetBased | 3 | Recruiting | 07/07/2022 | https://clinicaltrials.gov/study/NCT05439616 | 0.7 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3435ec73-86ed-46d1-bd1f-ee6c30209123 | 1 | protect | ||||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | CARIPRAZINE | targetBased | 3 | Completed | 15/06/2018 | https://clinicaltrials.gov/study/NCT03573297 | 0.7 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b5f7c65-aa2d-452a-b3db-bc85c06ff12f | 1 | protect | ||||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | CARIPRAZINE | targetBased | 4 | Recruiting | 16/08/2023 | https://clinicaltrials.gov/study/NCT05741502 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT04843423 | 1 | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT04843423 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT04843423 | 1 | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT04843423 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT04843423 | 1 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | attention deficit hyperactivity disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT04843423 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | attention deficit hyperactivity disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT04843423 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | attention deficit hyperactivity disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT04843423 | 1 | protect | ||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | attention deficit hyperactivity disorder | CARIPRAZINE | targetBased | 4 | Recruiting | 01/12/2021 | https://clinicaltrials.gov/study/NCT04843423 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 15/07/2022 | https://clinicaltrials.gov/study/NCT05384483 | 1 | protect | ||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 15/07/2022 | https://clinicaltrials.gov/study/NCT05384483 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | social anxiety disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 15/07/2022 | https://clinicaltrials.gov/study/NCT05384483 | 1 | protect | ||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | social anxiety disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 15/07/2022 | https://clinicaltrials.gov/study/NCT05384483 | 1 | protect | ||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 15/07/2022 | https://clinicaltrials.gov/study/NCT05384483 | 1 | protect | ||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | CARIPRAZINE | targetBased | 4 | Not yet recruiting | 15/07/2022 | https://clinicaltrials.gov/study/NCT05384483 | 1 | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE CALCIUM | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fe6f754f-62b4-4c86-805d-221332409516 | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE CALCIUM | targetBased | 3 | Completed | 05/08/2020 | https://clinicaltrials.gov/study/NCT03634917 | 0.7 | LoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | alcohol dependence | ACAMPROSATE CALCIUM | targetBased | 4 | Not yet recruiting | 08/07/2024 | https://clinicaltrials.gov/study/NCT06269627 | 1 | LoF | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R | MC4R | MC4R | Melanocortin receptor 4 | mental or behavioural disorder | BREMELANOTIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9146ae05-918b-483e-b86d-933485ce36eb | 1 | GoF | protect | |||
TRFRET-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): antagonists of MC4R | MC4R | MC4R | Melanocortin receptor 4 | mental or behavioural disorder | BREMELANOTIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9146ae05-918b-483e-b86d-933485ce36eb | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MORPHINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=83497476-dea9-57ec-e053-2991aa0a08c1 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MORPHINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=83497476-dea9-57ec-e053-2991aa0a08c1 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MORPHINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=533034fd-c8e7-495b-8874-0db41bd1e65a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | MORPHINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=533034fd-c8e7-495b-8874-0db41bd1e65a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | MORPHINE SULFATE | targetBased | 3 | Terminated | 20/05/2016 | https://clinicaltrials.gov/study/NCT03127800 | 0.7 | GoF | protect | Difficulties with recruitment |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | obstructive sleep apnea | MORPHINE SULFATE | targetBased | 3 | Terminated | 20/05/2016 | https://clinicaltrials.gov/study/NCT03127800 | 0.7 | GoF | protect | Difficulties with recruitment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE SULFATE | targetBased | 3 | Terminated | 06/12/2019 | https://clinicaltrials.gov/study/NCT03948464 | 0.7 | GoF | protect | Study unable to proceed per protocol due to COVID-19 precautions |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE SULFATE | targetBased | 3 | Terminated | 06/12/2019 | https://clinicaltrials.gov/study/NCT03948464 | 0.7 | GoF | protect | Study unable to proceed per protocol due to COVID-19 precautions |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE SULFATE | targetBased | 4 | Terminated | 14/09/2016 | https://clinicaltrials.gov/study/NCT02741076 | 1 | GoF | protect | Inability to recruit sufficient no. of subjects over an acceptable time period |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | MORPHINE SULFATE | targetBased | 4 | Terminated | 14/09/2016 | https://clinicaltrials.gov/study/NCT02741076 | 1 | GoF | protect | Inability to recruit sufficient no. of subjects over an acceptable time period |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | overdose | MORPHINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=533034fd-c8e7-495b-8874-0db41bd1e65a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | overdose | MORPHINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=533034fd-c8e7-495b-8874-0db41bd1e65a | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | MORPHINE SULFATE | targetBased | 4 | Recruiting | 21/02/2018 | https://clinicaltrials.gov/study/NCT03092011 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | neonatal abstinence syndrome | MORPHINE SULFATE | targetBased | 4 | Recruiting | 21/02/2018 | https://clinicaltrials.gov/study/NCT03092011 | 1 | GoF | protect | |
Modulation of AMPAR-stargazin complexes | AMPAStargazinComplexModulators | CACNG2 | Voltage-dependent calcium channel gamma-2 subunit | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00658372 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Modulation of AMPAR-stargazin complexes | AMPAStargazinComplexModulators | CACNG2 | Voltage-dependent calcium channel gamma-2 subunit | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00542685 | 0.7 | protect | ||
Modulation of AMPAR-stargazin complexes | AMPAStargazinComplexModulators | CACNG2 | Voltage-dependent calcium channel gamma-2 subunit | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/04/2008 | https://clinicaltrials.gov/study/NCT00658008 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Modulation of AMPAR-stargazin complexes | AMPAStargazinComplexModulators | CACNG2 | Voltage-dependent calcium channel gamma-2 subunit | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/10/2008 | https://clinicaltrials.gov/study/NCT00735267 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Modulation of AMPAR-stargazin complexes | AMPAStargazinComplexModulators | CACNG2 | Voltage-dependent calcium channel gamma-2 subunit | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Withdrawn | 01/01/2009 | https://clinicaltrials.gov/study/NCT00738738 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Modulation of AMPAR-stargazin complexes | AMPAStargazinComplexModulators | CACNG2 | Voltage-dependent calcium channel gamma-2 subunit | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00658762 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Modulation of AMPAR-stargazin complexes | AMPAStargazinComplexModulators | CACNG2 | Voltage-dependent calcium channel gamma-2 subunit | anxiety | IMAGABALIN | targetBased | 3 | Terminated | 01/10/2008 | https://clinicaltrials.gov/study/NCT00836069 | 0.7 | protect | Pfizer has terminated the execution of this protocol | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/10/2008 | https://clinicaltrials.gov/study/NCT00735267 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00658762 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Withdrawn | 01/01/2009 | https://clinicaltrials.gov/study/NCT00738738 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00542685 | 0.7 | protect | ||
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00658372 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/04/2008 | https://clinicaltrials.gov/study/NCT00658008 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | CACNA1H_inhibitors | CACNA1H | Voltage-dependent T-type calcium channel subunit alpha-1H | anxiety | IMAGABALIN | targetBased | 3 | Terminated | 01/10/2008 | https://clinicaltrials.gov/study/NCT00836069 | 0.7 | protect | Pfizer has terminated the execution of this protocol | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | anxiety | IMAGABALIN | targetBased | 3 | Terminated | 01/10/2008 | https://clinicaltrials.gov/study/NCT00836069 | 0.7 | protect | Pfizer has terminated the execution of this protocol | |
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B_modulators | CACNA1B | Voltage-dependent N-type calcium channel subunit alpha-1D | anxiety | IMAGABALIN | targetBased | 3 | Terminated | 01/10/2008 | https://clinicaltrials.gov/study/NCT00836069 | 0.7 | protect | Pfizer has terminated the execution of this protocol | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/04/2008 | https://clinicaltrials.gov/study/NCT00658008 | 0.7 | protect | Please see Detailed Description for termination reason. | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Withdrawn | 01/01/2009 | https://clinicaltrials.gov/study/NCT00738738 | 0.7 | protect | Please see Detailed Description for termination reason. | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00658762 | 0.7 | protect | Please see Detailed Description for termination reason. | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/10/2008 | https://clinicaltrials.gov/study/NCT00735267 | 0.7 | protect | Please see Detailed Description for termination reason. | |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00542685 | 0.7 | protect | ||
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | CACNA1D | Voltage-dependent N-type calcium channel subunit alpha-1B | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00658372 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | CACNA1H_inhibitors | CACNA1H | Voltage-dependent T-type calcium channel subunit alpha-1H | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/04/2008 | https://clinicaltrials.gov/study/NCT00658008 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | CACNA1H_inhibitors | CACNA1H | Voltage-dependent T-type calcium channel subunit alpha-1H | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00658762 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | CACNA1H_inhibitors | CACNA1H | Voltage-dependent T-type calcium channel subunit alpha-1H | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Withdrawn | 01/01/2009 | https://clinicaltrials.gov/study/NCT00738738 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | CACNA1H_inhibitors | CACNA1H | Voltage-dependent T-type calcium channel subunit alpha-1H | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Completed | 01/10/2007 | https://clinicaltrials.gov/study/NCT00542685 | 0.7 | protect | ||
Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | CACNA1H_inhibitors | CACNA1H | Voltage-dependent T-type calcium channel subunit alpha-1H | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/10/2008 | https://clinicaltrials.gov/study/NCT00735267 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | CACNA1H_inhibitors | CACNA1H | Voltage-dependent T-type calcium channel subunit alpha-1H | generalized anxiety disorder | IMAGABALIN | targetBased | 3 | Terminated | 01/05/2008 | https://clinicaltrials.gov/study/NCT00658372 | 0.7 | protect | Please see Detailed Description for termination reason. | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Mental deterioration | VORTIOXETINE | targetBased | 4 | Completed | 31/08/2016 | https://clinicaltrials.gov/study/NCT03272711 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Mental deterioration | VORTIOXETINE | targetBased | 4 | Completed | 31/08/2016 | https://clinicaltrials.gov/study/NCT03272711 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/03/2022 | https://clinicaltrials.gov/study/NCT05481957 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/03/2022 | https://clinicaltrials.gov/study/NCT05481957 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VORTIOXETINE | targetBased | 3 | Terminated | 10/08/2021 | https://clinicaltrials.gov/study/NCT05014919 | 0.7 | GoF | protect | The study was terminated based on new efficacy data from another study. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VORTIOXETINE | targetBased | 3 | Terminated | 10/08/2021 | https://clinicaltrials.gov/study/NCT05014919 | 0.7 | GoF | protect | The study was terminated based on new efficacy data from another study. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VORTIOXETINE | targetBased | 4 | Recruiting | 20/11/2019 | https://clinicaltrials.gov/study/NCT04301492 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VORTIOXETINE | targetBased | 4 | Recruiting | 20/11/2019 | https://clinicaltrials.gov/study/NCT04301492 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VORTIOXETINE | targetBased | 3 | Withdrawn | 01/10/2016 | https://clinicaltrials.gov/study/NCT02845349 | 0.7 | GoF | protect | Funding withdrawn. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | VORTIOXETINE | targetBased | 3 | Withdrawn | 01/10/2016 | https://clinicaltrials.gov/study/NCT02845349 | 0.7 | GoF | protect | Funding withdrawn. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/12/2016 | https://clinicaltrials.gov/study/NCT02637895 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/12/2016 | https://clinicaltrials.gov/study/NCT02637895 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VORTIOXETINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1a5b68e2-14d0-419d-9ec6-1ca97145e838 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/12/2016 | https://clinicaltrials.gov/study/NCT02749721 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/12/2016 | https://clinicaltrials.gov/study/NCT02749721 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VORTIOXETINE | targetBased | 4 | Completed | 10/02/2015 | https://clinicaltrials.gov/study/NCT02371980 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VORTIOXETINE | targetBased | 4 | Completed | 10/02/2015 | https://clinicaltrials.gov/study/NCT02371980 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02332954 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02332954 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | panic disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02395510 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | panic disorder | VORTIOXETINE | targetBased | 4 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02395510 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VORTIOXETINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b0700c9-b417-4c3a-b36f-de461e125bd3 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VORTIOXETINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b0700c9-b417-4c3a-b36f-de461e125bd3 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VORTIOXETINE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N06AX26 | 0.7 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VORTIOXETINE | targetBased | 3 | https://www.whocc.no/atc_ddd_index/?code=N06AX26 | 0.7 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VORTIOXETINE | targetBased | 4 | Terminated | 24/08/2017 | https://clinicaltrials.gov/study/NCT02969876 | 1 | GoF | protect | Site was unable to reach Sponsor recruitment goals. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VORTIOXETINE | targetBased | 4 | Terminated | 24/08/2017 | https://clinicaltrials.gov/study/NCT02969876 | 1 | GoF | protect | Site was unable to reach Sponsor recruitment goals. |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | VORTIOXETINE | targetBased | 4 | Active, not recruiting | 01/02/2016 | https://clinicaltrials.gov/study/NCT02357797 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | VORTIOXETINE | targetBased | 4 | Active, not recruiting | 01/02/2016 | https://clinicaltrials.gov/study/NCT02357797 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | VORTIOXETINE | targetBased | 4 | Completed | 27/12/2019 | https://clinicaltrials.gov/study/NCT04220996 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | anxiety | VORTIOXETINE | targetBased | 4 | Completed | 27/12/2019 | https://clinicaltrials.gov/study/NCT04220996 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00788034 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00788034 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00744627 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00744627 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00730691 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00730691 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00731120 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00731120 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00734071 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | generalized anxiety disorder | VORTIOXETINE | targetBased | 3 | Completed | 01/06/2008 | https://clinicaltrials.gov/study/NCT00734071 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | VERALIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL06 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | VERALIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | VERALIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL06 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | VERALIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL06 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | VERALIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL06 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | VERALIPRIDE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AL06 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | schizophrenia | SAMIDORPHAN L-MALATE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | schizophrenia | SAMIDORPHAN L-MALATE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | bipolar I disorder | SAMIDORPHAN L-MALATE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | bipolar I disorder | SAMIDORPHAN L-MALATE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | bipolar I disorder | SAMIDORPHAN L-MALATE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | LoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | schizophrenia | SAMIDORPHAN L-MALATE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/213378s000lbl.pdf | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Sleep Disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01942733 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/04/2021 | https://clinicaltrials.gov/study/NCT04830215 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Recruiting | 20/01/2023 | https://clinicaltrials.gov/study/NCT05017311 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 04/10/2018 | https://clinicaltrials.gov/study/NCT03737474 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02196506 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Withdrawn | 01/09/2014 | https://clinicaltrials.gov/study/NCT02212613 | 0.7 | LoF | protect | Low enrollment |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Withdrawn | 29/08/2022 | https://clinicaltrials.gov/study/NCT05504486 | 1 | LoF | protect | Sponsor strategic decision |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 13/07/2018 | https://clinicaltrials.gov/study/NCT03538691 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Terminated | 01/12/2013 | https://clinicaltrials.gov/study/NCT01987960 | 0.7 | LoF | protect | The study was terminated due to challenges with patient eligibility; the decision to terminate was not based on any safety concerns |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/10/2019 | https://clinicaltrials.gov/study/NCT04174170 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 17/10/2019 | https://clinicaltrials.gov/study/NCT04124614 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02196506 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02196506 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01360632 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01360632 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | LoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | BREXPIPRAZOLE | targetBased | 3 | Recruiting | 10/05/2021 | https://clinicaltrials.gov/study/NCT04569448 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | BREXPIPRAZOLE | targetBased | 3 | Recruiting | 10/05/2021 | https://clinicaltrials.gov/study/NCT04569448 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03427892 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03427892 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/rxulti | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Active, not recruiting | 23/08/2017 | https://clinicaltrials.gov/study/NCT03238326 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Withdrawn | 01/06/2016 | https://clinicaltrials.gov/study/NCT02758067 | 0.7 | LoF | protect | This study was withdrawn for administrative reasons. There were no safety concerns. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2011 | https://clinicaltrials.gov/study/NCT01396421 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Recruiting | 31/05/2022 | https://clinicaltrials.gov/study/NCT05326347 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/06/2017 | https://clinicaltrials.gov/study/NCT03198078 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/11/2013 | https://clinicaltrials.gov/study/NCT02013622 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/02/2014 | https://clinicaltrials.gov/study/NCT02054702 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/03/2015 | https://clinicaltrials.gov/study/NCT02400346 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/03/2015 | https://clinicaltrials.gov/study/NCT02400346 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2011 | https://clinicaltrials.gov/study/NCT01360645 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2011 | https://clinicaltrials.gov/study/NCT01360645 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 04/10/2018 | https://clinicaltrials.gov/study/NCT03737474 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 04/10/2018 | https://clinicaltrials.gov/study/NCT03737474 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | BREXPIPRAZOLE | targetBased | 3 | Recruiting | 10/05/2021 | https://clinicaltrials.gov/study/NCT04569448 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03427892 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03427892 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03427892 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03427892 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03427892 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03427892 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Agitation | BREXPIPRAZOLE | targetBased | 3 | Completed | 16/05/2018 | https://clinicaltrials.gov/study/NCT03548584 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Agitation | BREXPIPRAZOLE | targetBased | 3 | Completed | 16/05/2018 | https://clinicaltrials.gov/study/NCT03548584 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01360632 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02196506 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/10/2019 | https://clinicaltrials.gov/study/NCT04174170 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/10/2019 | https://clinicaltrials.gov/study/NCT04174170 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 17/10/2019 | https://clinicaltrials.gov/study/NCT04124614 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 17/10/2019 | https://clinicaltrials.gov/study/NCT04124614 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Terminated | 01/12/2013 | https://clinicaltrials.gov/study/NCT01987960 | 0.7 | GoF | protect | The study was terminated due to challenges with patient eligibility; the decision to terminate was not based on any safety concerns |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Terminated | 01/12/2013 | https://clinicaltrials.gov/study/NCT01987960 | 0.7 | GoF | protect | The study was terminated due to challenges with patient eligibility; the decision to terminate was not based on any safety concerns |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Withdrawn | 29/08/2022 | https://clinicaltrials.gov/study/NCT05504486 | 1 | GoF | protect | Sponsor strategic decision |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Recruiting | 20/01/2023 | https://clinicaltrials.gov/study/NCT05017311 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Recruiting | 20/01/2023 | https://clinicaltrials.gov/study/NCT05017311 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Recruiting | 20/01/2023 | https://clinicaltrials.gov/study/NCT05017311 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Recruiting | 20/01/2023 | https://clinicaltrials.gov/study/NCT05017311 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Recruiting | 20/01/2023 | https://clinicaltrials.gov/study/NCT05017311 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Recruiting | 20/01/2023 | https://clinicaltrials.gov/study/NCT05017311 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Terminated | 01/12/2013 | https://clinicaltrials.gov/study/NCT01987960 | 0.7 | GoF | protect | The study was terminated due to challenges with patient eligibility; the decision to terminate was not based on any safety concerns |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Terminated | 01/12/2013 | https://clinicaltrials.gov/study/NCT01987960 | 0.7 | GoF | protect | The study was terminated due to challenges with patient eligibility; the decision to terminate was not based on any safety concerns |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Terminated | 01/12/2013 | https://clinicaltrials.gov/study/NCT01987960 | 0.7 | GoF | protect | The study was terminated due to challenges with patient eligibility; the decision to terminate was not based on any safety concerns |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Terminated | 01/12/2013 | https://clinicaltrials.gov/study/NCT01987960 | 0.7 | GoF | protect | The study was terminated due to challenges with patient eligibility; the decision to terminate was not based on any safety concerns |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/10/2019 | https://clinicaltrials.gov/study/NCT04174170 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/10/2019 | https://clinicaltrials.gov/study/NCT04174170 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/10/2019 | https://clinicaltrials.gov/study/NCT04174170 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/10/2019 | https://clinicaltrials.gov/study/NCT04174170 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/10/2019 | https://clinicaltrials.gov/study/NCT04174170 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 30/10/2019 | https://clinicaltrials.gov/study/NCT04174170 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/03/2015 | https://clinicaltrials.gov/study/NCT02400346 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Recruiting | 20/01/2023 | https://clinicaltrials.gov/study/NCT05017311 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Recruiting | 20/01/2023 | https://clinicaltrials.gov/study/NCT05017311 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/04/2021 | https://clinicaltrials.gov/study/NCT04830215 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/04/2021 | https://clinicaltrials.gov/study/NCT04830215 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Withdrawn | 29/08/2022 | https://clinicaltrials.gov/study/NCT05504486 | 1 | GoF | protect | Sponsor strategic decision |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Withdrawn | 29/08/2022 | https://clinicaltrials.gov/study/NCT05504486 | 1 | GoF | protect | Sponsor strategic decision |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Sleep Disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01942733 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | Sleep Disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01942733 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | BREXPIPRAZOLE | targetBased | 3 | Completed | 16/05/2018 | https://clinicaltrials.gov/study/NCT03548584 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | BREXPIPRAZOLE | targetBased | 3 | Completed | 16/05/2018 | https://clinicaltrials.gov/study/NCT03548584 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | BREXPIPRAZOLE | targetBased | 3 | Completed | 16/05/2018 | https://clinicaltrials.gov/study/NCT03548584 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | BREXPIPRAZOLE | targetBased | 3 | Completed | 16/05/2018 | https://clinicaltrials.gov/study/NCT03548584 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | BREXPIPRAZOLE | targetBased | 3 | Completed | 16/05/2018 | https://clinicaltrials.gov/study/NCT03548584 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | BREXPIPRAZOLE | targetBased | 3 | Completed | 16/05/2018 | https://clinicaltrials.gov/study/NCT03548584 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03259555 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 19/09/2017 | https://clinicaltrials.gov/study/NCT03257865 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 24/10/2017 | https://clinicaltrials.gov/study/NCT03287869 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | BREXPIPRAZOLE | targetBased | 3 | Recruiting | 10/05/2021 | https://clinicaltrials.gov/study/NCT04569448 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 01/03/2017 | https://clinicaltrials.gov/study/NCT03427892 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02196506 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02196506 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02196506 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02196506 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01360632 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01360632 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01360632 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01360632 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01360632 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/06/2011 | https://clinicaltrials.gov/study/NCT01360632 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | BREXPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX16 | 1 | LoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/03/2015 | https://clinicaltrials.gov/study/NCT02400346 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | BREXPIPRAZOLE | targetBased | 4 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03149991 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/07/2011 | https://clinicaltrials.gov/study/NCT01360645 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 04/10/2018 | https://clinicaltrials.gov/study/NCT03737474 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | BREXPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX16 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | psychosis | BREXPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX16 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | BREXPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX16 | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | BREXPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX16 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | BREXPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX16 | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | BREXPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX16 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | BREXPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX16 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | BREXPIPRAZOLE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX16 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/rxulti | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/rxulti | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Completed | 27/11/2019 | https://clinicaltrials.gov/study/NCT03874494 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Completed | 27/11/2019 | https://clinicaltrials.gov/study/NCT03874494 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01397786 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2011 | https://clinicaltrials.gov/study/NCT01397786 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 24/10/2017 | https://clinicaltrials.gov/study/NCT03287869 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 24/10/2017 | https://clinicaltrials.gov/study/NCT03287869 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 24/10/2017 | https://clinicaltrials.gov/study/NCT03287869 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 24/10/2017 | https://clinicaltrials.gov/study/NCT03287869 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 19/09/2017 | https://clinicaltrials.gov/study/NCT03257865 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 19/09/2017 | https://clinicaltrials.gov/study/NCT03257865 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 19/09/2017 | https://clinicaltrials.gov/study/NCT03257865 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 19/09/2017 | https://clinicaltrials.gov/study/NCT03257865 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 19/09/2017 | https://clinicaltrials.gov/study/NCT03257865 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 19/09/2017 | https://clinicaltrials.gov/study/NCT03257865 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | BREXPIPRAZOLE | targetBased | 3 | Completed | 16/05/2018 | https://clinicaltrials.gov/study/NCT03548584 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2d301358-6291-4ec1-bd87-37b4ad9bd850 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/rxulti | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/rxulti | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/rxulti | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/rxulti | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/rxulti | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | BREXPIPRAZOLE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/rxulti | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Sleep Disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01942733 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Sleep Disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01942733 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Sleep Disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01942733 | 0.7 | GoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Sleep Disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01942733 | 0.7 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Sleep Disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01942733 | 0.7 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Sleep Disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 01/09/2013 | https://clinicaltrials.gov/study/NCT01942733 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03259555 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 14/09/2017 | https://clinicaltrials.gov/study/NCT03259555 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 19/09/2017 | https://clinicaltrials.gov/study/NCT03257865 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 19/09/2017 | https://clinicaltrials.gov/study/NCT03257865 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 24/10/2017 | https://clinicaltrials.gov/study/NCT03287869 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | bipolar I disorder | BREXPIPRAZOLE | targetBased | 3 | Completed | 24/10/2017 | https://clinicaltrials.gov/study/NCT03287869 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | insomnia | ESMIRTAZAPINE MALEATE | targetBased | 3 | Completed | 07/12/2006 | https://clinicaltrials.gov/study/NCT00610675 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/02/2015 | https://clinicaltrials.gov/study/NCT02146547 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01451736 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Not yet recruiting | 01/08/2012 | https://clinicaltrials.gov/study/NCT01458379 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Unknown status | 01/04/2017 | https://clinicaltrials.gov/study/NCT03080194 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Withdrawn | 01/08/2010 | https://clinicaltrials.gov/study/NCT01193166 | 1 | LoF | protect | This study was stopped due to an internal reconsideration of priorities of the product portfolio. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 18/10/2018 | https://clinicaltrials.gov/study/NCT03713658 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c39e65d7-fa44-4e4c-8b12-a654d3ed0eae | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE PALMITATE | targetBased | 4 | Withdrawn | 01/10/2010 | https://clinicaltrials.gov/study/NCT01211704 | 1 | LoF | protect | lack of funding |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE PALMITATE | targetBased | 4 | Withdrawn | 01/10/2010 | https://clinicaltrials.gov/study/NCT01211704 | 1 | LoF | protect | lack of funding |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE PALMITATE | targetBased | 4 | Withdrawn | 01/10/2010 | https://clinicaltrials.gov/study/NCT01211704 | 1 | LoF | protect | lack of funding |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE PALMITATE | targetBased | 4 | Withdrawn | 01/10/2010 | https://clinicaltrials.gov/study/NCT01211704 | 1 | LoF | protect | lack of funding |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE PALMITATE | targetBased | 4 | Withdrawn | 01/10/2010 | https://clinicaltrials.gov/study/NCT01211704 | 1 | LoF | protect | lack of funding |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | PALIPERIDONE PALMITATE | targetBased | 4 | Withdrawn | 01/10/2010 | https://clinicaltrials.gov/study/NCT01211704 | 1 | LoF | protect | lack of funding |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1af14e42-951d-414d-8564-5d5fce138554 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1af14e42-951d-414d-8564-5d5fce138554 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1af14e42-951d-414d-8564-5d5fce138554 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1af14e42-951d-414d-8564-5d5fce138554 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1af14e42-951d-414d-8564-5d5fce138554 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1af14e42-951d-414d-8564-5d5fce138554 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | PALIPERIDONE PALMITATE | targetBased | 4 | Withdrawn | 01/10/2010 | https://clinicaltrials.gov/study/NCT01211704 | 1 | LoF | protect | lack of funding |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 3 | Completed | 01/09/2010 | https://clinicaltrials.gov/study/NCT01193153 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1af14e42-951d-414d-8564-5d5fce138554 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/03/2011 | https://clinicaltrials.gov/study/NCT01136772 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Unknown status | 01/04/2017 | https://clinicaltrials.gov/study/NCT03080194 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01685931 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01685931 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01685931 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01685931 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01685931 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | PALIPERIDONE PALMITATE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01685931 | 1 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VORTIOXETINE HYDROBROMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1a5b68e2-14d0-419d-9ec6-1ca97145e838 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | major depressive disorder | VORTIOXETINE HYDROBROMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1a5b68e2-14d0-419d-9ec6-1ca97145e838 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VORTIOXETINE HYDROBROMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b0700c9-b417-4c3a-b36f-de461e125bd3 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | unipolar depression | VORTIOXETINE HYDROBROMIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4b0700c9-b417-4c3a-b36f-de461e125bd3 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | PIMAVANSERIN | targetBased | 3 | Terminated | 06/06/2019 | https://clinicaltrials.gov/study/NCT04000009 | 0.7 | LoF | protect | The study was terminated for business reasons and not due to safety concerns. |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | PIMAVANSERIN | targetBased | 3 | Completed | 25/04/2019 | https://clinicaltrials.gov/study/NCT03968159 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | PIMAVANSERIN | targetBased | 3 | Completed | 08/07/2019 | https://clinicaltrials.gov/study/NCT03999918 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PIMAVANSERIN | targetBased | 3 | Active, not recruiting | 01/01/2017 | https://clinicaltrials.gov/study/NCT03121586 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PIMAVANSERIN | targetBased | 3 | Completed | 26/10/2016 | https://clinicaltrials.gov/study/NCT02970292 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | PIMAVANSERIN | targetBased | 3 | Active, not recruiting | 05/08/2020 | https://clinicaltrials.gov/study/NCT04531982 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Hallucinations | PIMAVANSERIN | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1e6bea44-57d6-4bac-9328-46e1ee59f83b | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | PIMAVANSERIN | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1e6bea44-57d6-4bac-9328-46e1ee59f83b | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | PIMAVANSERIN | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AX17 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXEGOL OXALATE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/moventig | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXEGOL OXALATE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/moventig | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXEGOL | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/moventig | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | NALOXEGOL | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/moventig | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 3 | Completed | 15/11/2017 | https://clinicaltrials.gov/study/NCT03345979 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17a8d11b-73b0-4833-a0b4-cf1ef85edefb | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 3 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01626456 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | Completed | 01/12/2015 | https://clinicaltrials.gov/study/NCT02634320 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b18fdfd9-31cd-4a2f-9f1c-ebc70d7a9403 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 3 | Completed | 01/12/2011 | https://clinicaltrials.gov/study/NCT01469039 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | Recruiting | 23/01/2024 | https://clinicaltrials.gov/study/NCT05662306 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 3 | Completed | 01/07/2013 | https://clinicaltrials.gov/study/NCT01895452 | 0.7 | LoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | Completed | 01/12/2015 | https://clinicaltrials.gov/study/NCT02634320 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b18fdfd9-31cd-4a2f-9f1c-ebc70d7a9403 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b18fdfd9-31cd-4a2f-9f1c-ebc70d7a9403 | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17a8d11b-73b0-4833-a0b4-cf1ef85edefb | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17a8d11b-73b0-4833-a0b4-cf1ef85edefb | 1 | GoF | protect | |||
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | Recruiting | 23/01/2024 | https://clinicaltrials.gov/study/NCT05662306 | 1 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | Recruiting | 23/01/2024 | https://clinicaltrials.gov/study/NCT05662306 | 1 | GoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | Recruiting | 23/01/2024 | https://clinicaltrials.gov/study/NCT05662306 | 1 | GoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b18fdfd9-31cd-4a2f-9f1c-ebc70d7a9403 | 1 | GoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b18fdfd9-31cd-4a2f-9f1c-ebc70d7a9403 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b18fdfd9-31cd-4a2f-9f1c-ebc70d7a9403 | 1 | GoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b18fdfd9-31cd-4a2f-9f1c-ebc70d7a9403 | 1 | GoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b18fdfd9-31cd-4a2f-9f1c-ebc70d7a9403 | 1 | GoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ARIPIPRAZOLE LAUROXIL | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b18fdfd9-31cd-4a2f-9f1c-ebc70d7a9403 | 1 | GoF | protect | |||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | depressive disorder | ESKETAMINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/spravato | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | unipolar depression | ESKETAMINE HYDROCHLORIDE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/211243lbl.pdf | 1 | LoF | protect | ||||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | ESKETAMINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d81a6a79-a74a-44b7-822c-0dfa3036eaed | 1 | LoF | protect | ||||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02180659 | 0.7 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | Completed | 22/02/2008 | https://clinicaltrials.gov/study/NCT00604188 | 1 | GoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/sixmo | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00605033 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b086772e-d15a-4d13-b1a2-38bfbde1f18c | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b086772e-d15a-4d13-b1a2-38bfbde1f18c | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b086772e-d15a-4d13-b1a2-38bfbde1f18c | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00605033 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | Completed | 01/03/2008 | https://clinicaltrials.gov/study/NCT00605033 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 3 | Completed | 01/07/2014 | https://clinicaltrials.gov/study/NCT02180659 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | Completed | 22/02/2008 | https://clinicaltrials.gov/study/NCT00604188 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | Completed | 22/02/2008 | https://clinicaltrials.gov/study/NCT00604188 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/sixmo | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | BUPRENORPHINE HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/sixmo | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | OLICERIDINE | targetBased | 4 | Not yet recruiting | 06/06/2024 | https://clinicaltrials.gov/study/NCT06458400 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | pain agnosia | OLICERIDINE | targetBased | 4 | Not yet recruiting | 06/06/2024 | https://clinicaltrials.gov/study/NCT06458400 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Hallucinations | PIMAVANSERIN TARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1e6bea44-57d6-4bac-9328-46e1ee59f83b | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | PIMAVANSERIN TARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=1e6bea44-57d6-4bac-9328-46e1ee59f83b | 1 | LoF | protect | |||
Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP_inhibitors | APP | Amyloid-beta A4 protein, Amyloid-beta precursor protein | Dementia | ADUCANUMAB | pathwayBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06DX03 | 1 | protect | ||||
Primary screen for compounds that activate Alzheimer's amyloid precursor | APP_inhibitors | APP | Amyloid-beta A4 protein, Amyloid-beta precursor protein | Dementia | ADUCANUMAB | pathwayBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06DX03 | 1 | protect | ||||
qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP_inhibitors | APP | Amyloid-beta precursor protein | Dementia | ADUCANUMAB | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N06DX03 | 1 | protect | ||||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | ASENAPINE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=685eaf44-5944-4f38-afba-0a4fc0b3462b | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE | targetBased | 4 | Unknown status | 01/10/2013 | https://clinicaltrials.gov/study/NCT01968161 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01549041 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01460290 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01460290 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01460290 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01460290 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01460290 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01460290 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ASENAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16e1cc9f-7699-49ea-b179-acb65e162304 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ASENAPINE | targetBased | 3 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01395992 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE | targetBased | 3 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00159783 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE | targetBased | 3 | Completed | 14/12/2004 | https://clinicaltrials.gov/study/NCT00159796 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE | targetBased | 3 | Completed | 06/04/2012 | https://clinicaltrials.gov/study/NCT00764478 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01460290 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE | targetBased | 3 | Completed | 16/06/2011 | https://clinicaltrials.gov/study/NCT01244815 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ASENAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH05 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ASENAPINE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00281320 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ASENAPINE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00281320 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH05 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH05 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH05 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH05 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH05 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AH05 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16e1cc9f-7699-49ea-b179-acb65e162304 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16e1cc9f-7699-49ea-b179-acb65e162304 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16e1cc9f-7699-49ea-b179-acb65e162304 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16e1cc9f-7699-49ea-b179-acb65e162304 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16e1cc9f-7699-49ea-b179-acb65e162304 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=16e1cc9f-7699-49ea-b179-acb65e162304 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ASENAPINE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2006 | https://clinicaltrials.gov/study/NCT00322595 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329264 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/12/2012 | https://clinicaltrials.gov/study/NCT01727726 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00320268 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00326144 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Unknown status | 01/05/2011 | https://clinicaltrials.gov/study/NCT01357967 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00326105 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT03207438 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00321490 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/12/2005 | https://clinicaltrials.gov/study/NCT00278941 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00306540 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=51927f2e-3d56-4644-a6a8-40e0b9a5b579 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2a74e8a0-b2fd-4d7f-8bf8-72148b1d3ae7 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=473a3ac4-67f4-4782-baa9-7f9bdd8761f4 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | neurotic disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | obsessive-compulsive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00254735 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Borderline personality disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/11/2010 | https://clinicaltrials.gov/study/NCT01213836 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00214578 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00254735 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00254735 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00254735 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00254735 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00254735 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | obsessive-compulsive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2002 | https://clinicaltrials.gov/study/NCT00254735 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=289fdaa7-ba48-406e-b007-40f4a896f0d1 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aaf50e8a-3c8e-4b19-b539-0384a9b1a707 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9d265a9-7491-48e1-a39e-0aaa67294cff | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=636eeb46-f1e2-4e1b-bc6d-55eb09df9b49 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9d2d5c5c-817d-4631-bd81-de66ab4ff81a | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8048ac0a-5d4d-4d00-ab9c-7fcac27f0a60 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6dd0822c-2d6d-4295-a6de-07756e1cbce7 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6dd0822c-2d6d-4295-a6de-07756e1cbce7 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6dd0822c-2d6d-4295-a6de-07756e1cbce7 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6dd0822c-2d6d-4295-a6de-07756e1cbce7 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6dd0822c-2d6d-4295-a6de-07756e1cbce7 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6dd0822c-2d6d-4295-a6de-07756e1cbce7 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar II disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar II disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Dementia | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Unknown status | 01/05/2011 | https://clinicaltrials.gov/study/NCT01357967 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT03207438 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT03207438 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT03207438 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT03207438 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT03207438 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT03207438 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar II disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00306540 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00306540 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00306540 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00306540 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00306540 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/12/2004 | https://clinicaltrials.gov/study/NCT00306540 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00119652 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00675896 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00675896 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00675896 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00675896 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00675896 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00675896 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=51927f2e-3d56-4644-a6a8-40e0b9a5b579 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | unipolar depression | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7e37e999-f225-4d0a-b16d-37ac14ff29da | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | anxiety | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00621647 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00621647 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00621647 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00621647 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00325689 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00206102 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00206102 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00206102 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00206102 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00206102 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00206102 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2a74e8a0-b2fd-4d7f-8bf8-72148b1d3ae7 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2004 | https://clinicaltrials.gov/study/NCT00227305 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2004 | https://clinicaltrials.gov/study/NCT00107731 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/04/2009 | https://clinicaltrials.gov/study/NCT00857818 | 0.7 | LoF | protect | Slow Accrual |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=0f131f23-80dd-4a42-893a-b7d86cd0e037 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=55c1bce9-9d05-4621-839d-a98b8d862692 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9cde17b6-2452-4227-8a19-61acb57cff4f | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e2d7800d-930a-49fe-9450-0e96833d44c2 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=94dfc588-1fd9-4435-93ec-c6dd4700aef5 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8df82f5a-aa0e-4f8c-bae1-2f32ede3d7b6 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=760c11f5-b3d2-4b24-94e9-d907a7448557 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329446 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329264 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329264 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329264 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329264 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329264 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | generalized anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00329264 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00449397 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | neurotic disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/09/2003 | https://clinicaltrials.gov/study/NCT00206102 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/04/2009 | https://clinicaltrials.gov/study/NCT00857818 | 0.7 | LoF | protect | Slow Accrual |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00325689 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2005 | https://clinicaltrials.gov/study/NCT00206141 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00119652 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | depressive disorder | QUETIAPINE FUMARATE | targetBased | 4 | Completed | 01/04/2007 | https://clinicaltrials.gov/study/NCT00675896 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00449397 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00449397 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00449397 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00449397 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00449397 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/07/2003 | https://clinicaltrials.gov/study/NCT00449397 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | anxiety | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/08/2007 | https://clinicaltrials.gov/study/NCT00534599 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Dementia | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03517f29-f270-4350-a57a-fbe1967b0096 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=45c4c3a4-3acc-413e-9746-4816d513fac6 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/03/2003 | https://clinicaltrials.gov/study/NCT00124059 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | alcohol dependence | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/01/2006 | https://clinicaltrials.gov/study/NCT00114686 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/09/2002 | https://clinicaltrials.gov/study/NCT00621647 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | QUETIAPINE FUMARATE | targetBased | 3 | Terminated | 01/05/2006 | https://clinicaltrials.gov/study/NCT00315900 | 0.7 | LoF | protect | Investigator closed study and left VAMC. |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6173e1ce-0a85-40b0-99f0-1a6d78e67198 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9fe6267a-c7b3-41e8-9006-a43014716acb | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9fe6267a-c7b3-41e8-9006-a43014716acb | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9fe6267a-c7b3-41e8-9006-a43014716acb | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9fe6267a-c7b3-41e8-9006-a43014716acb | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9fe6267a-c7b3-41e8-9006-a43014716acb | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | QUETIAPINE FUMARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9fe6267a-c7b3-41e8-9006-a43014716acb | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00773162 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00773162 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00773162 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00773162 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00773162 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | social anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00773162 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Borderline personality disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/05/2005 | https://clinicaltrials.gov/study/NCT00122070 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | social anxiety disorder | QUETIAPINE FUMARATE | targetBased | 3 | Completed | 01/10/2008 | https://clinicaltrials.gov/study/NCT00773162 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | DASOTRALINE | targetBased | 3 | Completed | 29/02/2016 | https://clinicaltrials.gov/study/NCT02684279 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | eating disorder | DASOTRALINE | targetBased | 3 | Completed | 31/03/2017 | https://clinicaltrials.gov/study/NCT03107026 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DASOTRALINE | targetBased | 3 | Completed | 31/07/2017 | https://clinicaltrials.gov/study/NCT03231800 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DASOTRALINE | targetBased | 3 | Completed | 01/06/2014 | https://clinicaltrials.gov/study/NCT02160262 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DASOTRALINE | targetBased | 3 | Completed | 30/06/2015 | https://clinicaltrials.gov/study/NCT02457819 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DASOTRALINE | targetBased | 3 | Completed | 30/04/2016 | https://clinicaltrials.gov/study/NCT02734693 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DASOTRALINE | targetBased | 3 | Completed | 01/12/2014 | https://clinicaltrials.gov/study/NCT02276209 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | CENTANAFADINE | targetBased | 3 | Completed | 02/02/2022 | https://clinicaltrials.gov/study/NCT05257265 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | CENTANAFADINE | targetBased | 3 | Recruiting | 24/02/2022 | https://clinicaltrials.gov/study/NCT05279313 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | CENTANAFADINE | targetBased | 3 | Completed | 14/02/2019 | https://clinicaltrials.gov/study/NCT03605849 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | CENTANAFADINE | targetBased | 3 | Completed | 16/01/2019 | https://clinicaltrials.gov/study/NCT03605680 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | CENTANAFADINE | targetBased | 3 | Completed | 16/01/2019 | https://clinicaltrials.gov/study/NCT03605836 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | CENTANAFADINE | targetBased | 3 | Recruiting | 11/07/2022 | https://clinicaltrials.gov/study/NCT05428033 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | LUMATEPERONE | targetBased | 3 | Recruiting | 02/05/2023 | https://clinicaltrials.gov/study/NCT05850689 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 30/09/2021 | https://clinicaltrials.gov/study/NCT05061706 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 30/07/2021 | https://clinicaltrials.gov/study/NCT04985942 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | LUMATEPERONE | targetBased | 3 | Enrolling by invitation | 08/10/2021 | https://clinicaltrials.gov/study/NCT05061719 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LUMATEPERONE | targetBased | 3 | Completed | 01/06/2015 | https://clinicaltrials.gov/study/NCT02469155 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LUMATEPERONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=db730b06-6351-47fd-8183-e61e61bbead5 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LUMATEPERONE | targetBased | 3 | Active, not recruiting | 08/07/2021 | https://clinicaltrials.gov/study/NCT04959032 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LUMATEPERONE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/209500s000lbl.pdf | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | LUMATEPERONE | targetBased | 3 | Completed | 01/11/2014 | https://clinicaltrials.gov/study/NCT02282761 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 15/12/2015 | https://clinicaltrials.gov/study/NCT02600494 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 15/12/2015 | https://clinicaltrials.gov/study/NCT02600494 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 15/12/2015 | https://clinicaltrials.gov/study/NCT02600494 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 15/12/2015 | https://clinicaltrials.gov/study/NCT02600494 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 30/09/2021 | https://clinicaltrials.gov/study/NCT05061706 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 30/09/2021 | https://clinicaltrials.gov/study/NCT05061706 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 30/09/2021 | https://clinicaltrials.gov/study/NCT05061706 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 30/09/2021 | https://clinicaltrials.gov/study/NCT05061706 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LUMATEPERONE | targetBased | 3 | Not yet recruiting | 01/07/2024 | https://clinicaltrials.gov/study/NCT06462612 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 07/03/2016 | https://clinicaltrials.gov/study/NCT02600507 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 15/12/2015 | https://clinicaltrials.gov/study/NCT02600494 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/02/2020 | https://clinicaltrials.gov/study/NCT04285515 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LUMATEPERONE | targetBased | 3 | Recruiting | 01/04/2024 | https://clinicaltrials.gov/study/NCT06372964 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LUMATEPERONE | targetBased | 3 | Completed | 27/11/2017 | https://clinicaltrials.gov/study/NCT03249376 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | LUMATEPERONE | targetBased | 3 | Recruiting | 01/06/2024 | https://clinicaltrials.gov/study/NCT06462586 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | LUMATEPERONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD10 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | LUMATEPERONE | targetBased | 4 | Terminated | 11/05/2023 | https://clinicaltrials.gov/study/NCT05890768 | 1 | LoF | protect | PI was unable to meet 1 year recruitment goal |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | LUMATEPERONE | targetBased | 4 | Terminated | 11/05/2023 | https://clinicaltrials.gov/study/NCT05890768 | 1 | LoF | protect | PI was unable to meet 1 year recruitment goal |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | LUMATEPERONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD10 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | LUMATEPERONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD10 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | LUMATEPERONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD10 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | LUMATEPERONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD10 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | LUMATEPERONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD10 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | LUMATEPERONE | targetBased | 4 | https://www.whocc.no/atc_ddd_index/?code=N05AD10 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LUMATEPERONE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=db730b06-6351-47fd-8183-e61e61bbead5 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | LUMATEPERONE | targetBased | 4 | Recruiting | 02/04/2024 | https://clinicaltrials.gov/study/NCT06174116 | 1 | LoF | protect | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Completed | 02/11/2016 | https://clinicaltrials.gov/study/NCT02943577 | 0.7 | GoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Completed | 01/11/2016 | https://clinicaltrials.gov/study/NCT02943564 | 0.7 | GoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Completed | 13/11/2016 | https://clinicaltrials.gov/study/NCT02951988 | 0.7 | GoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Terminated | 30/10/2018 | https://clinicaltrials.gov/study/NCT03675776 | 0.7 | GoF | protect | Business decision to stop the program. | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Terminated | 02/08/2018 | https://clinicaltrials.gov/study/NCT03614156 | 0.7 | GoF | protect | Business decision to stop the program. | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Withdrawn | 01/07/2019 | https://clinicaltrials.gov/study/NCT03855865 | 0.7 | GoF | protect | Business decision to stop the program. | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Terminated | 15/06/2018 | https://clinicaltrials.gov/study/NCT03560518 | 0.7 | GoF | protect | Business decision to stop the program. | |
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Completed | 03/02/2017 | https://clinicaltrials.gov/study/NCT03002077 | 0.7 | GoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Completed | 15/10/2016 | https://clinicaltrials.gov/study/NCT02932943 | 0.7 | GoF | protect | ||
uHTS identification of small molecule modulators of NR3A | GRIN3A | GRIN3A | major depressive disorder | RAPASTINEL | targetBased | 3 | Terminated | 23/08/2018 | https://clinicaltrials.gov/study/NCT03668600 | 0.7 | GoF | protect | Business decision to stop the program | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | DEXTROAMPHETAMINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE SULFATE | targetBased | 3 | Completed | 10/03/2005 | https://clinicaltrials.gov/study/NCT00152035 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE SULFATE | targetBased | 3 | Completed | 27/01/2005 | https://clinicaltrials.gov/study/NCT00150579 | 0.7 | protect | ||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE SULFATE | targetBased | 3 | Completed | 25/04/2005 | https://clinicaltrials.gov/study/NCT00152022 | 0.7 | protect | ||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | major depressive disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | post-traumatic stress disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | Unknown status | 01/10/2013 | https://clinicaltrials.gov/study/NCT01968161 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01549041 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00174265 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | mental or behavioural disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | major depressive disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/10/2012 | https://clinicaltrials.gov/study/NCT01670019 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | post-traumatic stress disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/06/2012 | https://clinicaltrials.gov/study/NCT01587118 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01395992 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar I disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03c696e9-0e6b-4e5c-be0a-41416f8019be | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/10/2011 | https://clinicaltrials.gov/study/NCT01460290 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/12/2011 | https://clinicaltrials.gov/study/NCT01396291 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 14/12/2004 | https://clinicaltrials.gov/study/NCT00159796 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/07/2005 | https://clinicaltrials.gov/study/NCT00159783 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 07/01/2005 | https://clinicaltrials.gov/study/NCT00143182 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | mental or behavioural disorder | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/01/2009 | https://clinicaltrials.gov/study/NCT00806234 | 1 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | psychosis | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00281320 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 04/09/2003 | https://clinicaltrials.gov/study/NCT00212784 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/09/2004 | https://clinicaltrials.gov/study/NCT00212771 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00281320 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00281320 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00281320 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00281320 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00281320 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | psychosis | ASENAPINE MALEATE | targetBased | 3 | Completed | 01/02/2006 | https://clinicaltrials.gov/study/NCT00281320 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar I disorder | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=86a40942-8d6b-478c-995f-3c346b197463 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | ASENAPINE MALEATE | targetBased | 4 | Completed | 01/04/2012 | https://clinicaltrials.gov/study/NCT01400113 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5429f134-839f-4ffc-9944-55f51238def8 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ASENAPINE MALEATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=17209c32-56eb-4f84-954d-aed7b7a1b18d | 1 | LoF | protect | |||
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | LEMBOREXANT | targetBased | 4 | Completed | 24/03/2021 | https://clinicaltrials.gov/study/NCT04742699 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | LEMBOREXANT | targetBased | 4 | Completed | 24/03/2021 | https://clinicaltrials.gov/study/NCT04742699 | 1 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | LEMBOREXANT | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7074cb65-77b3-45d2-8e8d-da8dc0f70bfd | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | LEMBOREXANT | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7074cb65-77b3-45d2-8e8d-da8dc0f70bfd | 1 | LoF | protect | |||
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | LEMBOREXANT | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212028s000lbl.pdf | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | LEMBOREXANT | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212028s000lbl.pdf | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | LEMBOREXANT | targetBased | 3 | Completed | 31/05/2016 | https://clinicaltrials.gov/study/NCT02783729 | 0.7 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | alcohol dependence | LEMBOREXANT | targetBased | 3 | Completed | 09/02/2023 | https://clinicaltrials.gov/study/NCT05458609 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | alcohol dependence | LEMBOREXANT | targetBased | 3 | Completed | 09/02/2023 | https://clinicaltrials.gov/study/NCT05458609 | 0.7 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | Sleep Disorder | LEMBOREXANT | targetBased | 3 | Completed | 06/11/2020 | https://clinicaltrials.gov/study/NCT04549168 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | Sleep Disorder | LEMBOREXANT | targetBased | 3 | Completed | 06/11/2020 | https://clinicaltrials.gov/study/NCT04549168 | 0.7 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | Sleep Disorder | LEMBOREXANT | targetBased | 4 | Recruiting | 10/03/2022 | https://clinicaltrials.gov/study/NCT05344443 | 1 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | Sleep Disorder | LEMBOREXANT | targetBased | 4 | Recruiting | 10/03/2022 | https://clinicaltrials.gov/study/NCT05344443 | 1 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | HYDROCODONE BITARTRATE | targetBased | 4 | Completed | 30/01/2018 | https://clinicaltrials.gov/study/NCT03457116 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=901d4115-f71a-4681-bd0e-c9b691151b78 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b3c9e-b7e4-455b-9482-61714aea2b14 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b3c9e-b7e4-455b-9482-61714aea2b14 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6ccfbd98-7750-4955-a654-ec104fb666f9 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6ccfbd98-7750-4955-a654-ec104fb666f9 | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9e5daeac-8573-48e9-877f-c08701255c5b | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9e5daeac-8573-48e9-877f-c08701255c5b | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6ccfbd98-7750-4955-a654-ec104fb666f9 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=901d4115-f71a-4681-bd0e-c9b691151b78 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=016b3c9e-b7e4-455b-9482-61714aea2b14 | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=470df63a-5c0f-42df-9023-a330a901153e | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9e5daeac-8573-48e9-877f-c08701255c5b | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | HYDROCODONE BITARTRATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=25f400d9-1d6e-4d38-8f0d-98d471eba73b | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | HYDROCODONE BITARTRATE | targetBased | 4 | Completed | 30/01/2018 | https://clinicaltrials.gov/study/NCT03457116 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | HYDROCODONE BITARTRATE | targetBased | 4 | Completed | 30/01/2018 | https://clinicaltrials.gov/study/NCT03457116 | 1 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | OLANZAPINE PAMOATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00320489 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00320489 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00320489 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00320489 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f9a73185-88de-4d7b-b3c0-bbf231483241 | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | OLANZAPINE PAMOATE | targetBased | 3 | Completed | 01/04/2006 | https://clinicaltrials.gov/study/NCT00320489 | 0.7 | LoF | protect | |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ADRB2 | Beta-2 adrenergic receptor | nicotine dependence | FORMOTEROL FUMARATE | targetBased | 3 | Completed | 01/05/2017 | https://clinicaltrials.gov/study/NCT03104634 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | ZIPRASIDONE MESYLATE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00723606 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE MESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5c03ca62-5dd5-4cf5-abc7-b0c2873503dd | 1 | LoF | protect | |||
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE MESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5c03ca62-5dd5-4cf5-abc7-b0c2873503dd | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE MESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5c03ca62-5dd5-4cf5-abc7-b0c2873503dd | 1 | LoF | protect | |||
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE MESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5c03ca62-5dd5-4cf5-abc7-b0c2873503dd | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE MESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5c03ca62-5dd5-4cf5-abc7-b0c2873503dd | 1 | LoF | protect | |||
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | bipolar disorder | ZIPRASIDONE MESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5c03ca62-5dd5-4cf5-abc7-b0c2873503dd | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | bipolar disorder | ZIPRASIDONE MESYLATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5c03ca62-5dd5-4cf5-abc7-b0c2873503dd | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE MESYLATE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00723606 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE MESYLATE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00723606 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE MESYLATE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00723606 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE MESYLATE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00723606 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE MESYLATE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00723606 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | ZIPRASIDONE MESYLATE | targetBased | 3 | Completed | 01/09/2008 | https://clinicaltrials.gov/study/NCT00723606 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | narcolepsy-cataplexy syndrome | DEXTROAMPHETAMINE SACCHARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | DEXTROAMPHETAMINE SACCHARATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=ffd56d70-d884-43be-a994-6e70a10e823e | 1 | protect | ||||
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | delirium | LIRAGLUTIDE | targetBased | 3 | Not yet recruiting | 30/04/2024 | https://clinicaltrials.gov/study/NCT06361238 | 0.7 | GoF | protect | |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | delirium | LIRAGLUTIDE | targetBased | 3 | Not yet recruiting | 30/04/2024 | https://clinicaltrials.gov/study/NCT06361238 | 0.7 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | delirium | LIRAGLUTIDE | targetBased | 3 | Not yet recruiting | 30/04/2024 | https://clinicaltrials.gov/study/NCT06361238 | 0.7 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | major depressive disorder | LIRAGLUTIDE | targetBased | 3 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02423824 | 0.7 | GoF | protect | |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | major depressive disorder | LIRAGLUTIDE | targetBased | 3 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02423824 | 0.7 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | major depressive disorder | LIRAGLUTIDE | targetBased | 3 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02423824 | 0.7 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | binge eating | LIRAGLUTIDE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01739049 | 1 | GoF | protect | |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | binge eating | LIRAGLUTIDE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01739049 | 1 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | binge eating | LIRAGLUTIDE | targetBased | 4 | Completed | 01/11/2012 | https://clinicaltrials.gov/study/NCT01739049 | 1 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | eating disorder | LIRAGLUTIDE | targetBased | 3 | Terminated | 29/09/2017 | https://clinicaltrials.gov/study/NCT03279731 | 0.7 | GoF | protect | The study was not meeting recruitment goals. |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | eating disorder | LIRAGLUTIDE | targetBased | 3 | Terminated | 29/09/2017 | https://clinicaltrials.gov/study/NCT03279731 | 0.7 | GoF | protect | The study was not meeting recruitment goals. |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | eating disorder | LIRAGLUTIDE | targetBased | 3 | Terminated | 29/09/2017 | https://clinicaltrials.gov/study/NCT03279731 | 0.7 | GoF | protect | The study was not meeting recruitment goals. |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | bipolar disorder | LIRAGLUTIDE | targetBased | 3 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02423824 | 0.7 | GoF | protect | |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | bipolar disorder | LIRAGLUTIDE | targetBased | 3 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02423824 | 0.7 | GoF | protect | |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | GLP1R | Glucagon-like peptide 1 receptor , Glucagon-like peptide-1 receptor | bipolar disorder | LIRAGLUTIDE | targetBased | 3 | Completed | 01/05/2015 | https://clinicaltrials.gov/study/NCT02423824 | 0.7 | GoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=010905f9-3bcb-4b50-9fe8-a3ad0010f14c | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | drug dependence | CODEINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=010905f9-3bcb-4b50-9fe8-a3ad0010f14c | 1 | GoF | protect | |||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | drug dependence | CODEINE SULFATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=010905f9-3bcb-4b50-9fe8-a3ad0010f14c | 1 | GoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e52d40f2-b658-4bc6-8a0c-74a340b762d8 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e2eed126-cb82-42b1-9b48-9cbeb6873b50 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=34893e69-ed5c-4929-bb15-fd8780d5034f | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8397a841-f240-4767-9dcd-781e6d3f7c7f | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7ce7f23c-f58b-4b8b-a31a-47bd4e792345 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=153e747c-861d-44c4-aef6-6c49f53ca34a | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c72c2366-7b40-4cd9-845d-4b3983e6141a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=89dc5e08-67c7-448a-95e7-56bb77e62cce | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8397a841-f240-4767-9dcd-781e6d3f7c7f | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8397a841-f240-4767-9dcd-781e6d3f7c7f | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8397a841-f240-4767-9dcd-781e6d3f7c7f | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=909259a3-7627-4d1e-91d3-3363b3493599 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=909259a3-7627-4d1e-91d3-3363b3493599 | 1 | LoF | protect | |||
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=909259a3-7627-4d1e-91d3-3363b3493599 | 1 | LoF | protect | |||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | HTR2A | 5-hydroxytryptamine receptor 2A | Agitation | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c72c2366-7b40-4cd9-845d-4b3983e6141a | 1 | LoF | protect | |||
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00159081 | 1 | LoF | protect | |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00159081 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00159081 | 1 | LoF | protect | |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00159081 | 1 | LoF | protect | |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00159081 | 1 | LoF | protect | |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | DRD2 | Dopaminereceptor2 | schizophrenia | HALOPERIDOL LACTATE | targetBased | 4 | Completed | 01/11/2000 | https://clinicaltrials.gov/study/NCT00159081 | 1 | LoF | protect | |
qHTS of D3 Dopamine Receptor Antagonist: qHTS | D3_antagonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Agonist: qHTS | D3_agonists | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
qHTS of D3 Dopamine Receptor Potentiators: qHTS | D3_PAMs | DRD3 | Dopaminereceptor3 | schizoaffective disorder | HALOPERIDOL LACTATE | targetBased | 3 | Completed | 01/07/2006 | https://clinicaltrials.gov/study/NCT00797277 | 0.7 | LoF | protect | |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | AVPR1A | Vasopressin V1a receptor | autism spectrum disorder | BALOVAPTAN | targetBased | 3 | Terminated | 08/08/2018 | https://clinicaltrials.gov/study/NCT03504917 | 0.35 | LoF | protect | A futility analysis assessed that the study is highly unlikely to meet the pre-defined primary objective of the study. No new safety concerns were identified. |
Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R | MC4R | MC4R | Melanocortin receptor 4 | mental or behavioural disorder | BREMELANOTIDE ACETATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9146ae05-918b-483e-b86d-933485ce36eb | 1 | GoF | protect | |||
TRFRET-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): antagonists of MC4R | MC4R | MC4R | Melanocortin receptor 4 | mental or behavioural disorder | BREMELANOTIDE ACETATE | targetBased | 4 | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9146ae05-918b-483e-b86d-933485ce36eb | 1 | GoF | protect | |||
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT | targetBased | 3 | Recruiting | 28/08/2023 | https://clinicaltrials.gov/study/NCT06010693 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT | targetBased | 3 | Recruiting | 28/08/2023 | https://clinicaltrials.gov/study/NCT06010693 | 0.7 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/214985s000lbl.pdf | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/214985s000lbl.pdf | 1 | LoF | protect | |||
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/quviviq | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/quviviq | 1 | LoF | protect | |||
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT | targetBased | 3 | Completed | 29/05/2018 | https://clinicaltrials.gov/study/NCT03575104 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT | targetBased | 3 | Completed | 29/05/2018 | https://clinicaltrials.gov/study/NCT03575104 | 0.7 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | SERDEXMETHYLPHENIDATE CHLORIDE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/212994s000lbl.pdf | 1 | LoF | protect | |||
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | SERDEXMETHYLPHENIDATE | targetBased | 4 | Recruiting | 14/09/2023 | https://clinicaltrials.gov/study/NCT06000501 | 1 | LoF | protect | |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | SLC6A3 | Sodium-dependent dopamine transporter | attention deficit hyperactivity disorder | SERDEXMETHYLPHENIDATE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/212994s000lbl.pdf | 1 | LoF | protect | |||
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT HYDROCHLORIDE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/214985s000lbl.pdf | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT HYDROCHLORIDE | targetBased | 4 | https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/214985s000lbl.pdf | 1 | LoF | protect | |||
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/quviviq | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | DARIDOREXANT HYDROCHLORIDE | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/quviviq | 1 | LoF | protect | |||
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Enrolling by invitation | 31/03/2023 | https://clinicaltrials.gov/study/NCT05741528 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Enrolling by invitation | 31/03/2023 | https://clinicaltrials.gov/study/NCT05741528 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Terminated | 16/05/2022 | https://clinicaltrials.gov/study/NCT05359081 | 0.7 | GoF | protect | Due to company business strategy |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Terminated | 16/05/2022 | https://clinicaltrials.gov/study/NCT05359081 | 0.7 | GoF | protect | Due to company business strategy |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Completed | 30/09/2019 | https://clinicaltrials.gov/study/NCT04092686 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Completed | 30/09/2019 | https://clinicaltrials.gov/study/NCT04092686 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Terminated | 04/10/2019 | https://clinicaltrials.gov/study/NCT04109950 | 0.7 | GoF | protect | Study terminated early, main goals achieved |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Terminated | 04/10/2019 | https://clinicaltrials.gov/study/NCT04109950 | 0.7 | GoF | protect | Study terminated early, main goals achieved |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Completed | 19/12/2022 | https://clinicaltrials.gov/study/NCT05628103 | 0.7 | GoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | TAAR1 | Trace amine-associated receptor 1 | schizophrenia | ULOTARONT | targetBased | 3 | Completed | 19/12/2022 | https://clinicaltrials.gov/study/NCT05628103 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Terminated | 16/05/2022 | https://clinicaltrials.gov/study/NCT05359081 | 0.7 | GoF | protect | Due to company business strategy |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Terminated | 16/05/2022 | https://clinicaltrials.gov/study/NCT05359081 | 0.7 | GoF | protect | Due to company business strategy |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Terminated | 04/10/2019 | https://clinicaltrials.gov/study/NCT04109950 | 0.7 | GoF | protect | Study terminated early, main goals achieved |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Terminated | 04/10/2019 | https://clinicaltrials.gov/study/NCT04109950 | 0.7 | GoF | protect | Study terminated early, main goals achieved |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Enrolling by invitation | 31/03/2023 | https://clinicaltrials.gov/study/NCT05741528 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Enrolling by invitation | 31/03/2023 | https://clinicaltrials.gov/study/NCT05741528 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Completed | 19/12/2022 | https://clinicaltrials.gov/study/NCT05628103 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Completed | 19/12/2022 | https://clinicaltrials.gov/study/NCT05628103 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Completed | 30/09/2019 | https://clinicaltrials.gov/study/NCT04092686 | 0.7 | GoF | protect | |
Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | HTR1A | 5-hydroxytryptamine receptor 1A | schizophrenia | ULOTARONT | targetBased | 3 | Completed | 30/09/2019 | https://clinicaltrials.gov/study/NCT04092686 | 0.7 | GoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | ORN-0829 HYDRATE | targetBased | 3 | Completed | 30/08/2022 | https://clinicaltrials.gov/study/NCT05453136 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | ORN-0829 HYDRATE | targetBased | 3 | Completed | 30/08/2022 | https://clinicaltrials.gov/study/NCT05453136 | 0.7 | LoF | protect | |
FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | ORN-0829 HYDRATE | targetBased | 3 | Completed | 11/10/2022 | https://clinicaltrials.gov/study/NCT05461352 | 0.7 | LoF | protect | |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | HCRTR1 | Orexin/Hypocretin receptor type 1 | insomnia | ORN-0829 HYDRATE | targetBased | 3 | Completed | 11/10/2022 | https://clinicaltrials.gov/study/NCT05461352 | 0.7 | LoF | protect | |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | opioid dependence | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/nyxoid | 1 | LoF | protect | ||||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/nyxoid | 1 | LoF | protect | ||||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | opioid dependence | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/nyxoid | 1 | LoF | protect | ||||
Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/selincro | 1 | LoF | protect | ||||
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | OPRM1 | Mu-type opioid receptor | alcohol dependence | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/selincro | 1 | LoF | protect | ||||
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | OPRK1 | Kappa-type opioid receptor | alcohol dependence | targetBased | 4 | https://www.ema.europa.eu/en/medicines/human/EPAR/selincro | 1 | GoF | protect |