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Last Updated: November 25, 2024

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CLINICAL TRIALS PROFILE FOR CAPLYTA


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All Clinical Trials for caplyta

Trial ID Title Status Sponsor Phase Start Date Summary
NCT05356013 ↗ Caplyta in Borderline Personality Disorder Not yet recruiting Intra-Cellular Therapies, Inc. Phase 2 2022-07-01 The primary objective of the proposed study is to evaluate the safety and efficacy of Caplyta (lumateperone) in adults with borderline personality disorder (BPD). Sixty subjects with BPD will be randomized in a 1:1 fashion to either Caplyta (42mg/day) or matching placebo for 8 weeks of active treatment. The hypothesis to be tested is that Caplyta will result in greater rates of reduction in symptoms of BPD compared to placebo (improvement in symptoms will be indicated by lower scores on established outcome measures of BPD symptoms that have been used in prior studies).
NCT05356013 ↗ Caplyta in Borderline Personality Disorder Not yet recruiting University of Chicago Phase 2 2022-07-01 The primary objective of the proposed study is to evaluate the safety and efficacy of Caplyta (lumateperone) in adults with borderline personality disorder (BPD). Sixty subjects with BPD will be randomized in a 1:1 fashion to either Caplyta (42mg/day) or matching placebo for 8 weeks of active treatment. The hypothesis to be tested is that Caplyta will result in greater rates of reduction in symptoms of BPD compared to placebo (improvement in symptoms will be indicated by lower scores on established outcome measures of BPD symptoms that have been used in prior studies).
NCT05890768 ↗ Relationship Between Efficacy of Lumateperone and Brain Glutamate and Dopamine Recruiting University of New Mexico Phase 4 2023-05-11 This study will examine the differential relationships between antipsychotic efficacy and changes in dopaminergic and glutamatergic brain metabolism in lumateperone and risperidone treated early psychosis patients. Baseline glutamate and dopamine brain scans, and symptom severity measures will be collected, followed by repeated measures at 6 weeks. Half of the early psychosis patients will be treated with lumateperone, half with risperidone. Healthy control subejcts will also be examined once.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for caplyta

Condition Name

Condition Name for caplyta
Intervention Trials
Psychosis 1
Schizo Affective Disorder 1
Schizophrenia 1
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Condition MeSH

Condition MeSH for caplyta
Intervention Trials
Psychotic Disorders 2
Mental Disorders 1
Personality Disorders 1
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Clinical Trial Locations for caplyta

Trials by Country

Trials by Country for caplyta
Location Trials
United States 2
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Trials by US State

Trials by US State for caplyta
Location Trials
Massachusetts 1
New Mexico 1
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Clinical Trial Progress for caplyta

Clinical Trial Phase

Clinical Trial Phase for caplyta
Clinical Trial Phase Trials
Phase 4 2
Phase 2 1
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Clinical Trial Status

Clinical Trial Status for caplyta
Clinical Trial Phase Trials
Recruiting 2
Not yet recruiting 1
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Clinical Trial Sponsors for caplyta

Sponsor Name

Sponsor Name for caplyta
Sponsor Trials
Intra-Cellular Therapies, Inc. 2
University of Chicago 1
University of New Mexico 1
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Sponsor Type

Sponsor Type for caplyta
Sponsor Trials
Other 3
Industry 2
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