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Recruiting Phase 3 NCT06462612

Study of Lumateperone in the Treatment of Patients With Bipolar Mania

Trial Parameters

Condition Bipolar Disorder, Manic
Sponsor Intra-Cellular Therapies, Inc.
Study Type INTERVENTIONAL
Phase Phase 3
Enrollment 350
Sex ALL
Min Age 18 Years
Max Age 75 Years
Start Date 2024-07-17
Completion 2026-05
Interventions
LumateperonePlacebo

Brief Summary

This is a multicenter, randomized, double-blind, placebo-controlled, study in the acute treatment of patients with a diagnosis of bipolar I disorder with manic episodes or manic episodes with mixed features (bipolar mania), with or without psychotic symptoms, according to criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM 5).

Eligibility Criteria

Inclusion Criteria: 1. Able to provide written informed consent before the initiation of any study specific procedures; 2. Male or female inpatient, between the ages of 18 and 75 years, inclusive; 3. Meets the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM 5) criteria for bipolar I disorder with a current episode of mania or mania with mixed features with or without psychotic symptoms, as confirmed by a trained and Sponsor-approved rater using the modified Structured Clinical Interview for DSM-5, Clinical Trials Version (SCID-5-CT); 4. YMRS total score ≥ 20 and a score of at least 4 on two of the following YMRS items: irritability, speech, content, and disruptive/aggressive behavior at Screening and Baseline; 5. Hospitalized voluntarily before Screening or admitted to inpatient unit at Visit 1 with a primary diagnosis of mania but not \> 14 days before Screening. Hospital admission must be a result of the current manic episode. Exclusion Criteria: 1. Has a curr

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