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A Study of Lumateperone Versus Placebo in Participants With Major Depressive Disorder
Sponsor: Intra-Cellular Therapies, Inc.
Summary
The purpose of the study is to assess how well each dose of lumateperone (Dose 1 and 2) works when given alone as compared to placebo in participants with major depressive disorder (MDD; a medical condition characterized by a persistent feeling of deep sadness, hopelessness, and a loss of interest in activities for a prolonged period of time and interfere with ability to function).
Official title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Assess the Efficacy and Safety of Fixed Doses of Lumateperone Administered as Monotherapy in Participants With Major Depressive Disorder and an Open-label Long-term Extension Treatment With Lumateperone
Key Details
Gender
All
Age Range
18 Years - 74 Years
Study Type
INTERVENTIONAL
Enrollment
585
Start Date
2026-10-20
Completion Date
2029-09-20
Last Updated
2026-08-05
Healthy Volunteers
No
Conditions
Interventions
Lumateperone
Participants will receive lumateperone orally.
Placebo
Participants will receive placebo orally.