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NOT YET RECRUITING
NCT07747389
PHASE3

A Study of Lumateperone Versus Placebo in Participants With Major Depressive Disorder

Sponsor: Intra-Cellular Therapies, Inc.

View on ClinicalTrials.gov

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

Interventions

DRUG

Lumateperone

Participants will receive lumateperone orally.

DRUG

Placebo

Participants will receive placebo orally.