ITI-007-505 | Clinical Research Studies Listing

Recruiting

65 years or below

All

Phase N/A

1 Location

Brief description of study

This is an international, multicenter, randomized, double-blind, placebo-controlled, parallel-group, fixed-dose study in patients with a primary diagnosis of MDD to evaluate the efficacy of lumateperone 42 mg administered once daily compared with placebo as adjunctive treatment to antidepressant therapy

Eligibility of study

You may be eligible for this study if you meet the following criteria:

Conditions: Medical Research
Age: 65 years or below
Gender: All

TBD

Updated on 17 Jun 2025. Study ID: 23-0816

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