RecruitingPhase 2NCT07459647

A Long-Term Open-Label Study of ML-007C-MA in Adults With Schizophrenia

An Open-Label Study to Assess the Long-Term Safety, Tolerability, and Effectiveness of ML-007C-MA in Adult Participants With Schizophrenia


Sponsor

MapLight Therapeutics

Enrollment

500 participants

Start Date

Mar 31, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

ML-007C-MA-212 is a 52-week open-label study designed to evaluate the long-term safety, tolerability, and effectiveness of ML-007C-MA in participants with schizophrenia who have recently completed an antecedent study (ML-007C-MA-211) or enroll directly (De Novo Cohort).


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called ML-007C-MA for people with schizophrenia. The study is currently recruiting participants at 5 locations. People eligible for this study include aged 18 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGML-007C-MA

ML-007C-MA dosed as 210/3 mg BID


Locations(5)

Clinical Site

Lemon Grove, California, United States

Clinical Site

Miami Lakes, Florida, United States

Clinical Site

Chicago, Illinois, United States

Clinical Site

Staten Island, New York, United States

Clinical Site

DeSoto, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07459647


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