Last updated on September 2018

Study to Evaluate Efficacy and Safety of Roluperidone (MIN-101) in Adult Patients With Negative Symptoms of Schizophrenia

Brief description of study

MIN-101C07 is a multicenter, multinational, randomized, double-blind, placebo-controlled, parallel-group study to evaluate the efficacy and safety of roluperidone in adult schizophrenia patients.The primary objective is to evaluate the efficacy of 2 fixed doses of roluperidone compared to placebo in improving the negative symptoms of schizophrenia over 12 weeks of double-blind treatment as measured by the change in Positive and Negative Syndrome Scale (PANSS) Marder negative symptoms factor score (NSFS) over 12 weeks.

Clinical Study Identifier: NCT03397134

Find a site near you

Start Over

ProScience Research Group

Culver City, CA United States
  Connect »

Synergy Clinical Center

National City, CA United States
  Connect »

Behavioral Clinical Research, Inc

North Miami, FL United States
  Connect »

Research Centers of America, LLC

Oakland Park, FL United States
  Connect »

Pillar Clinical Research LLC

Richardson, TX United States
  Connect »

Recruitment Status: Open

Brief Description Eligibility Contact Research Team

Receive Emails About New Clinical Trials!

Sign up for our FREE service to receive email notifications when clinical trials are posted in the medical category of interest to you.