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

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ProScience Research Group

Culver City, CA United States
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Synergy Clinical Center

National City, CA United States
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Behavioral Clinical Research, Inc

North Miami, FL United States
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Research Centers of America, LLC

Oakland Park, FL United States
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Pillar Clinical Research LLC

Richardson, TX United States
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Recruitment Status: Open


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