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Clinical Trial Summary

This phase 2, double blind, placebo-controlled, randomized study is to assess the safety and efficacy of miricorilant in obese adult with schizophrenia treated with antipsychotic medications.


Clinical Trial Description

This is a randomized, double-blind, placebo-controlled study that will assess the safety, efficacy, and PK of miricorilant in obese patients with schizophrenia or bipolar disorder who are currently taking oral or injectable atypical antipsychotic medication. Patients who meet the criteria for the Study CORT118335-876 will be randomized on Day 1 to receive 600 mg miricorilant or placebo for 12 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03818256
Study type Interventional
Source Corcept Therapeutics
Contact
Status Completed
Phase Phase 2
Start date October 31, 2019
Completion date December 31, 2022

See also
  Status Clinical Trial Phase
Completed NCT04524403 - Study Evaluating the Safety, Efficacy, and Pharmacokinetics of Miricorilant in Obese Adult Patients With Schizophrenia While Taking Antipsychotic Medications (GRATITUDE II) Phase 2