drugset / Trial / NCT02217475

Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Participants With Liver Fibrosis

NCT02217475 ↗

Phase 2 Completed 289 enrolled Tobira Therapeutics, Inc.
RandomizedCrossoverTriple-blindTreatment

Summary

The purpose of this study is to determine whether cenicriviroc is effective and safe in the treatment of nonalcoholic steatohepatitis (NASH) in adult participants with liver fibrosis.

Timeline

Start
2014-09-18
Primary completion
2016-06-30
Completion
2017-06-22

Outcome

Missed primary endpoint

registry analysis (superiority test); Placebo vs CVC 150 mg; p = 0.5194; Odds Ratio (OR) 0.816 (95% CI 0.439 to 1.516); Regression, Logistic NCT02217475 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cenicriviroc Small molecule 150 mg Oral