drugset / Trial / NCT04267393

Safety and Effectiveness of BMS-986263 in Adults With Compensated Cirrhosis (Liver Disease) From Nonalcoholic Steatohepatitis (NASH)

NCT04267393

Phase 2 Terminated 124 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this randomized study is to assess safety and effectiveness of BMS-986263 in adults with compensated cirrhosis (chronic liver disease) from nonalcoholic steatohepatitis (fatty liver disease) (NASH).

Timeline

Start
2021-03-17
Primary completion
2023-08-16
Completion
2024-02-09

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-986263 Small interfering RNA (siRNA)