drugset / Trial / NCT03053050

Safety and Efficacy of Selonsertib in Adults With Nonalcoholic Steatohepatitis (NASH) and Bridging (F3) Fibrosis

NCT03053050 ↗

Phase 3 Terminated 808 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate whether selonsertib (SEL; GS-4997) can cause fibrosis regression and reduce progression to cirrhosis and associated complications in adults with NASH and bridging (F3) fibrosis.

Timeline

Start
2017-02-13
Primary completion
2019-06-19
Completion
2019-06-19

Outcome

Missed primary endpoint

Stopped: “This study was terminated early due to lack of efficacy based on the results of the Week 48 analysis as prespecified in the clinical study protocol.”

paper Neither trial met the primary efficacy endpoint. PMID 32147362 ↗

registry analysis (superiority test); SEL 18 mg vs Placebo; p = 0.4941; Percentage Difference -2.1 (95% CI -8.3 to 4.0) NCT03053050 ↗

registry analysis (superiority test); SEL 6 mg vs Placebo; p = 0.9321; Percentage Difference -0.3 (95% CI -6.6 to 6.0) NCT03053050 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Selonsertib Small molecule 6 mg Oral
Subject Selonsertib Small molecule 18 mg Oral