drugset / Trial / NCT02170727

A Phase 3 Study of a Daclatasvir/Asunaprevir/BMS-791325 Fixed Dose Combination (FDC) in Subjects With Chronic Hepatitis C Genotype 1

NCT02170727

Phase 3 Completed 199 enrolled Bristol-Myers Squibb
NaSingle-groupOpen-labelTreatment

Summary

To demonstrate the effectiveness of Daclatasvir (DCV) 3 Direct Acting Antivirals (DAA) fixed dose combination in Genotype 1 Chronic Hepatitis C subjects.

Timeline

Start
2014-06-26
Primary completion
2015-06-12
Completion
2015-09-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Asunaprevir Small molecule 200 mg Oral
Subject Beclabuvir Small molecule 75 mg Oral
Subject Daclatasvir Small molecule 30 mg Oral