drugset / Trial / NCT02123654

UNITY 3: A Japanese Phase 3 Study of a Daclatasvir/Asunaprevir/BMS-791325 in Subjects With Genotype 1 Chronic Hepatitis C

NCT02123654

Phase 3 Completed 297 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to demonstrate that the proportion of treatment-naive non-cirrhotic subjects with Genotype (GT)-1b treated with Daclatasvir (DCV)/Asunaprevir (ASV)/BMS-791325 who achieve Sustained Virologic response (SVR12), defined as Hepatitis C virus (HCV) RNA \< LOQ target detected or target not detected (LOQ TD/TND) at follow-up Week 12, is significantly higher than SVR12 of current Standard of Care (SOC).

Timeline

Start
2014-04
Primary completion
2015-01
Completion
2015-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Asunaprevir Small molecule 100 mg Oral
Subject DCV 3DAA Unknown Oral
Comparator Daclatasvir Small molecule 60 mg Oral