drugset / Trial / NCT02123654
UNITY 3: A Japanese Phase 3 Study of a Daclatasvir/Asunaprevir/BMS-791325 in Subjects With Genotype 1 Chronic Hepatitis C
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Asunaprevir | Small molecule | 100 mg | Oral |
| Subject | DCV 3DAA | Unknown | — | Oral |
| Comparator | Daclatasvir | Small molecule | 60 mg | Oral |