drugset / Trial / NCT01051414

An Anti-viral Combination Study With Japanese Hepatitis C Infection (HCV) Subject

NCT01051414

Phase 2 Completed 43 enrolled Bristol-Myers Squibb
NaSingle-groupOpen-labelTreatment

Summary

To assess the efficacy and safety profile of co-administration of BMS-790052 and BMS-650032 for 24 weeks treatment.

Timeline

Start
2010-04
Primary completion
2011-09
Completion
2012-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Asunaprevir Small molecule 1200 mg Oral
Subject Daclatasvir Small molecule 60 mg Oral