drugset / Trial / NCT00971308

Multiple Dose Study In Treatment Naive Subjects Infected With Hepatitis C Virus

NCT00971308 ↗

Phase 1 Completed 37 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the antiviral effect following three days of dosing with BMS-824393 in chronically genotype subtype 1a and 1b Hepatitis C virus (HCV) infected subjects.

Timeline

Start
2009-10
Primary completion
2010-08
Completion
2010-08

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-824393 Unknown 1 mg Oral
Subject BMS-824393 Unknown 10 mg Oral
Subject BMS-824393 Unknown 50 mg Oral
Subject BMS-824393 Unknown 100 mg Oral