drugset / Trial / NCT01359644

Study to Determine the Safety and Effectiveness of Antiviral Combination Therapy to Treat Hepatitis C Virus (HCV) in Patients Who Have Previously Not Received the Standard of Care

NCT01359644

Phase 2 Completed 350 enrolled Bristol-Myers Squibb Pharmasset · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to determine whether therapy with the combination of PSI-7977 and daclatasvir (BMS-790052) with or without ribavirin is effective in treating hepatitis C virus (HCV) infection when given for 12 or 24 weeks as measured by sustained virologic response with undetectable HCV RNA 12 weeks post treatment

Timeline

Start
2011-06
Primary completion
2013-01
Completion
2013-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Daclatasvir Small molecule 60 mg Oral
Subject Ribavirin Small molecule 200 mg Oral
Subject Sofosbuvir Small molecule 400 mg Oral