drugset / Trial / NCT01455090

Study to Determine the Effectiveness and Safety of a Three Drug Antiviral Combination Therapy to Treat Hepatitis C Virus (HCV) Infected Patients Not Previously Treated With Currently Available Medications

NCT01455090

Phase 2 Completed 320 enrolled Bristol-Myers Squibb
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to estimate the rate of sustained virologic response (SVR) SVR12, where SVR12 is defined as HCV RNA \< LOQ (detectable or undetectable) 12 weeks post-treatment in Genotype 1 \& Genotype 4 treatment naive patients, and Genotype (GT1) infected patients who are prior null responders to pegIFN/ribavirin

Timeline

Start
2011-11-30
Primary completion
2014-03-31
Completion
2015-07-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Asunaprevir Small molecule 200 mg
Subject Beclabuvir Small molecule 75 mg
Subject Beclabuvir Small molecule 150 mg
Subject Daclatasvir Small molecule 30 mg
Subject Daclatasvir Small molecule 60 mg
Subject Ribavirin Small molecule 1000 mg Oral
Subject Ribavirin Small molecule 1200 mg Oral