drugset / Trial / NCT01628692

Study of Daclatasvir (BMS-790052) and Simeprevir (TMC435) in Patients With Genotype 1 Chronic Hepatitis C Virus

NCT01628692

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and efficacy of daclatasvir and simeprevir with and without ribavirin for genotype 1 chronic hepatitis C virus infection in patients who are treatment-naive or null responders to previous pegylated interferon/ribavirin therapy.

Timeline

Start
2012-07
Primary completion
2013-08
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Daclatasvir Small molecule 30 mg Oral
Subject Ribavirin Small molecule 500 mg Oral
Subject Ribavirin Small molecule 600 mg Oral
Subject Simeprevir Small molecule 150 mg Oral