drugset / Trial / NCT01628692
Study of Daclatasvir (BMS-790052) and Simeprevir (TMC435) in Patients With Genotype 1 Chronic Hepatitis C Virus
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |