drugset / Trial / NCT02378961
Safety and Efficacy of Voxilaprevir Plus Sofosbuvir/Velpatasvir Fixed Dose Combination in Adults With Chronic Non-Genotype 1 HCV Infection
Non-randomizedSequentialOpen-labelTreatment
Summary
The primary objectives of the study are to evaluate the safety, tolerability, and efficacy of voxilaprevir (VOX) plus sofosbuvir/velpatasvir (SOF/VEL) fixed dose combination (FDC) in adults with chronic non genotype 1 hepatitis C virus (HCV) infection.
Timeline
- Start
- 2015-02-16
- Primary completion
- 2015-09-21
- Completion
- 2016-01-26
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Sofosbuvir | Small molecule | 400 mg | Oral |
| Subject | VOX | Unknown | 100 mg | Oral |
| Subject | velpatasvir | Other / unclassified | 100 mg | Oral |