drugset / Trial / NCT02378961

Safety and Efficacy of Voxilaprevir Plus Sofosbuvir/Velpatasvir Fixed Dose Combination in Adults With Chronic Non-Genotype 1 HCV Infection

NCT02378961

Phase 2 Completed 128 enrolled Gilead Sciences
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

EvaluationDrugModalityDoseRoute
Subject Sofosbuvir Small molecule 400 mg Oral
Subject VOX Unknown 100 mg Oral
Subject velpatasvir Other / unclassified 100 mg Oral