drugset / Trial / NCT02378935

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

NCT02378935

Phase 2 Completed 205 enrolled Gilead Sciences
Non-randomizedSequentialOpen-labelTreatment

Summary

This 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) ± ribavirin (RBV) in adults with chronic genotype 1 hepatitis C virus (HCV) infection.

Timeline

Start
2015-02-17
Primary completion
2016-02-01
Completion
2016-04-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribavirin Small molecule 1000 mg Oral
Subject Ribavirin Small molecule 1200 mg Oral
Subject Sofosbuvir Small molecule 400 mg Oral
Subject Voxilaprevir Small molecule 100 mg Oral
Subject velpatasvir Other / unclassified 100 mg Oral