drugset / Trial / NCT01858766

Safety and Efficacy of Sofosbuvir + Velpatasvir With or Without Ribavirin in Treatment-Naive Adults With Chronic HCV Infection

NCT01858766

Phase 2 Completed 379 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objectives of this study are to evaluate the antiviral efficacy, safety, and tolerability of sofosbuvir (SOF) + velpatasvir (VEL; GS-5816) with or without ribavirin (RBV) in treatment-naive adults with chronic genotype (GT) 1, 2, 3, 4, 5, or 6 hepatitis C virus (HCV) infection.

Timeline

Start
2013-04
Primary completion
2014-05
Completion
2014-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribavirin Small molecule 1000 mg Oral
Subject Ribavirin Small molecule 1200 mg Oral
Subject Sofosbuvir Small molecule 400 mg Oral
Subject velpatasvir Other / unclassified 25 mg Oral
Subject velpatasvir Other / unclassified 100 mg Oral