drugset / Trial / NCT02220998

Comparison of Sofosbuvir/Velpatasvir Fixed Dose Combination for 12 Weeks With Sofosbuvir and Ribavirin for 12 Weeks in Adults With Chronic Genotype 2 HCV Infection

NCT02220998

Phase 3 Completed 269 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objectives of this study are to evaluate the efficacy, safety, and tolerability of treatment with sofosbuvir/velpatasvir (SOF/VEL) fixed-dose combination (FDC) for 12 weeks compared to treatment with sofosbuvir (SOF) plus ribavirin (RBV) for 12 weeks in participants with chronic genotype 2 hepatitis C virus (HCV) infection.

Timeline

Start
2014-09
Primary completion
2015-07
Completion
2015-09

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribavirin Small molecule 1000 mg Oral
Subject Ribavirin Small molecule 1200 mg Oral
Subject SOF/VEL Unknown 100 mg Oral
Subject SOF/VEL Unknown 400 mg Oral
Subject Sofosbuvir Small molecule 400 mg Oral