drugset / Trial / NCT02480712

Efficacy and Safety of Sofosbuvir/Velpatasvir Fixed Dose Combination for 12 Weeks in Adults With Chronic Hepatitis C Virus (HCV) and Human Immunodeficiency Virus (HIV)-1 Coinfection

NCT02480712

Phase 3 Completed 107 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

Summary

The primary objectives of this study are to evaluate the efficacy, safety and tolerability of treatment with sofosbuvir/velpatasvir (SOF/VEL) for 12 weeks in participants with chronic HCV infection who were coinfected with HIV-1.

Timeline

Start
2015-07-01
Primary completion
2016-04-29
Completion
2016-06-22

Publications

Drugs

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