drugset / Trial / NCT02607735

Safety and Efficacy of Sofosbuvir/Velpatasvir/Voxilaprevir in Adults With Chronic HCV Infection Who Have Previously Received Treatment With Direct-Acting Antiviral Therapy

NCT02607735 ↗

Phase 3 Completed 416 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objectives of this study are to evaluate the safety and efficacy of treatment with sofosbuvir/velpatasvir/voxilaprevir (SOF/VEL/VOX) in adults with chronic hepatitis C virus (HCV) infection who have previously received treatment with direct-acting antiviral therapy. Participants randomized to placebo may be eligible for deferred treatment with active SOF/VEL/VOX.

Timeline

Start
2015-11-11
Primary completion
2016-10-10
Completion
2017-06-21

Outcome

Met primary endpoint

registry NUMBER SOF/VEL/VOX (Primary Study): 96.2 (93.1 to 98.8) percentage of participants NCT02607735 ↗

registry analysis (superiority test); SOF/VEL/VOX (Primary Study); p <0.001; 2-sided exact 1-sample binomial test NCT02607735 ↗

release “The POLARIS-1, POLARIS-3 and POLARIS-4 studies met their respective pre-specified primary endpoints for the patients receiving SOF/VEL/VOX.” gilead.com ↗

Publications

Drugs

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