drugset / Trial / NCT02413593

Safety and Efficacy of Ledipasvir/Sofosbuvir (LDV/SOF) Fixed Dose Combination Tablet With Ribavirin for 12 Weeks in Treatment-naive Adults With Chronic HCV Genotype 3 Infection

NCT02413593 ↗

Phase 2 Completed 111 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the antiviral efficacy, safety, and tolerability of ledipasvir/sofosbuvir (LDV/SOF) fixed dose combination (FDC) plus ribavirin (RBV) in treatment-naive adults with chronic genotype 3 hepatitis C virus (HCV) infection.

Timeline

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

Outcome

Met primary endpoint

release “achieved a sustained virologic response 12 weeks after completing therapy (SVR12)” gilead.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ledipasvir/Sofosbuvir Unknown 90 mg Oral
Subject Ledipasvir/Sofosbuvir Unknown 400 mg Oral
Subject Ribavirin Small molecule 1000 mg Oral
Subject Ribavirin Small molecule 1200 mg Oral