drugset / Trial / NCT01851330

Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination ± Ribavirin for the Treatment of HCV (ION-3)

NCT01851330 ↗

Phase 3 Completed 647 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is to evaluate the safety, tolerability, and antiviral efficacy of ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) with or without ribavirin (RBV) administered for 8 or 12 weeks in treatment-naive participants with chronic genotype 1 HCV infection.

Timeline

Start
2013-05
Primary completion
2013-12
Completion
2014-03

Outcome

Met primary endpoint

paper these results indicated noninferiority of the 8-week ledipasvir-sofosbuvir regimen, on the basis of a noninferiority margin of 12 percentage points. PMID 24720702 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject LDV/SOF Unknown 90 mg Oral
Subject LDV/SOF Unknown 400 mg Oral
Subject Ribavirin Small molecule 1000 mg Oral
Subject Ribavirin Small molecule 1200 mg Oral