drugset / Trial / NCT01701401

Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination (FDC) With and Without Ribavirin for the Treatment of HCV

NCT01701401 ↗

Phase 3 Completed 870 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and antiviral efficacy of ledipasvir (LDV)/sofosbuvir (SOF) fixed-dose combination (FDC) tablets with or without ribavirin (RBV) administered for 12 and 24 weeks in treatment-naive subjects with chronic genotype 1 HCV infection.

Timeline

Start
2012-09
Primary completion
2014-03
Completion
2014-04

Outcome

Met primary endpoint

registry analysis (superiority or other test); LDV/SOF 12 Weeks; p <0.001; Binomial test; NCT01701401 ↗

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