drugset / Trial / NCT02613871

Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination in Adults With Chronic HCV and HBV Coinfection

NCT02613871 ↗

Phase 3 Completed 111 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

Summary

The primary objectives of this study are to determine the antiviral efficacy, safety, and tolerability of ledipasvir/sofosbuvir (LDV/SOF) fixed-dose combination (FDC) in adults with chronic genotype 1 or 2 HCV infection who are coinfected with HBV in Taiwan.

Timeline

Start
2015-12-22
Primary completion
2017-01-04
Completion
2018-11-07

Outcome

Met primary endpoint

paper All 111 patients (100%) achieved a sustained virologic response. PMID 29174546 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ledipasvir/Sofosbuvir Unknown 90 mg Oral
Subject Ledipasvir/Sofosbuvir Unknown 400 mg Oral