drugset / Trial / NCT02636595

The Efficacy and Safety of ABT-493/ABT-530 in Adults With Chronic Hepatitis C Virus Genotype 4, 5, or 6 Infection (ENDURANCE-4)

NCT02636595

Phase 3 Completed 121 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the effect of response to treatment by evaluating the percentage of subjects achieving a 12-week sustained virologic response (SVR12) after 12 weeks of treatment with ABT-493/ABT-530 and to evaluate the safety of the regimen in participants with chronic hepatitis C virus (HCV) genotype (GT) 4, 5, or 6 infection.

Timeline

Start
2015-11
Primary completion
2016-10
Completion
2017-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject glecaprevir Other / unclassified 300 mg Oral
Subject pibrentasvir Other / unclassified 120 mg Oral