drugset / Trial / NCT02243280

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-administration of ABT-493 and ABT-530 With and Without Ribavirin in Subjects With HCV Genotype 1, 4, 5, and 6 Infection

NCT02243280

Phase 2 Completed 174 enrolled AbbVie
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this Phase 2, open-label, 2-part, multicenter study was to evaluate the efficacy, safety, and pharmacokinetics of co-administration of ABT-493 and ABT-530 with and without ribavirin (RBV) at different doses in chronic Hepatitis C virus (HCV) Genotype 1 (GT1), Genotype 4 (GT4), Genotype 5 (GT5), and Genotype 6 (GT6) infection with compensated cirrhosis (GT1 only) or without cirrhosis (GT1, GT4, GT5, or GT6). Although RBV was initially planned in the protocol, it was not administered in any of the study arms.

Timeline

Start
2014-08
Primary completion
2016-02
Completion
2016-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject glecaprevir Other / unclassified 200 mg Oral
Subject glecaprevir Other / unclassified 300 mg Oral
Subject pibrentasvir Other / unclassified 40 mg Oral
Subject pibrentasvir Other / unclassified 120 mg Oral