drugset / Trial / NCT02243293

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-Administration of ABT-493 and ABT-530 With and Without RBV in Subjects With Chronic Hepatitis C Virus (HCV) Genotypes 2, 3, 4, 5 or 6 Infection

NCT02243293

Phase 2/3 Completed 694 enrolled AbbVie
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this phase 2/3, open-label, multipart, multicenter study was to evaluate the efficacy, and safety of co-administration of ABT-493 and ABT-530 with and without ribavirin (RBV) in chronic HCV genotype 2 (GT2-), genotype 3 (GT3-), genotype 4 (GT4), genotype 5 (GT5-), or genotype 6 (GT6-) infected participants with or without cirrhosis.

Timeline

Start
2014-09-19
Primary completion
2016-10-25
Completion
2017-02-23

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject ABT-493/ABT-530 Unknown Oral
Subject Ribavirin Small molecule 800 mg
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 80 mg Oral
Subject pibrentasvir Other / unclassified 120 mg Oral