drugset / Trial / NCT02939989

Efficacy and Safety of Glecaprevir (ABT-493)/Pibrentasvir (ABT 530) (GLE/PIB) in Combination With Sofosbuvir and Ribavirin in Participants With Hepatitis C Virus Who Did Not Respond to Treatment in a Previous AbbVie Clinical Study

NCT02939989

Phase 3 Completed 33 enrolled AbbVie
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to evaluate the efficacy and safety of co-administration of glecaprevir (ABT-493)/pibrentasvir (ABT 530) plus sofosbuvir (SOF) plus ribavirin (RBV) in hepatitis C virus (HCV) genotype (GT) 1 - 6-infected participants (including non-cirrhotic, or cirrhotic with compensated cirrhosis participants) who had experienced virologic failure in an AbbVie parent clinical study.

Timeline

Start
2016-11-21
Primary completion
2021-05-07
Completion
2021-07-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Glecaprevir/Pibrentasvir Unknown 120 mg Oral
Subject Glecaprevir/Pibrentasvir Unknown 300 mg Oral
Subject Ribavirin Small molecule 600 mg Oral
Subject Ribavirin Small molecule 1200 mg Oral
Subject Sofosbuvir Small molecule 400 mg Oral