At a glance
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An Open-Label, Multicenter Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Combination With Sofosbuvir and Ribavirin in Chronic Hepatitis C (HCV) Infected Subjects Who Have Experienced Virologic Failure in AbbVie HCV Clinical Studies (MAGELLAN-3)
In Brief
A Phase 3 clinical trial evaluating Sofosbuvir, Glecaprevir/Pibrentasvir, and 1 other intervention for Hepatitis C Virus Infection. Completed, enrolled 33 participants across 26 sites in 12 countries.
Detailed 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.
Study Details
Timeline
Interventions
Tablet for oral administration
Coformulated tablet for oral administration
Tablet for oral administration