drugset / Trial / NCT03212521

Efficacy and Safety of 8-weeks of Glecaprevir/Pibrentasvir in Treatment-Naïve Adults With HCV Genotype 1-6 and Aspartate Aminotransferase to Platelet Ratio Index (APRI) ≤1

NCT03212521

Phase 3 Completed 230 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

A study to evaluate the efficacy and safety of glecaprevir(GLE)/pibrentasvir(PIB) in treatment-naïve participants with chronic hepatitis C virus (HCV) genotypes 1-6 infection and with an aspartate aminotransferase to platelet ratio index (APRI) of less than or equal to 1.

Timeline

Start
2017-08-07
Primary completion
2018-08-13
Completion
2018-08-13

Drugs

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