drugset / Trial / NCT03067129

A Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Glecaprevir/Pibrentasvir in Pediatric Subjects With Genotypes 1-6 Chronic Hepatitis C Virus (HCV) Infection

NCT03067129

Phase 2/3 Completed 129 enrolled AbbVie
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The objectives of this study are to assess the pharmacokinetics, safety, and efficacy of glecaprevir/pibrentasvir adult formulation in adolescents ages 12 to 17 years and a pediatric formulation of glecaprevir and pibrentasvir in children ages 3 to \< 12 years.

Timeline

Start
2017-03-20
Primary completion
2020-05-21
Completion
2022-09-12

Drugs

EvaluationDrugModalityDoseRoute
Subject glecaprevir Other / unclassified 150 mg Oral
Subject glecaprevir Other / unclassified 200 mg Oral
Subject glecaprevir Other / unclassified 250 mg Oral
Subject glecaprevir Other / unclassified 300 mg Oral
Subject pibrentasvir Other / unclassified 60 mg Oral
Subject pibrentasvir Other / unclassified 80 mg Oral
Subject pibrentasvir Other / unclassified 100 mg Oral
Subject pibrentasvir Other / unclassified 120 mg Oral