drugset / Trial / NCT02582632

A Study to Evaluate Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir in Treatment-Naïve Hepatitis C Virus Genotype 1b-Infected Adults

NCT02582632

Phase 3 Completed 166 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety and efficacy of ombitasvir/paritaprevir/ ritonavir and dasabuvir administered for 8 weeks in treatment-naïve participants with genotype 1b (GT1b) hepatitis C virus (HCV).

Timeline

Start
2015-11-24
Primary completion
2016-08-24
Completion
2016-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Ritonavir Other / unclassified 100 mg
Subject dasabuvir Small molecule 250 mg
Subject ombitasvir Small molecule 25 mg
Subject paritaprevir Small molecule 150 mg