drugset / Trial / NCT02442284

A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With or Without Ribavirin in US Veterans With Genotype 1 Chronic Hepatitis C Virus Infection

NCT02442284

Phase 3 Completed 99 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of ombitasvir/paritaprevir/ritonavir and dasabuvir with or without ribavirin in US veterans with genotype 1 chronic hepatitis C virus infection.

Timeline

Start
2015-05-13
Primary completion
2016-08-22
Completion
2016-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribavirin Small molecule 1000 mg
Subject Ribavirin Small molecule 1200 mg
Subject Ritonavir Other / unclassified 100 mg
Subject dasabuvir Small molecule 250 mg
Subject ombitasvir Small molecule 25 mg
Subject paritaprevir Small molecule 150 mg