drugset / Trial / NCT02498015

A Phase IV Trial of Paritaprevir/Ritonavir, Ombitasvir, Dasabuvir for Chronic Hepatitis C Genotype 1 Virus Infection

NCT02498015

Phase 4 Completed 87 enrolled Kirby Institute
Non-randomizedSingle-groupOpen-labelTreatment

Summary

A total of 100 people with chronic HCV and recent injection drug use or recipients of opioid substitution therapy will be enrolled in 5 countries and 21 study sites. Participants with genotype 1a infection or cirrhosis will receive 12 weeks of open-label paritaprevir/ritonavir/ombitasvir and dasabuvir ("3D"), and twice-daily ribavirin. Participants with genotype 1b infection without cirrhosis will receive 12 weeks of open-label "3D". The study consists of a screening phase (6 weeks), treatment phase (12 weeks) and follow-up phase (96 weeks) to evaluate treatment response and reinfection.

Timeline

Start
2016-08
Primary completion
2017-08
Completion
2019-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribavirin Small molecule 1000 mg
Subject Ritonavir Other / unclassified 50 mg
Subject dasabuvir Small molecule 250 mg
Subject ombitasvir Small molecule 12.5 mg
Subject paritaprevir Small molecule 75 mg