drugset / Trial / NCT01716585

A Study to Evaluate Chronic Hepatitis C Infection

NCT01716585 ↗

Phase 3 Completed 636 enrolled AbbVie
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of ABT-450, ritonavir and ABT-267 (ABT-450/r/ABT-267; ABT-267 also known as ombitasvir) and ABT-333 (also known as dasabuvir) co-administered with ribavirin (RBV) in hepatitis C virus genotype 1 infected treatment-naïve adults.

Timeline

Start
2012-11
Primary completion
2013-10
Completion
2014-10

Outcome

Met primary endpoint

paper The rate of sustained virologic response in group A was 96.2% (95% confidence interval, 94.5 to 97.9), which was superior to the historical control rate. PMID 24720703 ↗

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 —