drugset / Trial / NCT01767116

A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1b Infection

NCT01767116 ↗

Phase 3 Completed 419 enrolled AbbVie
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety and antiviral activity of ABT-450/ritonavir/ABT-267 (ABT-450/r/ABT-267; ABT-450 also known as paritaprevir; ABT-267 also known as ombitasvir) and ABT-333 (also known as dasabuvir) with and without ribavirin (RBV) in patients with chronic hepatitis C virus genotype 1b (HCV GT1b) infection without cirrhosis.

Timeline

Start
2012-12
Primary completion
2013-12
Completion
2014-08

Outcome

Met primary endpoint

release “The PEARL-III study met its primary and secondary endpoints.” enanta.com ↗

Drugs

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