Clinical Trials Directory

Trials / Completed

CompletedNCT01767116

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

A Randomized, Double-blind, Controlled Study to Evaluate the Efficacy and Safety of the Combination of ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 With and Without Ribavirin (RBV) in Treatment-Naive Adults With Genotype 1b Chronic Hepatitis C Virus (HCV) Infection (PEARL-III)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
419 (actual)
Sponsor
AbbVie (prior sponsor, Abbott) · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

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.

Detailed description

A randomized, double-blind, multicenter study to evaluate the safety and antiviral activity of the combination of ABT-450/ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 with and without ribavirin (RBV) in treatment-naïve, noncirrhotic participants with chronic hepatitis C virus genotype 1b (HCV GT1b) infection.

Conditions

Interventions

TypeNameDescription
DRUGABT-450/r/ABT-267, ABT-333Tablet; ABT-450 coformulated with ritonavir and ABT-267, ABT-333 tablet
DRUGRibavirinCapsule
DRUGPlacebo for ribavirinCapsule

Timeline

Start date
2012-12-01
Primary completion
2013-12-01
Completion
2014-08-01
First posted
2013-01-14
Last updated
2021-07-12
Results posted
2015-01-06

Source: ClinicalTrials.gov record NCT01767116. Inclusion in this directory is not an endorsement.