Trials / Completed
CompletedNCT01833533
A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1a 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-Naïve Adults With Genotype 1a Chronic Hepatitis C Virus (HCV) Infection (PEARL-IV)
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 305 (actual)
- Sponsor
- AbbVie · 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 1a (HCV GT1a) infection without cirrhosis.
Detailed description
A randomized, double-blind, placebo-controlled, 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-naive, noncirrhotic participants with chronic hepatitis C virus genotype 1a (HCV GT1a) infection.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | ABT-450/r/ABT-267, ABT-333 | Tablet; ABT-450 coformulated with ritonavir and ABT-267, ABT-333 tablet |
| DRUG | Ribavirin | Capsule |
| DRUG | Placebo for Ribavirin | Capsule |
Timeline
- Start date
- 2013-03-01
- Primary completion
- 2013-12-01
- Completion
- 2014-09-01
- First posted
- 2013-04-17
- Last updated
- 2021-07-12
- Results posted
- 2015-01-06
Source: ClinicalTrials.gov record NCT01833533. Inclusion in this directory is not an endorsement.