Overview

Ombitasvir/ABT-450 (Paritaprevir)/Ritonavir With Dasabuvir and Ribavirin (RBV) in Treatment Naive and Treatment Experienced Genotype 1a Hepatitis C Virus Infected Adults

Status:
Completed
Trial end date:
2016-12-01
Target enrollment:
0
Participant gender:
All
Summary
A study to evaluate immune restoration following removal of viral antigen in non-cirrhotic hepatitis C virus (HCV) genotype (GT) 1a treatment-naïve and pegylated-interferon (pegIFN)/ribavirin (RBV) treatment-experienced adults receiving treatment with ombitasvir/paritaprevir/ritonavir and dasabuvir coadministered with ribavirin (RBV) for 12 weeks.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
AbbVie
Treatments:
Ribavirin
Ritonavir
Criteria
Inclusion Criteria:

1. Screening laboratory result indicating hepatitis C viral (HCV) genotype (GT) 1a
infection.

2. Chronic HCV infection.

3. Participants must be non-cirrhotic.

4. Participants must be treatment-naïve or have documentation that they were adherent to
prior pegIFN/RBV combination therapy and meet the criteria of prior
pegylated-interferon (pegIFN)/ribavirin (RBV) treatment failure.

5. Participants must meet specific human leukocyte antigen (HLA) allele requirements.

Exclusion Criteria:

1. Women who are pregnant or breastfeeding.

2. Positive test result for hepatitis B surface antigen (HBsAg) or anti-human
immunodeficiency virus antibody (HIV Ab) positive immunoassay.

3. Clinically significant abnormalities or co-morbidities, other than HCV infection, that
make the subject unsuitable for this study or treatment.

4. Current enrollment in another interventional clinical study, previous enrollment in
this study, prior or current use of any investigational or commercially available
anti-HCV agents other than pegIFN or RBV (including previous exposure to paritaprevir,
ombitasvir, or dasabuvir), or receipt of any investigational product within 6 weeks
prior to study drug administration.

5. History of solid organ transplant.

6. Screening laboratory analysis that shows abnormal results.