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Phase 2 N=129 Treatment

A Study to Evaluate Chronic Hepatitis C Infection in Adult Transplant Recipients

Chronic Hepatitis C Infection

Enrolled (actual)
129
Serious AEs
7.8%
Results posted
Nov 2017
Primary outcome: Primary: Percentage of Participants With Sustained Virologic Response 12 Weeks Post-treatment (SVR12) — 97.1; 96.3; 100; 100 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
ombitasvir/paritaprevir/ritonavir and dasabuvir (Drug); ombitasvir/paritaprevir/ritonavir (Drug); ribavirin (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
AbbVie
Primary completion
Nov 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants With Sustained Virologic Response 12 Weeks Post-treatment (SVR12)
97.1; 96.3; 100; 100; 100; 95.5
SECONDARY
Percentage of Participants With Sustained Virologic Response 24 Weeks Post-treatment (SVR24)
97.1; 96.3; 100; 100; 100; 95.5
SECONDARY
Percentage of Participants With On-treatment Virologic Failure
0; 3.7; 0; 0; 0; 0
SECONDARY
Percentage of Participants With Post-treatment Relapse
3.0; 0; 0; 0; 0; 4.8

Summary

The purpose of this study is to evaluate the safety and efficacy of ABT-450/r/ABT-267 with or without ABT-333 and with or without ribavirin (RBV) in adult liver or renal transplant recipients with hepatitis C virus (HCV) genotype 1 or 4 (GT1 or GT4) infection.

Eligibility Criteria

Inclusion Criteria

  • Male or female, at least 18 years of age at the time of screening.
  • Currently taking an immunosuppressant regimen based on either tacrolimus or cyclosporine. Corticosteroids such as prednisone or prednisolone are permitted as components of the immunosuppressant regimen providing the dose is not more than 10 mg/day.
  • Hepatitis C virus (HCV) interferon (IFN) therapy treatment-naïve or -experienced, either pre- or post-liver or renal transplant.
  • Screening HCV genotype testing indicating infection with genotype 1 or 4 (GT1 or GT4) only.

Exclusion Criteria

  • Use of everolimus or sirolimus as part of the immunosuppressive regimen within 2 months of Screening Visit.
  • Use of any medications contraindicated for use with the study regimen as well as those that are contraindicated for use with either ritonavir or ribavirin within 2 weeks prior to study drugs administration or 10 half-lives (if known), whichever is longer.
  • Positive test result for Hepatitis B surface antigen (HBsAg) or anti-human immunodeficiency virus antibody (HIV Ab).
  • Documented history of post-transplant complications directly involving the hepatic or renal vasculature as appropriate to the organ transplanted, e.g., thrombosis of the portal vein, the hepatic artery and/or hepatic vein.
  • Clinically significant abnormalities, other than HCV infection, in a subject post-transplant based upon the medical history, physical examination, vital signs, laboratory profile and a 12-lead electrocardiogram (ECG) that make the subject an unsuitable candidate for this study in the opinion of the investigator.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01782495). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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