Assessment of Biomarkers for Recurrent HCV Infection Post-liver Transplantation

NCT ID: NCT00710801

Last Updated: 2011-09-15

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 40 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2005-05-31

Brief Summary

The purpose of this study is to learn about how different immunosuppressant therapies impact on recurrent hepatitis C virus infection in the new liver after liver transplant. We will be evaluating if Cyclosporin A has a superior effect against recurrent Hepatitis C virus (HCV) infection than Tacrolimus.

Detailed Description

We will address the hypothesis that CSA has a superior antiviral effect against HCV than Tacrolimus by assessing serial HCV RNA levels in serum. We plan to address the hypothesis that CSA is more efficient in limiting viremia than Tacrolimus and that viremia is predictive of long-term clinical outcome of hepatic fibrosis that is known to impact on both graft and patient survival

Conditions

Hepatitis C Virus

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• About to undergo a primary liver transplant (including living donor, split liver) and are HCV positive.
• Willing and capable of giving written consent for study participation
• Expected to be capable of study participation for full 24 months post-transplantation.
• Allograft biopsies will be possible
• Expected use of calcineurin inhibitor (Neoral or Tacrolimus) as primary immunosuppression An immunosuppressive regimen consisting of a calcineurin inhibitor (Neoral or Tacrolimus) in combination with Simulect and MYCOPHENOLATE SODIUM

Exclusion Criteria

• This is a multi-organ transplant or if the patient has previously been transplanted with any other organ.
• This is a liver transplant from a non-heart beating donor.
• This is an ABO incompatible transplant.
• Patients with serum creatinine level > 250 umol/L.
• The recipient is seropositive for human immunodeficiency virus (HIV) antibodies.
• Fulminant liver failure is the reason for transplant.
• Patient is participating in other clinical trial involving exploratory drug
• There is a known malignancy, or a history of malignancy, other than successfully treated non-metastatic basal or squamous cell carcinoma of the skin, or hepatocellular carcinoma less than 5 cm meeting Milan criteria for transplantation5.
• The patient is being transplanted for hepatic malignancy with greater than 5 known lesions.
• Severe coexisting disease is present or if any unstable medical condition is present which could affect the study objectives.
• A female transplant candidate is pregnant, lactating or of childbearing potential and not practicing an acceptable method of contraception.
• An unlicensed drug or therapy has been administered within one month prior to study entry or if such therapy is to be instituted post-transplantation.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Novartis

INDUSTRY

Sponsor Role: collaborator

University of Alberta

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Andrew L Mason, MD

Role: PRINCIPAL_INVESTIGATOR

University of Alberta

Locations

University of Alberta Hospital

Edmonton, Alberta, Canada

Countries

Canada

Other Identifiers

COLO400A2427

Identifier Type: -

Identifier Source: org_study_id