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Evaluation of Thymoglobulin Induction and Reduced Doses of Calcineurin Inhibitors on Liver Transplant Rejection

A Randomized, Controlled, Multi-Center Study of Thymoglobulin Induction Therapy With a Calcineurin Inhibitor Sparing Regimen in Liver Transplant Patients

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00117689
Enrollment
75
Registered
2005-07-08
Start date
2005-04-30
Completion date
2007-12-31
Last updated
2015-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Dysfunction, Rejection, Transplant, Transplantation, Liver

Keywords

Anti-T cell antibodies, Primary Liver Transplantation and Renal Dysfunction, Liver Transplant Rejection, Induction Therapy with reduction of Calcineurin inhibitors, Primary Liver Transplantation, Primary Transplant Rejection, Transplantation, Liver, Rejection, Transplant

Brief summary

This study involves the use of a drug called Thymoglobulin, which is approved in the US to treat kidney transplant rejection and in Canada to treat and prevent kidney transplant rejection. This study will evaluate the effect of Thymoglobulin induction therapy and reduced doses of calcineurin inhibitors on the incidence of liver rejection and will provide a basis for future evaluations of Thymoglobulin as an immunosuppressive agent to help decrease the incidence of liver transplant rejection. Subjects meeting all inclusion and exclusion criteria are eligible to participate in this study. Approximately 75 study subjects from up to 18 transplant centers in the United States and Canada will be enrolled in this 12-month study.

Interventions

BIOLOGICALThymoglobulin

Antibody inductions with tacrolimus and corticosteroid sparing maintenance therapy

DRUGCorticosteroid

For a minimum of 3 months

DRUGTacrolimus

Between Day 3 the last dose of Thymoglobulin

DRUGMycophenolate Mofetil

for at least 1 month posttransplant

Sponsors

Genzyme, a Sanofi Company
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Primary liver transplant recipient with Model for End-Stage Liver Disease (MELD) criteria documentation * Serum creatinine \> 1.5mg/dL at the time of transplant, or based on the value used to calculate the most recent pre-operative MELD Score for liver allocation * Ages greater than or equal to 18 years * If female, must not be lactating; must have a negative serum beta-human chorionic gonadotropin (HCG) test within 7 days prior to Study Day 0 (Day of Transplant); and must agree to practice an acceptable and reliable form of contraception during the study * Signed informed consent

Exclusion criteria

* Living donor or multiple organ transplants * Prior solid organ or bone marrow transplant recipient * Fulminant hepatic failure * Status 1 transplants * ABO incompatible transplants * Transplants utilizing livers from non heart-beating donors * Liver transplant candidates with \> 6 weeks of analysis * Donor with positive serology for hepatitis B surface antigen (HBsAg) * Evidence of human immunodeficiency virus (HIV) * Autoimmune hepatitis * History of chronic steroid or immunosuppressant use in the 90 days prior to transplant, except for inhaled corticosteroids to treat asthma * Recipient of investigational therapy within 90 days prior to transplant procedure * Known contraindication to administration of rabbit anti-thymocyte globulin * Acute viral illness * History of malignancy within 5 years, with the exception of adequately treated localized squamous or basal cell carcinoma of the skin without evidence of recurrence, and/or hepatocellular carcinoma * Illness other than primary liver disease (e.g. severe ischemic heart disease, left ventricular dysfunction, or pulmonary disease), which, in the opinion of the investigator, may significantly increase the risk of the transplantation procedure * Current drug and alcohol abuse that, in the opinion of the investigator, puts subjects at risk for poor compliance (no drug test required)

Design outcomes

Primary

MeasureTime frame
Freedom from biopsy-proven acute rejection (including humoral rejection)6 months

Secondary

MeasureTime frame
Explore the impact of Thymoglobulin on kidney function after transplant6 months
Explore the impact of Thymoglobulin on the prevention of liver transplant rejection, transplanted liver loss, death, and safety of Thymoglobulin after transplant.12 months

Countries

Canada, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026