Sirolimus Conversions in African-American Renal Transplant Recipients



Status:Completed
Conditions:Renal Impairment / Chronic Kidney Disease
Therapuetic Areas:Nephrology / Urology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:August 2009
End Date:July 2014

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A Pilot Study Comparing Two Different Sirolimus-based Transition Regimens in African-American Renal Transplant Recipients

This study's focus is to compare the level effectiveness and safety of regimens involving
Sirolimus, Cellcept and steroid to Prograf, Sirolimus and steroid in African-American
recipients of kidney transplants.

A major concern in transplantation is finding a successful regimen of medications to lower
the potential for the body to reject the newly transplanted organ. The regimens in kidney
transplantation include tacrolimus, sirolimus, mycophenolate mofetil and steroids. This
study will compare the effectiveness and safety of a regimen including Sirolimus, Prograf,
and steroids compared to a regimen including Sirolimus, Cellcept and steroids. These
regimens have already been researched in the Caucasian population, and both drug regimens
are FDA approved. This study's focus is on the effectiveness and safety of these regimens in
African-Americans.

Inclusion Criteria:

- At least 18 years of age and able to give informed consent

- African-American ethnicity

- Received a first or second non-ECD cadaveric or living donor renal transplant

- Transplant occurred during the past 6 to 24 weeks

- Patient has stable graft function, defined as no change of greater than 30% of
baseline serum creatinine during the past month and no acute rejection in the past 6
weeks

- Estimated GFR using the modified MDRD equation of at least 40 mL/min10 at time of
enrollment into the study

- Currently receiving tacrolimus, mycophenolate mofetil (at least 1 gm per day), and
corticosteroids as their immunosuppression regimen.

Exclusion Criteria:

- Biopsy proven acute rejection episode that occurred within the past 6 weeks

- Malignancy within the past 3 years, except for non-melanoma skin cancer

- Any known intolerances to current immunosuppressant regimen necessitating withdrawal
of the offending agent

- Currently enrolled in an investigational trial

- Woman of child bearing potential not utilizing an effective form of birth control

- Patients with uncontrolled dyslipidemia, defined at serum fasting LDL >200 mg/dL or
serum fasting triglycerides >500 mg/dL.

- Patients with a spot urine protein to creatinine ratio of > 800 mg of protein per
gram of creatinine.

- WBC < 3,000 cells/mm3

- Platelets < 100,000 cells/mm3
We found this trial at
1
site
171 Ashley Avenue
Charleston, South Carolina 29425
843-792-1414
Medical University of South Carolina The Medical University of South Carolina (MUSC) has grown from...
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from
Charleston, SC
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