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Efficacy of Sirolimus-Based, Steroid Avoidance Immunosuppression African Americans

Primary Purpose

End Stage Renal Disease, Kidney Transplantation

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Sirolimus
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End Stage Renal Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: African American recipient race Solitary cadaveric or living donor renal transplantation Age ≥18years at the time of transplantation Negative pregnancy serum test in females with childbearing potential Exclusion Criteria: Age < 18 years at the time of transplantation Multi-organ transplant recipient Currently taking steroids White Blood Cell Count < 3,000 Platelet count < 100,000 Triglycerides >400mg/dL Cholesterol > 350 mg/dL Unwillingness to comply with study procedures Allergic reaction to sirolimus Allergy to polyclonal antilymphocyte drugs (Thymoglobulin)

Sites / Locations

  • University of Michigan Health Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Sirolimus, steroid avoidance arm

Arm Description

Thymoglobulin induction, sirolimus and no maintenance corticosteroid.

Outcomes

Primary Outcome Measures

Cumulative One-year Acute Rejection Rates
To test the efficacy of Sirolimus (SRL)-based steroid avoidance regimen in high risk de novo renal allograft recipients. Efficacy endpoints for this objective is: cumulative one-year acute rejection rates of the transplant
One-year Graft Survival
To test the efficacy of SRL-based steroid avoidance regimen in high risk de novo renal allograft recipients. Efficacy endpoints for this objective is: one-year graft survival
One-year Patient Survival
To test the efficacy of SRL-based steroid avoidance regimen in high risk de novo renal allograft recipients. Efficacy endpoints for this objective is: one-year patient survival

Secondary Outcome Measures

Incidence of Post Transplant Diabetes
To determine whether SRL-based steroid avoidance maintenance regimen is associated with decreased rates of metabolic complications. Endpoint is incidence of posttransplant diabetes mellitus
Drug-treated Dyslipidemic Syndrome
To determine whether SRL-based steroid avoidance maintenance regimen is associated with decreased rates of metabolic complications. Endpoint is drug-treated dyslipidemic syndrome
Blood Pressure Control
To determine whether SRL-based steroid avoidance maintenance regimen is associated with decreased rates of metabolic complications. Endpoint is number of people who had their blood pressure in the target control range with or without medication

Full Information

First Posted
September 13, 2005
Last Updated
February 27, 2018
Sponsor
University of Michigan
Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer
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1. Study Identification

Unique Protocol Identification Number
NCT00189202
Brief Title
Efficacy of Sirolimus-Based, Steroid Avoidance Immunosuppression African Americans
Official Title
Efficacy of Sirolimus-Based, Steroid Avoidance Maintenance Immunosuppression in Black de Novo Kidney Transplant Recipients
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
August 2004 (undefined)
Primary Completion Date
July 1, 2008 (Actual)
Study Completion Date
July 1, 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer

4. Oversight

5. Study Description

Brief Summary
African Americans receiving a kidney transplant are considered at high risk for early rejection of their transplanted kidney and require more immunosuppression to maintain their kidney transplant function. This increase in immunosuppression puts this group at risk for drug-related toxicities and complications such as post-transplant diabetes. This study will evaluate: Whether a sirolimus based steroid avoidance regimen in African Americans may decrease the risks of drug-related toxicities, Decreased rates of metabolic complications such as post-transplant diabetes, The effect of Sirolimus plus a reduced dose cyclosporine on renal allograft function.
Detailed Description
This is an open labeled prospective trial with race matched historical controls. The treatment group (experimental arm) will be African American de novo solitary renal transplant recipients. The control arm will consist of race matched solitary renal transplant recipients who received a Cyclosporine (CsA) -based immunosuppressive regimen. The subjects will be matched for organ source (living donor vs. cadaveric). The experimental treatment arm will have an immunosuppression regimen consisting of Sirolimus, Reduced dose cyclosporine, Thymoglobulin, and only 3 doses of steroids.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Renal Disease, Kidney Transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
49 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sirolimus, steroid avoidance arm
Arm Type
Experimental
Arm Description
Thymoglobulin induction, sirolimus and no maintenance corticosteroid.
Intervention Type
Drug
Intervention Name(s)
Sirolimus
Other Intervention Name(s)
Rapamune
Intervention Description
Thymoglobulin induction, sirolimus and no maintenance corticosteroid
Primary Outcome Measure Information:
Title
Cumulative One-year Acute Rejection Rates
Description
To test the efficacy of Sirolimus (SRL)-based steroid avoidance regimen in high risk de novo renal allograft recipients. Efficacy endpoints for this objective is: cumulative one-year acute rejection rates of the transplant
Time Frame
12 months
Title
One-year Graft Survival
Description
To test the efficacy of SRL-based steroid avoidance regimen in high risk de novo renal allograft recipients. Efficacy endpoints for this objective is: one-year graft survival
Time Frame
12 months
Title
One-year Patient Survival
Description
To test the efficacy of SRL-based steroid avoidance regimen in high risk de novo renal allograft recipients. Efficacy endpoints for this objective is: one-year patient survival
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Incidence of Post Transplant Diabetes
Description
To determine whether SRL-based steroid avoidance maintenance regimen is associated with decreased rates of metabolic complications. Endpoint is incidence of posttransplant diabetes mellitus
Time Frame
12 months
Title
Drug-treated Dyslipidemic Syndrome
Description
To determine whether SRL-based steroid avoidance maintenance regimen is associated with decreased rates of metabolic complications. Endpoint is drug-treated dyslipidemic syndrome
Time Frame
12 months
Title
Blood Pressure Control
Description
To determine whether SRL-based steroid avoidance maintenance regimen is associated with decreased rates of metabolic complications. Endpoint is number of people who had their blood pressure in the target control range with or without medication
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: African American recipient race Solitary cadaveric or living donor renal transplantation Age ≥18years at the time of transplantation Negative pregnancy serum test in females with childbearing potential Exclusion Criteria: Age < 18 years at the time of transplantation Multi-organ transplant recipient Currently taking steroids White Blood Cell Count < 3,000 Platelet count < 100,000 Triglycerides >400mg/dL Cholesterol > 350 mg/dL Unwillingness to comply with study procedures Allergic reaction to sirolimus Allergy to polyclonal antilymphocyte drugs (Thymoglobulin)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Akinlolu Ojo, MD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan Health Center
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

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Efficacy of Sirolimus-Based, Steroid Avoidance Immunosuppression African Americans

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