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The Comparison of Three Different Immunosuppressant Regimens in Kidney Transplant Recipients.

This study is ongoing, but not recruiting participants.

Sponsors and Collaborators: Mayo Clinic
Wyeth
Information provided by: Mayo Clinic
ClinicalTrials.gov Identifier: NCT00275522
  Purpose

The study is being done to compare the safety and effects (good and bad) of three different combinations of immunosuppression drugs used by kidney transplant recipients while also looking at their kidney function.


Condition Intervention Phase
Kidney Transplant
Drug: Sirolimus
Phase IV

MedlinePlus related topics:   Kidney Transplantation   

ChemIDplus related topics:   Tacrolimus    Mycophenolate Mofetil    Mycophenolate mofetil hydrochloride    Sirolimus    Tacrolimus anhydrous   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title:   A Randomized Open-Label Study to Compare the Safety and Efficacy of Two Different Sirolimus Regimens With a Tacrolimus + Mycophenolate Mofetil Regimen in De Novo Renal Allograft Recipients.

Further study details as provided by Mayo Clinic:

Primary Outcome Measures:
  • Calculated creatinine clearance at 12 months after transplantation.

Secondary Outcome Measures:
  • Calculated creatinine clearance at 26, 78, and 104 weeks post transplantation.
  • Serum creatinine at 26, 52, 78, and 104 weeks post transplantation.
  • Subject and graft survival at 26, 52, 78, and 104 weeks post transplantation.
  • Incidence and severity of biopsy-confirmed acute rejection at 26, 52, 78, and 108 weeks post transplantation.
  • Severity of rejection, including histological grade of the first acute rejection episode.

Estimated Enrollment:   16
Study Start Date:   December 2005

Detailed Description:

This is an open-label, randomized, comparative, multinational study. The study will be looking at the kidney function of kidney transplant recipients, while also comparing the safety and the effects (good and bad) of three different combinations of immunosuppression drugs in combination with prednisone, following treatment with Daclizumab (Zenapax). The three combinations are; (1) sirolimus and tacrolimus followed by the withdrawal of tacrolimus after three months; (2) sirolimus and mycophenolate mofetil (MMF); and (3) tacrolimus and MMF. The participants will be required to return to throughout the next 24 months following their transplant for physical exams, chest x-ray, blood, and urine tests. Participants will be put into one of three groups, and receive the study drugs starting on the day of transplant. Due to some drugs affecting the drug levels of sirolimus, participants need to agree not to take any new drugs during the study unless approved by the study doctor.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both

Criteria

Participants must be at least between the ages of 18 and 75, and will be receiving their first or second kidney transplant.

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00275522

Locations
United States, Minnesota
Mayo Clinic    
      Rochester, Minnesota, United States, 55905

Sponsors and Collaborators
Mayo Clinic
Wyeth

Investigators
Principal Investigator:     Mark D. Stegall, M.D.     Mayo Clinic    
  More Information


Study ID Numbers:   1302-04
First Received:   January 10, 2006
Last Updated:   December 20, 2007
ClinicalTrials.gov Identifier:   NCT00275522
Health Authority:   United States: Institutional Review Board

Study placed in the following topic categories:
Sirolimus
Clotrimazole
Miconazole
Tioconazole
Mycophenolate mofetil
Tacrolimus

Additional relevant MeSH terms:
Anti-Bacterial Agents
Anti-Infective Agents
Immunologic Factors
Antineoplastic Agents
Antifungal Agents
Therapeutic Uses
Physiological Effects of Drugs
Antibiotics, Antineoplastic
Immunosuppressive Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on October 10, 2008




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