Tacrolimus/Everolimus Versus Tacrolimus/Enteric-Coated Mycophenolate Sodium

This study is currently recruiting participants. (see Contacts and Locations)
Verified May 2014 by University of Miami
Sponsor:
Information provided by (Responsible Party):
Gaetano Ciancio, University of Miami
ClinicalTrials.gov Identifier:
NCT01680861
First received: March 6, 2012
Last updated: May 19, 2014
Last verified: May 2014
  Purpose

A recent therapeutic strategy following renal transplantation includes simultaneous use of reduced calcineurin inhibitor (CNI) dosing and maximized use of a non-nephrotoxic, antiproliferative drug (inosine monophosphate dehydrogenase (IMPDH) or TOR inhibitor), with the goals of reducing/avoiding CNI nephrotoxicity, the incidence of acute rejection, and chronic allograft injury (CAI) (i.e., interstitial fibrosis/tubular atrophy), leading to more favorable longer-term patient and graft survival.1-7 Early corticosteroid withdrawal has also been used in the attempt to avoid well-known side effects while maintaining favorable patient and graft survival.8-10 While the investigators center and numerous other centers have also included single agent, antibody induction utilizing the lymphodepleting polyclonal antibody rabbit anti-human thymocyte globulin (ATG), nondepleting human anti-interleukin-2 receptor (CD25) monoclonal antibody daclizumab (Dac) or basiliximab, or lymphodepleting humanized anti-CD52 monoclonal antibody alemtuzumab,11-17 evidence now suggests that an even more effective induction strategy may include the combined use of more than one induction agent (each with fewer doses than if used alone), with the goal of bringing the kidney transplant recipient even closer (through more effectively timed lymphodepletion) to an optimally immunosuppressed state, allowing further reduction in long-term maintenance drug dosing.18-25 The investigators have now successfully used dual ATG/Dac induction therapy in both kidney-alone23-24 and simultaneous kidney-pancreas (SPK) transplantation,18-20 and a recent report from the investigators center of kidney-alone and SPK recipients shows that the addition of anti-CD25 to ATG for induction therapy more effectively delays the return of peripheral blood CD25+ cells.25 In the kidney-alone recipient study 3 doses of ATG were combined with 2 doses of Dac for induction,23-24 vs. the investigators previous studies utilizing single agent induction with 7 doses of ATG or 5 doses of Dac.4,16,17 Successful combination of ATG/basiliximab as dual induction in kidney transplantation has also been reported elsewhere,21-22 along with equivalency in clinical outcomes using daclizumab vs. basiliximab.13


Condition Intervention Phase
Transplant; Failure, Kidney
Drug: Tacrolimus, Everolimus
Drug: Tacrolimus, Myfortic
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Randomized, Open-Label Trial of Tacrolimus/Everolimus vs. Tacrolimus/Enteric-Coated Mycophenolate Sodium to Prevent Biopsy-Proven Acute Rejection and Chronic Allograft Injury in Adult, Primary Kidney Transplantation

Resource links provided by NLM:


Further study details as provided by University of Miami:

Primary Outcome Measures:
  • Induction therapy [ Time Frame: 1 year ] [ Designated as safety issue: Yes ]
    Induction therapy with ATG and basiliximab and corticosteroid withdrawal


Secondary Outcome Measures:
  • BPAR rate [ Time Frame: 1 year ] [ Designated as safety issue: Yes ]
    BPAR rate at 12 months as the single, primary study endpoint


Estimated Enrollment: 50
Study Start Date: November 2012
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: December 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Tacrolimus and Everolimus
Everolimus initiated within 24 hours post-transplant (i.e., immediately following randomization) at 0.75mg PO BID and will be adjusted in order to achieve target everolimus trough levels of 3-8 ng/ml.
Drug: Tacrolimus, Everolimus

Tacrolimus dosing (rTd) is planned, 0.1 mg/kg PO BID - beginning when serum Cr decreases to a level of <4 mg/dl (i.e., acceptable renal transplant function) postoperatively. Target tacrolimus trough levels during the first year post-transplant and thereafter will be 5-8 ng/ml.

Everolimus initiated at 0.75 PO BID and will be adjusted in order to achieve target everolimus trough levels of 3-8 ng/ml.

Corticosteroids will be given as per our center protocol, i.e., a bolus of 500 mg of methylprednisolone intravenously at surgery and daily x2, followed by 1.0 mg/kg, then 0.5 mg/kg orally until weaned off completely by 7 days postoperatively - the plan is for corticosteroids to be discontinued by 7 days postoperatively in both groups.

Other Name: Prograf, Zortress
Active Comparator: Tacrolimus and Myfortic
Randomized patients will receive reduced tacrolimus dosing (rTd) is planned, 0.1 mg/kg PO divided in two daily doses - beginning when serum Cr decreases to a level of <4 mg/dl (i.e., acceptable renal transplant function) postoperatively. Target tacrolimus trough levels during the first year post-transplant and thereafter will be 5-8 ng/ml.
Drug: Tacrolimus, Myfortic

Tacrolimus dosing (rTd) is planned, 0.1 mg/kg PO BID - beginning when serum Cr decreases to a level of <4 mg/dl (i.e., acceptable renal transplant function) postoperatively. Target tacrolimus trough levels during the first year post-transplant and thereafter will be 5-8 ng/ml.

EC-MPS 720 mg PO BID - beginning on 1st postoperative day.

Corticosteroids will be given as per our center protocol, i.e., a bolus of 500 mg of methylprednisolone intravenously at surgery and daily x2, followed by 1.0 mg/kg, then 0.5 mg/kg orally until weaned off completely by 7 days postoperatively - the plan is for corticosteroids to be discontinued by 7 days postoperatively in both groups.

Other Name: Prograf

Detailed Description:

A. Primary Objectives:

  1. The percentage of patients who develop chronic allograft injury (CAI) progression during the first 12 months post-transplant protocol biopsy (i.e., higher grade of IF/TA at either the 6 or 12 month protocol biopsy in comparison with the baseline biopsy).
  2. The incidence rate of biopsy-proven acute rejection (BPAR) during the first 12 months post-transplant.

B. Secondary Objectives:

  1. Adverse events including graft loss (death-censored and death-uncensored), and death at 12 months post-transplant.
  2. Incidence rate and severity (severity of CAI at 12 months as well), based upon careful review of all clinically indicated and protocol biopsies.
  3. Renal function as determined by serum creatinine and estimated glomerular filtration rate (eGFR) (calculated using the abbreviated MDRD formula) at 12, months post-transplant. Use of multivariable analysis to compare renal function as well as BPAR and CAI progression will also be performed (particularly, after adjusting for the significant effects of donor age, recipient age, race/ethnicity, and any other predictors).

5. Adverse events including withholding (for ≥ 28 days) or discontinuance of study medications (and reasons why), new onset diabetes mellitus after transplantation (NODAT), infections requiring hospitalization, and requirement of anti-lipid medication at 12 months post-transplant.

6. Avoidance of the requirement for maintenance corticosteroid therapy after renal transplantation.

7. Allowance of reduced maintenance tacrolimus dosing (rTd).

  Eligibility

Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Weight > 40 kg.
  • Deceased donor (SCD) or LD.
  • Donor-recipient 1 haplotype matched pairs with a minimum matching of 1 HLA DR antigen.
  • Negative standard cross match for T cells.
  • Pretransplant panel reactive antibodies of < 30%.

Exclusion Criteria:

  • Previously received or is receiving an organ transplant other than a kidney.
  • Donor organ with a cold ischemic time > 48 hours.
  • ABO incompatible donor kidney.
  • Recipients of T cell, or B cell crossmatch positive transplant.
  • Panel reactive antibody (PRA) >30%
  • HIV or Hepatitis C virus, or Hepatitis B virus antigenemia.
  • Current malignancy or a history of malignancy
  • Liver disease
  • Uncontrolled concomitant infections and/or severe diarrhea, vomiting, active upper gastro-intestinal tract malabsorption or an active peptic ulcer
  • Use of warfarin, fluvastatin, or herbal supplements during the study.
  • Use of astemizole, pimozide, cisapride, terfenadine, or ketoconazole.
  • Hypersensitivity to thymoglobulin, IL-2 receptor inhibitor monoclonal antibodies, tacrolimus, everolimus, MPA, or corticosteroids.
  • Pregnant or lactating.
  • Abnormal screening/baseline labs WBC, platelet count, triglycerides, and cholesterol Double kidneys,ECD, pediatric en-block, and donation after cardiac death (DCD)
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01680861

Contacts
Contact: Lois Hanson, R.N. 305-355-5314 lhanson2@med.miami.edu

Locations
United States, Florida
University of Miami Recruiting
Miami, Florida, United States, 33136
Contact: Lois Hanson, R.N.    305-355-5315    lhanson2@med.miami.edu   
Principal Investigator: Gaetano Ciancio, M.D. MBA         
Sponsors and Collaborators
Gaetano Ciancio
Investigators
Principal Investigator: Gaetano Ciancio, M.D. University of Miami
  More Information

No publications provided

Responsible Party: Gaetano Ciancio, Professor of Surgery, University of Miami
ClinicalTrials.gov Identifier: NCT01680861     History of Changes
Other Study ID Numbers: 20110126
Study First Received: March 6, 2012
Last Updated: May 19, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by University of Miami:
Kidney transplant patients

Additional relevant MeSH terms:
Renal Insufficiency
Kidney Diseases
Urologic Diseases
Mycophenolic Acid
Sirolimus
Mycophenolate mofetil
Everolimus
Tacrolimus
Antibiotics, Antineoplastic
Antineoplastic Agents
Therapeutic Uses
Pharmacologic Actions
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs
Antifungal Agents
Anti-Infective Agents
Anti-Bacterial Agents

ClinicalTrials.gov processed this record on July 22, 2014