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Reduction or Discontinuation of CNI's With Conversion to Everolimus-Based Immunosuppresion
This study is currently recruiting participants.
Verified by Rabin Medical Center, September 2005
Sponsors and Collaborators: Rabin Medical Center
Novartis
Information provided by: Rabin Medical Center
ClinicalTrials.gov Identifier: NCT00443508
  Purpose

This study is design to compare two different strategies aiming to lessen the degree of the ongoing process of allograft injury either by removing tacrolimus from the maintenance immunosuppressive protocol or by reducing tacrolimus dose.

The primary goal is to assess the change in renal function at 6 and 12 months after conversion using creatinine levels and calculated creatinine clearance.

The study will include two groups: The study group of 30 patients and a matched control group with creatinine levels at similar range.


Condition Intervention Phase
Kidney Diseases
Drug: adding Certican to therapy
Drug: reducing Tacrolimus
Phase IV

MedlinePlus related topics: Kidney Transplantation
Drug Information available for: Tacrolimus Everolimus Tacrolimus anhydrous
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Reduction or Discontinuation of Calcineurine Inhibitors With Conversion to Everolimus-Based Immunosuppresion to Alleviate Chronic Allograft Nephropathy (CAN) in Kidney Transplant Recipients: A Prospective Randomized Study

Further study details as provided by Rabin Medical Center:

Primary Outcome Measures:
  • The primary goal is to assess the change in renal function
  • at 6 and 12 months after conversion using creatinine levels
  • and calculated creatinine clearance.

Secondary Outcome Measures:
  • The secondary aim is to assess changes in cardiovascular risks at
  • 12 months after conversion (glucose control., cholesterol and
  • triglyceride levels and hypertension control), incidence of
  • acute and chronic rejection and graft and patient survival rates.

Estimated Enrollment: 60
Study Start Date: February 2007
Estimated Study Completion Date: February 2010
Detailed Description:

This study is design to compare two different strategies aiming to lessen the degree of the ongoing process of allograft injury either by removing tacrolimus from the maintenance immunosuppressive protocol or by reducing tacrolimus dose.

The primary goal is to assess the change in renal function at 6 and 12 months after conversion using creatinine levels and calculated creatinine clearance.

The study will include two groups: The study group of 30 patients and a matched control group with creatinine levels at similar range.

Patients will undergo the following baseline studies:

  1. Doppler ultrasound to exclude any mechanical or a vascular problem.
  2. A kidney biopsy to define the histological changes (degree of interstitial fibrosis, tubular and glomerular changes). The biopsies will be stained also for C4D and for fibrinogenic markers (TGF-beta, and collagen).
  3. A 24-hour urine protein excretion and creatinine clearance
  4. Echocardiography study
  5. Carotid Ultrasound

The following parameters will be monitored every clinic visit throughout the study period:

  1. SMA-12 including creatinine levels.
  2. A complete blood count.
  3. Cholesterol, HDL-cholesterol and triglyceride levels.
  4. Blood pressure measurements (X2)
  5. The number of blood pressure medications.
  6. Cholesterol lowering medication requirement
  7. Urine protein excretion (quantitative spot-test )
  8. Protein amount in the urine

Study end points:

The data will be evaluated based on an intention to treat analysis and the following parameters will be compared between the two groups:

  1. Creatinine levels and calculated creatinine clearance
  2. Spot urine for Cr./protein ratio
  3. 24-hr. protein excretion
  4. Change in peak diastolic and mean arterial blood pressure
  5. The number and dosage of blood pressure medications
  6. Cholesterol, HDL and triglyceride levels
  7. Proportion of patients on cholesterol lowering agents
  8. Number and severity of biopsy proven acute rejection episodes
  9. Incidence of biopsy proven chronic rejection. (depends on per protocol biopsy at end of study)
  10. Patient and graft survival
  Eligibility

Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients on CNI FK < 5 ng/m"l with MPA / Imuran with or without steroids
  • Renal impairment GFR between 30 - 70 m"l/minute/
  • Patient who signed Informed consent
  • Patient with no contraindication to renal biopsy
  • Women who are not pregnant and will use contraception

Exclusion Criteria:

  • Proteinuria > 100 m"g/mmol Creatinine
  • Acute rejection during 3 months before screening
  • WBC < 2500, plt < 50,000,
  • Nephropathy due to polyoma virus
  • Patients on other investigational drugs
  • Patients on rapamycin
  • Patients with HIV or other systemic infection
  • Inability to comply with protocol requirements
  • Active or history of malignancy
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00443508

Contacts
Contact: Eytan Mor, Prof 00973 3 9376528 emor@clalit.org.il
Contact: Ruti rahamimov, Dr 00973 3 9376528 rutir@clalit.org.il

Locations
Israel
Transplantation department, rabin Medical Center Recruiting
Petach Tikva, Israel, 49202
Contact: Eytan Mor, Prof     00937 3 9376528     tikim@clalit.org.il    
Principal Investigator: Eytan Mor, Prof            
Sub-Investigator: Ruti Rahamimov, Dr            
Sub-Investigator: Alex Yusim, Dr            
Sponsors and Collaborators
Rabin Medical Center
Novartis
Investigators
Principal Investigator: Eytan Mor, Prof Rabin Medical Center, head of Transplantation department
  More Information

Study ID Numbers: CRAD001AIL01
Study First Received: March 4, 2007
Last Updated: March 5, 2007
ClinicalTrials.gov Identifier: NCT00443508  
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Rabin Medical Center:
everolimus
renal transplant
tacrolimus
Certican
CHRONIC ALLOGRAFT NEPHROPATHY
Renal transplant patients

Study placed in the following topic categories:
Everolimus
Urologic Diseases
Tacrolimus
Kidney Diseases

Additional relevant MeSH terms:
Immunologic Factors
Physiological Effects of Drugs
Immunosuppressive Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009