Comparison of Efficacy and Safety of Treatment With a Calcineurin Inhibitor (CNI)Versus a CNI-free Treatment in Renal Transplantation (CIME)
Phase 3
- Conditions
- Kidney Failure
- Interventions
- Registration Number
- NCT01595984
- Lead Sponsor
- Centre Hospitalier Universitaire, Amiens
- Brief Summary
The main objective of this protocol is to compare the impact on renal function of two different immunosuppressive regimens in patients with de novo renal transplant.
Renal function will be accurately evaluated by measuring the clearance of iohexol.
The protocol will also evaluate the efficacy and safety in a short term of these two different immunosuppressive regimens.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
- Males and Females aged between 18 and 70.
- Patient receiving a first or second kidney transplant from a deceased donor, living related or unrelated.
- Patient with a maximum PRA <20%.
- Patient wishing and being able to participate fully to the study, and having given a written consent.
- Patient covered by a social insurance or beneficiary of such a regime.
- Women of childbearing age must use a recognized method of contraception throughout the study period and continue for 8 weeks after discontinuation of study treatment.
Exclusion Criteria
- Patient receiving a kidney from a heart attack donor , or an ABO incompatible donor or a donor with a positive T-cross match.
- Patient with a maximum PRA> 20% twice.
- Cold ischemic time > 36 hours.
- Patients with thrombocytopenia (<75000/mm3), neutropenia (<1 500 / mm3), leukopenia (<2 500 / mm3) or a hemoglobin concentration <8 g / dl, at inclusion visit.
- Patient with severe hyperlipidemia: total cholesterol ≥ 9 mmol / l (≥ 3.50 g / l) and / or triglycerides ≥ 8.5 mmol/l (≥ 7.5 g / l) despite appropriate lipid-lowering therapy.
- Patient with known HIV positive status, know active hepatitis B or C. Recipients of an organ from a donor with positive HIV status, hepatitis B or hepatitis C are excluded.
- Patient with severe systemic infections requiring continued therapy.
- Treatment with an experimental drug within 4 weeks before the first dose of study treatment.
- Patient for whom the initial disease or other pathology requires a long-term corticosteroid treatment.
- Patient with a history of hypersensitivity or known contra-indications for macrolide or inhibitors of mTORs drugs; drugs similar to Myfortic ® (ERL080) or other components of the formulation such as lactose, or cyclosporine, or prednisone (Cortancyl ®), or Thymoglobuline ® or Iohexol.
- Patient with a malignant disease or a history of malignancy over the past 5 years except squamous-cell or basal cell carcinoma wich was excised.
- Medical condition or surgical procedure, except transplantation, which could exclude the patient in the opinion of the investigator.
- Patient with symptoms of mental or significant somatic illness. Disability to cooperate or communicate with the investigator.
- Pregnant, sucking or of childbearing age and refusing or being unable to use a recognized contraceptive method.
- Patient under guardianship, or any patient protected by law.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Cyclosporin + Mycophenolate mofetil cyclosporin + mycophenolate mofetil - Everolimus + mycophenolate mofetil everolimus + mycophenolate mofetil -
- Primary Outcome Measures
Name Time Method Evolution of glomerular filtration rate measured by clearance of iohexol one year
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
Nephrology department, Hospital University of Amiens
🇫🇷Amiens, France
Nephrology Department, University Hospital of Montpellier
🇫🇷Montpellier, France