Overview

This trial is active, not recruiting.

Condition kidney failure
Treatments cyclosporin + mycophenolate mofetil, everolimus + mycophenolate mofetil
Phase phase 3
Sponsor Centre Hospitalier Universitaire, Amiens
Collaborator Novartis
Start date May 2012
End date May 2017
Trial size 90 participants
Trial identifier NCT01595984, 2011-001385-18, PI10-PR-CHOUKROUN

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.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking open label
Primary purpose treatment
Arm
(Active Comparator)
cyclosporin + mycophenolate mofetil
antirejection drug, renal transplantation
(Experimental)
everolimus + mycophenolate mofetil
antirejection drug, renal transplantation

Primary Outcomes

Measure
Evolution of glomerular filtration rate measured by clearance of iohexol
time frame: one year

Eligibility Criteria

Male or female participants from 18 years up to 70 years old.

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.

Additional Information

Official title Randomized, Multicenter, Open-label, Comparative Study of Efficacy and Safety of Treatment With a Calcineurin Inhibitor (CNI), Associating Myfortic ® and Neoral ® Compared to a CNI-free Treatment, Combining Myfortic ® and Certican ® , in Adult Patients With de Novo Renal Transplant
Trial information was received from ClinicalTrials.gov and was last updated in June 2016.
Information provided to ClinicalTrials.gov by Centre Hospitalier Universitaire, Amiens.