Phase IV Study to Evaluate Calcineurin Inhibitor Reduced, Steroid Free Immunosuppression After Renal Transplantation

In this triple arm, prospectively randomized multi centre phase IV study 200 patients per study arm will be investigated for 12 months.

Based on the results of the Symphony study the low dose tacrolimus study arm will be modified to further improve efficacy (prevention of BPAR, best possible renal function) and safety (adverse event profile regarding infections, cardiovascular risk factors, malignant tumours) of immunosuppression. For this, CNI will be reduced and in addition the rate of steroid free patients after 1 week will be maximized to achieve a long lasting improved post surgical cardiovascular risk profile (in particular concerning de novo induction of diabetes mellitus and other adverse events caused by steroids). Safety should be increased without loss of efficacy of immunosuppression (measured in rejection rate and allograft loss rate) as compared to an immune suppressive therapy comprising steroids. Therefore, following the successful study arm of the Symphony study, immunosuppression in the first of the three study arms comprises a steroid in combination with Advagraf and CellCept in addition to a two dose induction therapy with Simulect (group A). The regimen of the second study arm is similar but discontinues steroids on day seven after transplantation (group B). Therapy of group three is similar to group B but Simulect is replaced by T-cell depleting polyclonal antibodies (Thymoglobulin) (group C).

Inclusion criteria

• Post mortal kidney donation or living donation
• Primary and secondary renal transplantation, unless the graft was lost due to severe rejection within the first year
• PRA level ≤ 20%.
• Recipient ≥ 18 to 75 years of age
• AB0-compatible
• Negative crosshatch
• Patients with a signed informed consent form
• Women of child-bearing age must agree to an efficient contraception

Exclusion criteria

• Third or multiple transplantation
• Transplantation per a "non-heart beating" donor
• HLA-identical living donation
• Incompatibility to study medication (allergy, intolerance, hypersensitivity)
• Patients with existing malignant underlying disease or tumour anamnesis < 5 years. Exception: basaloma or squamous cell carcinoma of the skin after successful therapy
• Female patients who do not use a safe method of contraception
• Patients with clinically significant, uncontrolled infectious diseases (incl. HIV) and/or severe diarrhoea, emesis, active malabsorption of the upper gastrointestinal tract or active peptic ulcer
• Patients currently, resp. within the last 30 days, participating in other studies
• Primary focal-sclerosing glomerulonephritis and membranoproliferative glomerulonephritis as an underlying disease
• Autoimmune disease as underlying disease (collagen diseases, colitis, HUS, SLE) which might require chronic cortisone therapy
• Additional disease requiring temporary or chronic cortisone therapy (including inhalation medicine)
• Chronic hepatitis B and hepatitis C infection
• Thrombopenia < 70.000/mm3 or leukopenia < 2.500/mm3 or neutropenia < 1500/ mm3.
• Patients with hepatocirrhosis Child B or C or another severe disease of the liver
• Patients with symptoms of a significant somatic or psychiatric / mental illness. Patients who are not able to realize nature, relevance and consequences of the clinical trial and who are not able to comply, to cooperate and communicate adequately and to follow the instructions of the study or even to give their informed consent (according to § 40 article 4 and § 41 article 2 and 3 AMG).
• Patients who possibly depend on the sponsor or the trial physician
• Patients with signs of drug abuse or alcohol abuse
• Patients taking additional medicines with known interactions with the immune suppressive substances (MMF and tacrolimus) that preclude an adequate control of the immunosuppression
• Cold ischemia time of donor kidney > 30 hours
• Pregnant or nursing patients