drugset / Trial / NCT00518375

Study Comparing Graft Function in Renal Allograft Recepients Receiving Reduced or Standard Dose CsA With Sirolimus

NCT00518375

Phase 4 Completed 250 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedParallel-groupOpen-labelTreatment

Summary

This study evaluated renal graft function (based on calcuated creatinine clearance) 12 months after transplantation in patients receiving either a regimen of reduced dose or standard dose cyclosporine in combination with sirolimus and corticosteroids. The incidence of acute graft rejection at 6 and 12 months following transplantation and patient and graft survival at 12 months were evaluated also.

Timeline

Start
2000-04
Primary completion
Completion
2001-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclosporine Peptide
Background Sirolimus Small molecule

Indications

No indication recorded.