drugset / Trial / NCT01023542

CNI-free "Bottom"-up Immunosuppression in Patients Undergoing Liver Transplantation

NCT01023542

RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of the trial is to evaluate efficacy and safety of delayed introduction (up to 30 days post-transplantation in patients without signs of acute rejection that had received an aIL-2 induction and MMF) of either cyclosporine or everolimus versus a 5-day delay of cyclosporine in combination with MMF.

Timeline

Start
2011-06
Primary completion
2014-07
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cyclosporine Peptide
Subject Everolimus Small molecule