drugset / Trial / NCT00634920

Evaluation of Early Conversion to Everolimus From Cyclosporine in de Novo Renal Transplant Recipients

NCT00634920

Phase 4 Completed 204 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is designed to evaluate if early conversion to everolimus from cyclosporine in de novo renal transplant recipients can improve long-term renal function and slow down the progression of chronic allograft nephropathy

Timeline

Start
2008-03
Primary completion
2013-05
Completion
2013-05

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cyclosporine Peptide
Subject Everolimus Small molecule 4 mg Oral
Background Basiliximab Monoclonal antibody 20 mg
Background Prednisone Other / unclassified
Background mycophenolic acid Small molecule 1080 mg
Background mycophenolic acid Small molecule 1440 mg