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 Corticosteroids Unknown — —
Background Enteric Coated Mycophenolate Sodium (EC-MPS) Unknown 1080 mg —
Background Enteric Coated Mycophenolate Sodium (EC-MPS) Unknown 1440 mg —