drugset / Trial / NCT00228020

Study of Safety and Efficacy of a Basiliximab, Mycophenolate Mofetil, Cyclosporine Microemulsion and Prednisone Combination Treatment Regimen in Pediatric Renal Allograft Recipients

NCT00228020 ↗

Phase 3 Completed 212 enrolled Novartis
RandomizedParallel-groupDouble-blindPrevention

Summary

The aim of this study is assess the safety and efficacy of the treatment regimen of basiliximab ,cyclosporine microemulsion, MMF, and prednisone combined compared to cyclosporine microemulsion, MMF and prednisone in the time to first biopsy proven acute rejection episode or treatment failure during the first 6 months post-transplantation in pediatric renal allograft recipients.

Timeline

Start
2001-05
Primary completion
2006-01
Completion
—

Outcome

Missed primary endpoint

paper hazard ratio 0.72, two-sided 90% confidence interval 0.416-1.26, n.s. PMID 19005406 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Basiliximab Monoclonal antibody — —
Background Cyclosporine Peptide — —
Background Mycophenolate Mofetil Small molecule — —
Background Prednisone Other / unclassified — —

Indications

No indication recorded.