drugset / Trial / NCT00646737

Conversion From Mycophenolate Mofetil to Mycophenolate Sodium in Renal Transplant

NCT00646737

Phase 4 Completed 18 enrolled Novartis
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and the tolerability of the substitution of mycophenolate mofetil for enteric-coated mycophenolate sodium in a population of stable renal transplant patients in Brazil, in a treatment regimen of immunosuppressants with tacrolimus and mycophenolate mofetil.

Timeline

Start
2008-05
Primary completion
2008-12
Completion
2008-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Mycophenolate Sodium Unknown

Indications

No indication recorded.