Clinical Trials Directory

Trials / Completed

CompletedNCT00238979

A Study to Investigate the Tolerability and Safety of Converting Stable Renal Transplant Recipients Who Receive Tacrolimus With or Without Corticosteroids From Mycophenolate Mofetil (MMF) to Enteric-coated Mycophenolate Sodium (EC-MPS)

A 6-month, 1-arm, Open-label Study to Investigate the Tolerability and Safety of Converting Stable Renal Transplant Recipients Who Receive Tacrolimus With or Without Corticosteroids From Mycophenolate Mofetil (MMF) to Enteric-coated Mycophenolate Sodium (EC-MPS)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
50 (planned)
Sponsor
Novartis Pharmaceuticals · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers

Summary

The aim of this study is whether a switch of stable renal transplant recipients who receive tacrolimus with or without corticosteroids from mycophenolate mofetil (MMF) to enteric-coated mycophenolate sodium (EC-MPS) is safe and well tolerated by the patients.

Conditions

Interventions

TypeNameDescription
DRUGEnteric-Coated Mycophenolate Sodium (EC-MPS)

Timeline

Start date
2003-01-01
Primary completion
2005-02-01
First posted
2005-10-14
Last updated
2011-11-02

Source: ClinicalTrials.gov record NCT00238979. Inclusion in this directory is not an endorsement.