drugset / Trial / NCT00239005

Enteric-Coated Mycophenolate Sodium on Quality of Life in Patients With Gastrointestinal Symptoms Related to Mycophenolate Mofetil Therapy After Kidney Transplantation

NCT00239005

Phase 4 Completed 134 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

This open, multi-center randomized controlled study is designed to investigate the quality of life in patients with mycophenolate mofetil (MMF)-induced gastrointestinal (GI) adverse events after converting to enteric-coated mycophenolate sodium (EC-MPS).

Timeline

Start
2005-09
Primary completion
2008-03
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Mycophenolate Mofetil Small molecule 250 mg
Comparator Mycophenolate Mofetil Small molecule 500 mg
Subject Mycophenolate Sodium Unknown 180 mg Oral
Subject Mycophenolate Sodium Unknown 360 mg Oral

Indications

No indication recorded.