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.