SAFETY, TOLERANCE, PHARMACOKINETIC STUDY OF ORAL MYCOPHENOLATE MOFETIL

$0M01FY2000RRNIH

University Of Minnesota Twin Cities, Minneapolis MN

Investigators

Linked publications & trials

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Abstract

This multi-center study aims to enroll 100 patients (10-15 at Fairview-University Medical Center) and is designed to test the safety, tolerance, efficacy, and concentration of drug in the blood after dosing of investigational mycophenolate Mofetil (MMF) oral suspension in pediatric kidney transplant patients. Children who are at least 3 months of age and weigh 5.4 or more kilograms and who have recieved a first or second transplant will be eligible for this study. Participants will recieve oral study medication twice daily for 36 months.

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