A Prospective Study to Investigate Mycophenolic Acid (MPA) Exposure Through Area Under the Curve (AUC) in Renal Transplants Recipients Treated With Mycophenolate Mofetil (MMF) and After Conversion to Mycophenolate Sodium (EC-MPS)

PHASE4CompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

April 30, 2013

Primary Completion Date

March 31, 2015

Study Completion Date

March 31, 2015

Conditions
Renal Transplantation
Interventions
DRUG

Mycophenolate sodium

The conversion will be performed abruptly for all patients. Mycophenolate mofetil will be discontinued one day before the day of conversion (Day 1). Mycophenolate sodium will be introduced on day 1 with equivalent doses.

DRUG

Mycophenolate mofetil

Mycophenolate mofetil dose will be maintained or adjusted to keep 30 to 60 mg\*h ml-1.

Trial Locations (1)

90020090

Irmandade Da Santa Casa de Misericórdia de Porto Alegre, Porto Alegre

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Novartis

INDUSTRY

lead

Irmandade Santa Casa de Misericórdia de Porto Alegre

OTHER