Greater predictability in the oral dosing of cyclosporin A (CsA) and other P4503A4 substrates may minimize the number and duration of subtherapeutic or toxic events in organ transplantation, thus improving allograft survival. The goal of our research is to test the hypothesis that the oral bioavailability of CsA in stable renal transplant recipients under steady state conditions is largely determined by both enteric and hepatic P4503A4 catalytic activity.

Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
39
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
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