This is a 5 week crossover design bioequivalence study to compare the Abbott cyclosporine to Neoral cyclosporine. 50 patients will undergo an open-label, pharmacokinetic and safety, conversion study that consists of a screening period; Period I (two weeks of dosing with BID Neoral); Period II (two weeks of dosing with BID Abbott cyclosporine); and Period III (one week of dosing with BID Neoral). Pharmacokinetic parameters of cyclosporine will be determined during 12 hour pharmacokinetic profile testing, including Cmax, Tmax, Ctrough, AUC, Cavg and CL/F. Cyclosporine trough levels will be evaluated between 12-hour PK profile visit days. The safety and pharmacokinetics of Abbot cyclosporine will be compared to Neoral cyclosporine.

Project Start
1999-12-01
Project End
2001-02-28
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
40
Fiscal Year
2000
Total Cost
$206
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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