Renal Failure Clinical Trial
Official title:
Prospective, Rand, Open-label, Single-center, 2 Sequence, 3 Period Crossover Study to Compare the Steady State PK of Once-Daily-Extended Release LCP-Tacro to Generic Tacrolimus Capsules Twice Daily in Stable A A Renal Transplant pt.
Open label, prospective, single-center, randomized, two sequence, three period crossover study to compare the steady state pharmacokinetics of LCP-Tacro tables to generic tacrolimus capsules administered twice daily in stable African-American renal transplant patients.
This is open label, prospective, single-center, randomized, two sequence, three period
crossover study to compare the steady state pharmacokinetics of once daily dosing of
LCP-Tacro tablets to tacrolimus capsules administered twice daily in stable African American
kidney transplant patients.
Approximately 72 male and female African American renal transplant patients on table
immunosuppression regimens will be randomly assigned in a 1:1 ratio to one of two sequences:
Sequence 1: (n=36) 18 patients requiring less than 0.15 mg/kg/day and 18 patients requiring
equal to or greater than 0.15 mg/kg/day. Patients will continue on generic tacrolimus
capsules on days 1-7 (24 hours PK profile on day 7) then patients are switched to LCP-Tacro
tablets (at 15% lower dose of twice daily generic tacrolimus) on day 8.
Sequence 2: (n=36) 18 patients requiring less than 0.15 mg/kg/day and 18 patients requiring
equal to or greater than 0.15 mg/kg/day. Patients will receive LCP-Tacro tablets (at 15%
lower dose than generic tacrolimus twice daily formulation) on days 1-7 (24 hour PK profile
on day 7) patients are switched back to twice daily generic tacrolimus treatment beginning on
day 8.
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