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Comparative pharmacokinetics of tacrolimus in stable pediatric allograft recipients converted from immediate‐release tacrolimus to prolonged‐release tacrolimus formulation
Author(s) -
Rubik Jacek,
Debray Dominique,
Iserin Franck,
Vondrak Karel,
SellierLeclerc AnneLaure,
Kelly Deirdre,
Czubkowski Piotr,
Webb Nicholas J. A.,
Riva Silvia,
D'Antiga Lorenzo,
Marks Stephen D.,
Rivet Christine,
Tönshoff Burkhard,
Kazeem Gbenga,
Undre Nasrullah
Publication year - 2019
Publication title -
pediatric transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 69
eISSN - 1399-3046
pISSN - 1397-3142
DOI - 10.1111/petr.13391
Subject(s) - tacrolimus , medicine , cmax , pharmacokinetics , confidence interval , urology , regimen , liver transplantation , kidney , gastroenterology , pharmacology , transplantation
This study was a Phase II , open‐label, multicenter, single‐arm, cross‐over study comparing the pharmacokinetics ( PK ) of tacrolimus in stable pediatric kidney, liver, or heart allograft recipients converted from immediate‐release tacrolimus ( IR ‐T) to prolonged‐release tacrolimus ( PR ‐T). In Days −30 to −1 of screening period, patients received their IR ‐T‐based regimen; during Days 1‐7, patients received study IR ‐T (same dose as screening). On Day 7, the first 24‐hours PK profile was taken; patients were then converted to PR ‐T (1 mg:1 mg), with a second 24‐hours PK profile taken on Day 14. The primary end‐point was tacrolimus area under the blood concentration–time curve over 24 hours ( AUC 24 ); secondary end‐points were maximum concentration C max and concentration at 24 hours C 24 . The predefined similarity interval for confidence intervals ( CI s) of least squares mean ( LSM ) ratios was 80%‐125%. The PK analysis set comprised 74 pediatric transplant recipients (kidney, n = 45; liver, n = 28; heart, n = 1). PR ‐T: IR ‐T LSM ratio (90% CI ) was similar overall for AUC 24 , max , and C 24 , and for kidney and liver recipients for AUC 24 ( LSM ratio, kidney 91.8%; liver 104.1%) and C 24 (kidney 90.5%; liver 89.9%). Linear relationship was similar between AUC 24 and C 24 , and between PR ‐T and IR ‐T (rho 0.89 and 0.84, respectively), suggesting that stable pediatric transplant recipients can be converted from IR ‐T to PR ‐T at the same total daily dose, using the same therapeutic drug monitoring method.