Premium
Dose‐proportionality of a final market image sitagliptin formulation, an oral dipeptidyl peptidase‐4 inhibitor, in healthy volunteers
Author(s) -
Bergman Arthur,
Mistry Goutam C.,
Luo WenLin,
Liu Q.,
Stone Julie,
Wang Amy,
Zeng Wei,
Chen Li,
Dilzer Stacy,
Lasseter Kenneth,
Herman Gary A.,
Wagner John A.,
Krishna Rajesh
Publication year - 2007
Publication title -
biopharmaceutics and drug disposition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.419
H-Index - 58
eISSN - 1099-081X
pISSN - 0142-2782
DOI - 10.1002/bdd.559
Subject(s) - sitagliptin , dipeptidyl peptidase 4 inhibitor , sitagliptin phosphate , pharmacokinetics , dipeptidyl peptidase 4 , medicine , urine , dipeptidyl peptidase , pharmacology , oral administration , urology , endocrinology , diabetes mellitus , type 2 diabetes , chemistry , enzyme , biochemistry
Sitagliptin is a highly selective orally active dipeptidyl peptidase‐4 inhibitor recently approved in the United States for the treatment of type 2 diabetes. Ten healthy subjects received single oral doses of 25, 50, 100, 200 and 400 mg final market image tablets in five separate treatment periods in randomized fashion to assess dose proportionality. Blood (up to 72 h post‐dose) and urine (up to 24 h post‐dose) samples for sitagliptin pharmacokinetic analysis were collected at pre‐specified times following administration of sitagliptin. Dose‐proportionality of AUC 0– ∞ , C max and C 24 h was assessed using a power‐law model. The results of this study indicate that plasma AUC 0− ∞ increased in a dose‐proportional manner over the 25–400 mg dose range. Over the same dose range, plasma C max increased in a greater than dose‐proportional manner and C 24 h increased in a modestly less than dose proportional manner. No clinically meaningful differences in T max or apparent t 1/2 were noted across the dose range. Differences in the percentage of the sitagliptin dose excreted unchanged in urine (72.5% pooled across doses) and renal clearance (344 ml/min pooled across doses) were not statistically significant. Sitagliptin was generally well tolerated at all the doses evaluated. Copyright © 2007 John Wiley & Sons, Ltd.