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- Title
Sitagliptin, an dipeptidyl peptidase-4 inhibitor, does not alter the pharmacokinetics of the sulphonylurea, glyburide, in healthy subjects.
- Authors
Mistry, Goutam C.; Bergman, Arthur J.; Zheng, Wei; Hreniuk, David; Zinny, Miguel A.; Gottesdiener, Keith M.; Wagner, John A.; Herman, Gary A.; Ruddy, Marcella
- Abstract
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • No data are available on the potential drug interaction of sitagliptin and glyburide. • Sitagliptin belongs to a new class of drugs called DPP-4 inhibitors recently approved for the treatment of Type 2 diabetes. WHAT THIS STUDY ADDS • Glyburide is a commonly used sulphonylurea medication to treat Type 2 diabetes. • Combination therapy is often required to achieve adequate glucose control in Type 2 diabetes. • Sitagliptin does not appear to interfere with glyburide pharmacokinetics and therefore may be potentially co-administered with glyburide for the treatment of Type 2 diabetes. AIMS Sitagliptin, a dipeptidyl peptidase-4 inhibitor, is an incretin enhancer that is approved for the treatment of Type 2 diabetes. Sitagliptin is mainly renally eliminated and not an inhibitor of CYP450 enzymes in vitro. Glyburide, a sulphonylurea, is an insulin sensitizer and mainly metabolized by CYP2C9. Since both agents may potentially be co-administered, the purpose of this study was to examine the effects of sitagliptin on glyburide pharmacokinetics. METHODS In this open-label, randomized, two-period crossover study, eight healthy normoglycaemic subjects, 22–44 years old, received single 1.25-mg doses of glyburide alone in one period and co-administered with sitagliptin on day 5 following a multiple-dose regimen for sitagliptin (200-mg q.d. ×6 days) in the other period. RESULTS The geometric mean ratios and 90% confidence intervals [(glyburide + sitagliptin)/glyburide] for AUC0–∞ and Cmax were 1.09 (0.96, 1.24) and 1.01 (0.84, 1.23), respectively. CONCLUSION Sitagliptin does not alter the pharmacokinetics of glyburide in healthy subjects.
- Subjects
TYPE 2 diabetes; DRUG interactions; PHARMACOKINETICS; PEPTIDASE; CHEMICAL inhibitors
- Publication
British Journal of Clinical Pharmacology, 2008, Vol 66, Issue 1, p36
- ISSN
0306-5251
- Publication type
Article
- DOI
10.1111/j.1365-2125.2008.03148.x