Pharmacokinetics of Empagliflozin, a Sodium Glucose Cotransporter-2 (SGLT-2) Inhibitor, Coadministered with Sitagliptin in Healthy Volunteers

被引:50
作者
Brand, Tobias [1 ]
Macha, Sreeraj [2 ]
Mattheus, Michaela [3 ]
Pinnetti, Sabine [1 ]
Woerle, Hans J. [3 ]
机构
[1] Boehringer Ingelheim Pharma GmbH & Co KG, Dept Translat Med, D-88397 Biberach, Germany
[2] Boehringer Ingelheim Pharmaceut Inc, Ridgefield, CT 06877 USA
[3] Boehringer Ingelheim Pharma GmbH & Co KG, D-55216 Ingelheim, Germany
关键词
BI; 10773; Diabetes; Dipeptidyl peptidase-4 inhibitor; Drug-drug interaction; Empagliflozin; Sitagliptin; Sodium glucose cotransporter-2 inhibitor; TYPE-2; DIABETES-MELLITUS; DIPEPTIDYL-PEPTIDASE-IV; DOUBLE-BLIND; BI; 10773; PHARMACODYNAMICS; TOLERABILITY; HOMEOSTASIS; SAFETY;
D O I
10.1007/s12325-012-0055-3
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This randomized, open-label, crossover study investigated potential drug-drug interactions between the sodium glucose cotransporter-2 (SGLT-2) inhibitor empagliflozin and the dipeptidyl peptidase-4 (DPP-4) inhibitor sitagliptin. Empagliflozin is a potent and selective SGLT-2 inhibitor that lowers blood glucose levels by inhibiting renal glucose reabsorption, leading to an increase in urinary glucose excretion. Sitagliptin lowers blood glucose through an insulin-dependent mechanism of action. Sixteen healthy male volunteers received three treatments (A, B, C) in one of two treatment sequences (AB then C, or C then AB). In treatment AB, 50 mg empagliflozin was administered once daily (q.d.) for 5 days (treatment A), immediately followed by coadministration of 50 mg empagliflozin q.d. and 100 mg sitagliptin q.d. over 5 days (treatment B). In treatment C, 100 mg sitagliptin was administered q.d. for 5 days. A washout period of a parts per thousand yen7 days separated treatments AB and C. Coadministration of sitagliptin with empagliflozin did not have a clinically relevant effect on the area under the concentration-time curve of the analyte in plasma at steady state over a uniform dosing interval tau (AUC(tau,ss)) (geometric mean ratio [GMR] 110.4; 90% confidence interval [CI] 103.9, 117.3) or maximum measured concentration of the analyte in plasma at steady state over a uniform dosing interval tau (C (max,ss)) (GMR 107.6; 90% CI 97.0, 119.4) of empagliflozin. Coadministration of empagliflozin with sitagliptin did not have a clinically meaningful effect on the AUC(tau,ss) (GMR 103.1; 90% CI 98.9, 107.3) or C (max,ss) (GMR 108.5; 90% CI 100.7, 116.9) of sitagliptin. Empagliflozin and sitagliptin were well tolerated when given alone or in combination. Five subjects (31.3%) reported at least one adverse event (AE): three (18.8%) experienced an AE while receiving empagliflozin monotherapy and three (18.8%) while receiving sitagliptin monotherapy. No adverse events were reported during the coadministration period. No AEs were regarded as drug-related by the investigator. These results indicate that empagliflozin and sitagliptin can be coadministered without dose adjustments.
引用
收藏
页码:889 / 899
页数:11
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