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

被引:48
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
相关论文
共 19 条
  • [1] [Anonymous], 2009, MEDDRA INTR GUID
  • [2] [Anonymous], JAN SIT PACK INS
  • [3] Renal glucose reabsorption inhibitors to treat diabetes
    Bailey, Clifford J.
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2011, 32 (02) : 63 - 71
  • [4] Pharmacokinetic and pharmacodynamic properties of multiple oral doses of sitagliptin, a dipeptidyl peptidase-IV inhibitor: A double-blind, randomized, placebo-controlled study in healthy male volunteers
    Bergman, AJ
    Stevens, C
    Zhou, YY
    Yi, BM
    Laethem, M
    De Smet, M
    Snyder, K
    Hilliard, D
    Tanaka, W
    Zeng, W
    Tanen, M
    Wang, AQ
    Chen, L
    Winchell, G
    Davies, MJ
    Ramael, S
    Wagner, JA
    Herman, GA
    [J]. CLINICAL THERAPEUTICS, 2006, 28 (01) : 55 - 72
  • [5] Diabetes Prevalence and Therapeutic Target Achievement in the United States, 1999 to 2006
    Cheung, Bernard M. Y.
    Ong, Kwok Leung
    Cherny, Stacey S.
    Sham, Pak-Chung
    Tso, Annette W. K.
    Lam, Karen S. L.
    [J]. AMERICAN JOURNAL OF MEDICINE, 2009, 122 (05) : 443 - 453
  • [6] Friedrich C, 2011, DIABETES, V60, pA616
  • [7] Sitagliptin: Profile of a novel DPP-4 inhibitor for the treatment of type 2 diabetes
    Gallwitz, Baptist
    [J]. DRUGS OF TODAY, 2007, 43 (01) : 13 - 25
  • [8] Renal gluconeogenesis - Its importance in human glucose homeostasis
    Gerich, JE
    Meyer, C
    Woerle, HJ
    Stumvoll, M
    [J]. DIABETES CARE, 2001, 24 (02) : 382 - 391
  • [9] Empagliflozin, a novel selective sodium glucose cotransporter-2 (SGLT-2) inhibitor: characterisation and comparison with other SGLT-2 inhibitors
    Grempler, R.
    Thomas, L.
    Eckhardt, M.
    Himmelsbach, F.
    Sauer, A.
    Sharp, D. E.
    Bakker, R. A.
    Mark, M.
    Klein, T.
    Eickelmann, P.
    [J]. DIABETES OBESITY & METABOLISM, 2012, 14 (01) : 83 - 90
  • [10] Pharmacokinetics and pharmacodynamics of sitagliptin, an inhibitor of dipeptidyl peptidase IV, in healthy subjects: Results from two randomized, double-blind, placebo-controlled studies with single oral doses
    Herman, GA
    Stevens, C
    Van Dyck, K
    Bergman, A
    Yi, BM
    De Smet, M
    Snyder, E
    Hilliard, D
    Tanen, M
    Tanaka, W
    Wang, AQ
    Zeng, W
    Musson, D
    Winchell, G
    Davies, MJ
    Ramael, S
    Gottesdiener, KM
    Wagner, JA
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2005, 78 (06) : 675 - 688