Fed and Fasted Single-dose Assessment of Bioequivalence of Dapagliflozin and Metformin Extended-release Fixed-dose Combination Tablets Relative to Single-component Dapagliflozin and Metformin Extended-release Tablets in Healthy Subjects

被引:11
作者
Boulton, David W. [1 ]
Chang, Ming [2 ]
Griffen, Steven C. [3 ]
Kitaura, Catia [4 ]
Lubin, Susan [2 ]
Pollack, Allyson [2 ]
LaCreta, Frank [5 ]
机构
[1] AstraZeneca, One MedImmune Way, Gaithersburg, MD 20878 USA
[2] Bristol Myers Squibb Co, Hopewell Jct, NY USA
[3] JDRF, New York, NY USA
[4] Bristol Myers Squibb Co, Sao Paulo, Brazil
[5] Bristol Myers Squibb Co, Princeton, NJ USA
关键词
bioequivalence; dapagliflozin; fixed-dose combination; metformin extended release; SGLT2; inhibitor; type 2 diabetes mellitus; ADD-ON THERAPY; INADEQUATE GLYCEMIC CONTROL; DOUBLE-BLIND; CONTROLLED-TRIAL; CLINICAL-TRIAL; TYPE-2; PHARMACOKINETICS; SULFONYLUREA; MONOTHERAPY; SITAGLIPTIN;
D O I
10.1016/j.clinthera.2015.11.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: In patients with type 2 diabetes mellitus, fixed-dose combinations (FDCs) of antihyperglycemic medications may provide complementary efficacy while reducing tablet burden and improving compliance. The aim of this study was to assess the bioequivalence and tolerability of 2 FDCs of dapagliflozin and metformin extended-release (XR) versus their individual component (IC) tablets. Methods: An open-label, balanced, randomized, 2-way crossover, 4-arm study was conducted in 129 healthy Brazilian subjects (aged 18-55 years). Two oral doses of the FDCs (5 mg dapagliflozin and 500 mg metformin XR, and 10 mg dapagliflozin and 1000 mg metformin XR) were evaluated in fed and fasted states. Findings: Under fed and fasted conditions the 5 mg dapagliflozin and 500 mg metformin XR FDC showed bioequivalence to its ICs. The 10 mg dapagliflozin and 1000 mg metformin XR FDC was bioequivalent to its ICs in fed subjects. Although AUC for the 10 mg dapagliflozin and 1000 mg metformin XR FDC was bioequivalent in fasted subjects, the Gina), for metformin was not bioequivalent to its ICs in fasted subjects (upper 90% CI was 127.5%, and thus outside the 80%-125% bioequivalence interval). The small increase in the fasted state is not considered clinically meaningful due to the small magnitude of the difference (9.2%), the lack of metformin C-max being associated with efficacy or tolerability concerns, and the fasted state not being the recommended state for dosing of metformin XR. The safety profile and tolerability of the FDCs were similar to those of their ICs and no deaths or serious adverse events were reported. Implications: Both FDCs of dapagliflozin and metformin XR were bioequivalent to their ICs in fed and fasted subjects, except for the metformin C-max from the 10 mg dapagliflozin and 1000 mg metformin XR FDC in fasted subjects. These data support the use of a dapagliflozin and metformin XR FDC in patients with type 2 diabetes mellitus. (C) 2016 Elsevier HS Journals, Inc. All rights reserved.
引用
收藏
页码:99 / 109
页数:11
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