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

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• 作者：David W. Boulton ; PhD¹ ; ^{david.boulton2@astrazeneca.com" class="auth_mail" title="E-mail the corresponding author} ; Ming Chang ; PhD² ; Steven C. Griffen ; MD³ ; Catia Kitaura ; PharmB⁴ ; Susan Lubin ; MA² ; Allyson Pollack ; MA² ; Frank LaCreta ; PhD⁵
• 关键词：bioequivalence ; dapagliflozin ; fixed-dose combination ; metformin extended release ; SGLT2 inhibitor ; type 2 diabetes mellitus
• 刊名：Clinical Therapeutics
• 出版年：2016
• 出版时间：1 January 2016
• 年：2016
• 卷：38
• 期：1
• 页码：99-109
• 全文大小：238 K

文摘

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.

c_2">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.

c_3">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 C_max 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.

c_4">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.