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A fixed-dose combination tablet of gemigliptin and metformin sustained release has comparable pharmacodynamic, pharmacokinetic, and tolerability profiles to separate tablets in healthy subjects

机译:吉格列汀和二甲双胍缓释固定剂量组合片剂具有与健康受试者中分开的片剂相当的药效学,药代动力学和耐受性特征

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Background: In type 2 diabetes mellitus, fixed-dose combination (FDC) can provide the complementary benefits of correction of multiple pathophysiologic defects such as dysfunctions in glycemic or metabolic control while improving compliance compared with separate tablets taken together. The objective of the study reported here was to compare the pharmacodynamic (PD), pharmacokinetic (PK), and tolerability profiles of gemigliptin and extended-release metformin (metformin XR) between FDC and separate tablets.Methods: A randomized, open-label, single-dose, two-way, two-period, crossover study was conducted in 28 healthy male volunteers. Two FDC tablets of gemigliptin/metformin 25/500 mg or separate tablets of gemigliptin (50 mg ×1) and metformin XR (500 mg ×2) were orally administered in each period. Serial blood samples were collected up to 48 hours post-dose to determine dipeptidyl peptidase 4 (DPP-4) activity using spectrophotometric assay and concentrations of gemigliptin and metformin using tandem mass spectrometry. Geometric mean ratios (GMRs) of FDC to separate tablet formulations and their 90% confidence intervals (CIs) were calculated to compare the PD and PK parameters between the two formulations. Tolerability was assessed throughout the study.Results: The plasma DPP-4 activity–time curves of the FDC and the separate tablets almost overlapped, leading to a GMR (90% CI) of the FDC to separate tablets for the plasma DPP-4 activity and its maximum inhibition of 1.00 (0.97–1.04) and 0.92 (0.82–1.05), respectively. Likewise, all of the GMRs (90% CIs) of FDC to separate tablets for the area under the plasma concentration–time curve and maximum plasma concentration of gemigliptin and metformin fell entirely within the conventional bioequivalence range of 0.80–1.25. Both the FDC and separate tablets were well tolerated.Conclusion: The PD, PK, and tolerability profiles of gemigliptin and metformin XR in FDC and separate tablets were found to be comparable. The FDC tablet of gemigliptin and metformin sustained release can be a convenient therapeutic option in patients with type 2 diabetes mellitus requiring a combination approach.
机译:背景:在2型糖尿病中,固定剂量联合用药(FDC)与单独使用的多种片剂相比,可提供纠正多种病理生理缺陷(如血糖控制或代谢控制功能障碍)的补充益处,同时提高依从性。本研究报告的目的是比较FDC和独立片剂之间吉吉利汀和缓释二甲双胍(metformin XR)的吉吉利汀和药代动力学(PD),药代动力学(PK)和耐受性特征。方法:随机,开放标签,在28位健康的男性志愿者中进行了单剂量,双向,两期,交叉研究。在每个时期内口服两片Fig吉吉利汀/二甲双胍25/500 mg或单独的吉吉利汀(50 mg×1)和二甲双胍XR(500 mg×2)。给药后长达48小时收集系列血样,使用分光光度法测定二肽基肽酶4(DPP-4)的活性,并使用串联质谱法测定吉吉利汀和二甲双胍的浓度。计算了FDC与单独片剂的几何平均比(GMR)及其90%置信区间(CIs),以比较两种制剂之间的PD和PK参数。在整个研究过程中评估了耐受性。结果:FDC和单独的片剂的血浆DPP-4活性-时间曲线几乎重叠,导致FDC的GMR(90%CI)分离出具有血浆DPP-4活性的片剂其最大抑制分别为1.00(0.97–1.04)和0.92(0.82–1.05)。同样,在血浆浓度-时间曲线以及吉吉利汀和二甲双胍的最大血浆浓度下,FDC分离片剂的所有GMR(90%CI)完全落在传统生物等效性范围0.80-1.25之间。结论:吉非列汀和二甲双胍XR在FDC和单独的片剂中的PD,PK和耐受性特征均具有可比性。吉格列汀和二甲双胍缓释的FDC片剂可以作为需要联合治疗的2型糖尿病患者的便捷治疗选择。

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