首页> 外文期刊>Drug Design, Development and Therapy >Pharmacokinetics of the evogliptin/metformin extended-release (5/1,000 mg) fixed-dose combination formulation compared to the corresponding loose combination, and food effect in healthy subjects
【24h】

Pharmacokinetics of the evogliptin/metformin extended-release (5/1,000 mg) fixed-dose combination formulation compared to the corresponding loose combination, and food effect in healthy subjects

机译:依格列汀/二甲双胍缓释(5 / 1,000 mg)固定剂量组合制剂与相应的松散组合相比的药代动力学和对健康受试者的饮食影响

获取原文
           

摘要

A new fixed-dose combination formulation of evogliptin 5 mg and metformin extended-release (XR) 1,000 mg (FDC_EVO5/MET1000) was developed to improve medication adherence for type 2 diabetes mellitus. The pharmacokinetics of FDC_EVO5/MET1000 was compared to the corresponding loose combination in a randomized, open-label, crossover study in 36 healthy male subjects (Part 1), and the food effect on FDC_EVO5/MET1000 was assessed (under fasted or fed conditions) in a randomized, open-label, crossover study in 28 healthy male subjects (Part 2). Serial blood samples for pharmacokinetic analysis were collected up to 72 hours,?and pharmacokinetic parameters of evogliptin and metformin were calculated using non-compartmental methods. The geometric mean ratios (fixed-dose combination to loose combination) and 90% confidence intervals of pharmacokinetic parameters for evogliptin and metformin were all within 0.800–1.250, suggesting bioequivalent pharmacokinetic. After a single oral dose of FDC_EVO5/MET1000, food did not significantly affect evogliptin pharmacokinetic while systemic exposure of metformin was increased about 47.5% under the fed condition, which is consistent with the already established food effect on metformin XR. FDC_EVO5/MET1000 was generally well tolerated without any drug-related serious adverse events. In conclusion, FDC_EVO5/MET1000 can be substituted for the loose combination of FDC_EVO5/MET1000, providing better compliance with convenient administration.
机译:开发了一种新的固定剂量的依格列汀5毫克和二甲双胍缓释(XR)1,000毫克的组合制剂(FDC_EVO5 / MET1000),以改善2型糖尿病的药物依从性。在随机,开放标签,交叉研究中对36名健康男性受试者的FDC_EVO5 / MET1000的药代动力学与相应的宽松组合进行了比较(第1部分),并评估了其对FDC_EVO5 / MET1000的饮食效果(在禁食或进食条件下)在一项针对28位健康男性受试者的随机,开放标签,交叉研究中(第2部分)。收集长达72小时的血液样本进行药代动力学分析,并使用非房室方法计算依格列汀和二甲双胍的药代动力学参数。依格列汀和二甲双胍的几何平均比率(固定剂量组合与松散组合)和药代动力学参数的90%置信区间均在0.800-1.250之内,表明其生物等效药代动力学。单次口服FDC_EVO5 / MET1000后,食物对依福列汀的药代动力学没有明显影响,而二甲双胍的全身暴露在喂食条件下增加了约47.5%,这与已经确定的食物对二甲双胍XR的作用是一致的。 FDC_EVO5 / MET1000通常耐受良好,没有任何与药物相关的严重不良事件。总之,FDC_EVO5 / MET1000可以代替FDC_EVO5 / MET1000的松散组合,提供更好的依从性和便捷的管理。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号