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Pharmacokinetic and pharmacodynamic interaction of vildagliptin and voglibose in Japanese patients with Type 2 diabetes

机译:维格列汀和伏格列波糖在日本2型糖尿病患者中的药代动力学和药效学相互作用

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Objective: To assess the extent of pharmacokinetic and pharmacodynamic interaction between vildagliptin, a potent and selective inhibitor of dipeptidyl peptidase IV (DPP- 4) enzyme, and voglibose, an ±-glucosidase inhibitor widely prescribed in Japan, when coadministered in Japanese patients with Type 2 diabetes. Methods: In this open-label, randomized, 3-treatment, 3-period and 6-way crossover study, 24 Japanese patients with Type 2 diabetes received 50 mg vildagliptin twice daily; 50 mg vildagliptin twice daily co-administered with 0.2 mg voglibose three times daily; or 0.2 mg voglibose three times daily for 3 days in each period. Plasma concentrations of vildagliptin, DPP-4, glucagon-like peptide-1 (GLP-1), glucose, insulin, and glucagon were determined from blood samples collected at steady state. Results: Exposure to vildagliptin 50 mg (area under the concentration-time curve from 0 to 12 hours (AUCτss)) and maximum plasma concentration at steady state (Cmax,ss) was reduced by 23% and 34% respectively with coadministration of voglibose. The percentage of DPP-4 inhibition by vildagliptin remained unchanged when vildagliptin was given alone or co-administered with voglibose; maximum inhibition was 98.3 ± 1.4% (mean ± SD) for vildagliptin alone and 97.4 ± 1.1% with co-administration. Co-administration of vildagliptin and voglibose led to a greater increase in the active GLP-1 plasma concentration than did vildagliptin alone (geometric mean ratio 1.63 (90% CI, 1.30, 2.03), p = 0.0007). The combination of vildagliptin and voglibose also led to a significantly lower plasma glucose levels (p 0.0001). Conclusions: Plasma vildagliptin levels were decreased when voglibose was co-administered, although DPP-4 inhibition remained unchanged. Co-administration led to significantly better pharmacodynamic response compared with each treatment alone, including higher active GLP-1 and lower glucose levels. The results indicate that this co-administration may be beneficial in the clinical situation. Vildagliptin and voglibose treatments, alone or when co-administered, were well tolerated in Japanese patients with Type 2 diabetes.
机译:目的:在日本合并2型糖尿病的患者中,评估二肽基肽酶IV(DPP-4)的有效和选择性抑制剂维格列汀与日本广泛处方的±-葡萄糖苷酶抑制剂伏格列波糖之间的药代动力学和药效学相互作用程度。 2糖尿病。方法:在这项开放标签,随机,3治疗,3周期和6交叉研究中,24名日本2型糖尿病患者每天两次接受50 mg维格列汀治疗;每天两次50毫克维格列汀与0.2毫克伏格列波糖共同3次;或0.2 mg伏格列波糖,每天3次,每次3天。从稳定状态下采集的血液样本中测定维格列汀,DPP-4,胰高血糖素样肽-1(GLP-1),葡萄糖,胰岛素和胰高血糖素的血浆浓度。结果:与伏格列波糖合用时,维格列汀50 mg(浓度时间曲线下0至12小时的区域(AUCτss))和稳态下的最大血浆浓度(Cmax,ss)分别降低了23%和34%。当维格列汀单独使用或与伏格列波糖合用时,维格列汀对DPP-4的抑制百分比保持不变。单独使用维达列汀的最大抑制作用为98.3±1.4%(平均值±SD),并用时最大抑制作用为97.4±1.1%。与单独使用维达列汀相比,维达列汀和伏格列波糖的共同给药导致活性GLP-1血浆浓度的增加更大(几何平均比率1.63(90%CI,1.30,2.03),p = 0.0007)。维格列汀和伏格列波糖的组合还导致血浆葡萄糖水平显着降低(p <0.0001)。结论:伏格列波糖合用时血浆维达列汀水平降低,尽管DPP-4抑制作用保持不变。与单独使用每种治疗相比,共同给药可显着改善药效学反应,包括更高的活性GLP-1和更低的葡萄糖水平。结果表明这种共同给药在临床情况下可能是有益的。在日本2型糖尿病患者中,单独使用或联合使用维格列汀和伏格列波糖治疗的耐受性良好。

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