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临床试验/NCT02954822
NCT02954822已完成1 期

A Randomized, Open-label, Multiple Dosing, Cross-over Clinical Trial to Investigate the Pharmacokinetic/Pharmacodynamic Drug-drug Interaction of Evogliptin 5mg and Glimepiride 4mg After Oral Administration in Healthy Male Subjects

Dong-A ST Co., Ltd.1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2016年11月14日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
36
试验地点
1
主要终点
AUCτ,ss for Evogliptin and Glimepiride

研究概览

简要总结

A randomized, open-label, multiple dosing, three treatment, three period, two sequence clinical trial to investigate the pharmacokinetic/pharmacodynamic drug-drug interaction of evogliptin 5 mg and glimepiride 4 mg after oral administration in healthy male subjects

详细描述

A randomized, open-label, multiple-dose, three-treatment, three-period, two-sequence, crossover study

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
19 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy Male Volunteers (Age: 19~45years)
  • 55<Body Weight<90, 18<BMI<27
  • FPG: 70-125 mg/dL

排除标准

  • galactose intolerance, Lapp lactase deficiency, glucose-galactose malabsorption
  • Clinically significant Medical History
  • Allergy or Drug Hypersensitivity
  • AST(SGOT), ALT(SGPT) > Upper Normal Range*1.5, eGFR<80 mL/min
  • Drink during clinical trial period
  • Smoking during clinical trial period
  • Grapefruit/Caffeine intake during clinical trial period
  • No Contraception

研究组 & 干预措施

(Group A)

Experimental

Evogliptin→Evogliptin+Glimepiride→Glimepiride

干预措施: Evogliptin→Evogliptin+Glimepiride→Glimepiride (Drug)

(Group B)

Experimental

Glimepiride→Evogliptin→Evogliptin+Glimepiride

干预措施: Glimepiride→Evogliptin→Evogliptin+Glimepiride (Drug)

结局指标

主要结局

AUCτ,ss for Evogliptin and Glimepiride

时间窗: 3 weeks

area under the concentration-time curve

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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