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临床试验/NCT02587975
NCT02587975Unknown4 期

Pharmacodynamics Study to Investigate the Effect of Evogliptin on Bone Metabolism in Healthy Volunteers

DongGuk University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2016年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
20
试验地点
1
主要终点
Serum concentration of C-terminal telopeptide after treatment in comparison with the baseline

研究概览

简要总结

This study is designed to measure the effect of evogliptin on bone metabolism in healthy volunteers.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • Postmenopausal healthy women (at least 5 years)
  • BMI 18~30 kg/m2

排除标准

  • Presence or history of hypersensitivity or allergic reactions to any drug
  • Clinically relevant abnormal medical history or present disease
  • Presence or history of drug abuse
  • Participation in other clinical trial within 2 months before dose.
  • Bood donation during 2 months or apheresis during 1 month before the study.
  • Use of a prescription medicine, herbal medicine within 2 weeks or over-the-counter medication or vitamin substances within 1 week before dose.
  • Use of any drug which can affect bone metabolism such as sex hormones or their receptor related medicine, calcitonin or parathyroid hormone related medicine, systemic corticosteroid, bisphosphate, or etc.
  • Smoking of more than 10 cigarettes/days within 3 months before first dose.
  • Use of alcohol over 21 units/weeks
  • Subject judged not eligible for study participation by investigator.

研究组 & 干预措施

Evogliptin 10 mg

Experimental

Single oral administration of 2 tablets of evogliptin 5 mg with water 250 mL

干预措施: Evogliptin (Drug)

结局指标

主要结局

Serum concentration of C-terminal telopeptide after treatment in comparison with the baseline

时间窗: Predose and 1, 2, 3, 4, 6, 14, 20, 24 h postdose on Day 1 and Day 2

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Namyi Gu

Assistant professor

DongGuk University

研究点 (1)

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