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临床试验/jRCT2051220054
jRCT2051220054已完成不适用

Drug-drug interaction study to assess the effects of administration of K-237 on the pharmacokinetics of digoxin or rosuvastatin in healthy adult volunteers (COVID-19)

Kowa Company, Ltd.0 个研究点目标入组 10 人开始时间: 2022年7月11日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
10
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomized Controlled Trial
干预模型
Crossover Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
18age old over 至 45age old under(—)
性别
Male

入选标准

  • (1) Subject is a healthy adult male volunteer.
  • (2) Subject is between the ages of 18 and 45 years at the time of signing informed consent.
  • (3) Subject has a body mass index of 17.6 to 26.4 kg/m2 at Screening.

排除标准

  • (1) Subject has used a drug (including over-the-counter drug, vaccination) within 14 days before the administration of the study drug in the first treatment period, or those who need to use it during the study period.
  • (2) Subject has received products containing St John's wort within 4 weeks before the administration of the study drug in the first treatment period. Subject has received supplements and products containing grapefruit within 14 days before the administration of the study drug in the first treatment period.
  • (3) Subject has a current malabsorption, and those who had an operation on the gastrointestinal tract that may affect absorption (excluding appendectomy).

结局指标

主要结局

-

Plasma pharmacokinetic parameters

次要结局

未报告次要终点

研究者

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