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临床试验/jRCT2031240331
jRCT2031240331招募中不适用

Pharmacokinetic study of HP-5120

Hisamitsu Pharmaceutical Co., Inc.0 个研究点目标入组 112 人开始时间: 2024年10月17日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
112
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
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Treatment Purpose
盲法
Double Blind

入排标准

年龄范围
18age old over 至 45age old not(—)
性别
All

入选标准

  • Healthy adult Japanese males and females aged 18 or older and younger than 45 years
  • Subjects weighing 40 kg or more

排除标准

  • Subjects with or with a history of serious cardiovascular, renal, hepatic, gastrointestinal, endocrine, neuropsychiatric, dermatological, metabolic, or immunological disease
  • Subjects who received any drug within 1 week prior to administration of the investigational product
  • Subjects who took any drug considered to affect drug metabolism within 4 weeks prior to administration of the investigational product

结局指标

主要结局

-

Pharmacokinetics, Safety

次要结局

未报告次要终点

研究者

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