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临床试验/jRCT2071210040
jRCT2071210040已完成不适用

Safety, tolerability, and pharmacokinetics of single rising oral doses of BI 474121 in healthy Japanese male subjects (doubleblind, randomised, placebo-controlled, parallel group design)

Boehringer Ingelheim0 个研究点目标入组 32 人开始时间: 2021年7月28日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
32
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
20age old over 至 45age old under(—)
性别
Male

入选标准

  • Healthy male subjects according to the assessment of the investigator, as based on a
  • complete medical history including a physical examination, vital signs (blood
  • pressure[BP], PR) including body temperature, 12-lead ECG, and clinical laboratory tests
  • at screening visit

排除标准

  • Any finding in the medical examination (including BP, PR or ECG) deviating from normal and assessed as clinically relevant by the investigator at screening visit

结局指标

主要结局

-

Percentage of subjects with drug-related adverse events

次要结局

未报告次要终点

研究者

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