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临床试验/JPRN-jRCT2071220057
JPRN-jRCT2071220057已完成1 期

A phase I open-label study to investigate the absorption, metabolism and excretion of [14C]KDT-3594 following single oral administration in healthy adult male subjects

Shimizu Yoshitaka0 个研究点目标入组 8 人开始时间: 2022年10月16日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
8

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 <= 45age old(—)
性别
Male

入选标准

  • Healthy Japanese male
  • - Age: >18 to =<45 years old
  • - BMI: >=18.5 to <25.0 kg/m2
  • - Body weight: >=50 kg

排除标准

  • Subjects with complication or history of clinically significant hematologic, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, (including alcoholic liver disease, non-alcoholic steatohepatitis (NASH), autoimmune hepatitis, and hereditary liver disease), psychiatric, neurological, or allergic disease (including drug allergy, but excluding untreated, asymptomatic or seasonal allergy at the time of administration)

研究者

发起方
Shimizu Yoshitaka

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