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临床试验/NL-OMON49451
NL-OMON49451已完成不适用

A single-center, open-label study to investigate the absorption, distribution, metabolism and excretion (ADME) of HDM201 (Siremadlin) after a single oral dose of 25 mg [14C]HDM201 in healthy subjects - [14C]HDM201

ovartis Pharma AG0 个研究点目标入组 5 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
5

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
18 至 99(—)

入选标准

  • Healthy males and/or females age 18 to 54 years included
  • Weighy at least 55 kg and no more than 120 kg
  • BMI 18.0 - 30 kg/m2

排除标准

  • Females of childbearing potential (WOCBP).
  • Exposure to radiation at a level of 0.1 to1.0 mSv over the past year, 1.1 to
  • 2.0 mSv over the past 2 years, or 2.1 to 3.0 mSv over the past 3 years, etc.,
  • e.g., due to systemic administration of radioactive substances, or to external
  • irradiation (e.g., by x-rays) for diagnostic,
  • therapeutic, job-related, or research purposes.
  • Use of other investigational drugs within 5 half-lives, or within 6 months (in
  • case of therapeutics with expected long half-lives such as immunoglobulin G
  • antibodies), or within 30 days prior to dosing (for
  • small molecule drugs with daily dosing scheme), or longer if required
  • by local regulations.
  • Any surgical or medical condition which might significantly alter the ADME of
  • drugs, or which may jeopardize the subject in case of participation in the
  • Has absence of regular defecation pattern (subjects with a mean defecation
  • frequency of less than once per 2 days or chronic diarrhea).
  • Positive for Hepatitis B surface antigen (HBsAg), Hepatitis C virus (HCV),
  • and/or human immunodeficiency virus (HIV).
  • Smokers (use of tobacco/nicotine products in the previous 3 months).
  • History or presence of clinically significant ECG abnormalities or a family
  • history or presence of prolonged QT-interval syndrome.

研究者

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