跳至主要内容
临床试验/NL-OMON48072
NL-OMON48072已完成不适用

A study evaluating the pharmacokinetics, safety and tolerability of OP2113 administered intravenously in healthy volunteers and a marketed formulation administered orally - OP2-CS-001 OP2 Drugs

OP2 Drugs0 个研究点目标入组 12 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
12

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 male and female subjects aged between 18 and 65 years (inclusive) with
  • a body mass index (BMI) of *18.0 kg/m2 and * 30.0 kg/m2 (inclusive) at
  • Further inclusion criteria can be found in the protocol section 8.4.1

排除标准

  • Relevant prior or ongoing medical condition that, in the Investigator*s
  • opinion, could adversely affect the safety of the subject.
  • History of clinically-significant hypersensitivity to any of the study drugs,
  • excipients or materials used to administer the study medication.
  • Further exclusion criteria can be found in the protocol section 8.4.2

研究者

发起方
OP2 Drugs

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