跳至主要内容
临床试验/EUCTR2011-003433-33-Outside-EU/EEA
EUCTR2011-003433-33-Outside-EU/EEA进行中(未招募)不适用

A Single Dose Biocomparison Study to Assess two Pediatric Formulations of MK-8669 to the Provisional Market Formulation in Healthy Subjects - A Single Dose Study to Assess the Biocomparison of MK-8669 in Subjects

Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.0 个研究点目标入组 21 人开始时间: 2011年7月21日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
21

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Male

入选标准

  • Healthy, male subjects, aged 18 to 45 years.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 21
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Subject has a history of any illness that, in the opinion of the study investigator, might confound the results of the study or poses an additional risk to the subject by their participation in the study.

研究者

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