跳至主要内容
临床试验/JPRN-jRCT2071200100
JPRN-jRCT2071200100已完成1 期

Investigation of safety, tolerability and pharmacokinetic properties of single subcutaneous doses of NNC0194-0499 in Japanese and non-Asian male subjects(NN9500-4663)

Sudoh Yuki0 个研究点目标入组 42 人开始时间: 2021年2月19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
42

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
>= 20age old 至 <= 55age old(—)
性别
Male

入选标准

  • 1. For Japanese subjects only, both parents of Japanese descent. For non-Asian subjects only, both parents of non-Asian descent.
  • 2. Body mass index (BMI) between 23.0 and 34.9 kg/m2 (both inclusive). Overweight should be due to excess adipose tissue, as judged by the investigator.
  • 3. Body weight >= 60 kg.
  • 4. Considered by the investigator to be generally healthy based on the medical history, physical examination, and the results of vital signs, ECG, and clinical laboratory tests performed during the screening visit.

排除标准

  • Any disorder which in the opinion of investigator might jeopardise subject safety or compliance with the protocol.

研究者

发起方
Sudoh Yuki

相似试验

Investigation of safety, tolerability and... | 临床试验