跳至主要内容
临床试验/JPRN-jRCT2071220011
JPRN-jRCT2071220011已完成1 期

Clinical Pharmacology Study of NS-580 in Healthy female subjects (Phase I Study)

Higashioka Masaya0 个研究点目标入组 64 人开始时间: 2022年5月27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
64

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 < 45age old(—)
性别
Female

入选标准

  • 1) Provided written informed consent
  • 2) Japanese female subjects
  • 3) Body mass index (BMI) >=17.6 and <25.0 kg/m2 at the time of screening tests and hospitalization

排除标准

  • 1) Sublects who are pregnant, may become pregnant, or wish to become pregnant during the trial period
  • 2) Subjects who are breastfeeding
  • 3) Subjects who have not confirmed a regular menstrual cycle at the time of screening test
  • 4) Subjects who are irregular bleeding

研究者

发起方
Higashioka Masaya

相似试验