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临床试验/JPRN-jRCT2031210090
JPRN-jRCT2031210090已完成1 期

Repeated dose study of NPC-25 in healthy adult male volunteers. - NPC-25-2

Kitamura Motohiro0 个研究点目标入组 48 人开始时间: 2021年5月13日最近更新:

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
48

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 < 35age old(—)
性别
Male

入选标准

  • (1) Subjects aged from 20 to 35 years healthy adult Japanese male
  • (2) Subjects with BMI (body mass index:weight (kg) / height (m) 2 ) of 18.5 or more and less than 25.0
  • (3) Subjects whose serum zinc concentration at the time of screening test (within 4 weeks before the start of
  • the clinical trial) is less than 100 microgram / dL
  • (4) Signature of the subjects on the Informed Consent Form

排除标准

  • (1) Drug addicts, alcohol addicts.
  • (2) Subjects with a history of visceral disease or surgery that may affect drug metabolism or excretion.
  • (3) Subjects who can not keep drinking or smoking cessation during hospitalization.
  • (4) Subjects with allergies or hypersensitivity to zinc containing preparations (including supplements).
  • (5) Subjects who have taken zinc containing preparations or zinc containing supplements that are prohibited
  • from being used in combination within 4 weeks before the start of the clinical trial.
  • (6) Subjects who participated in other clinical trials within 12 weeks before the start of the clinical trial.
  • (7) Subjects whose serum copper concentration deviates from the normal standard value range.
  • (8) Subjects who donated 400 mL or more within 12 weeks, 200 mL or more within 4 weeks, and subjects
  • who donated component blood within 2 weeks before the start of the clinical trial.
  • (9) Other patients considered inappropriate by the investigators for inclusion in the study.

研究者

发起方
Kitamura Motohiro

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