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临床试验/JPRN-jRCT1080222264
JPRN-jRCT1080222264未知Unknown

Administration study of stimulants to healthy Japanese adult females

Mitsubishi chemical Medience Corporation0 个研究点目标入组 18 人开始时间: 2013年10月28日最近更新:

试验速览

阶段
Unknown
发起方
入组人数
18

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 <= 40age old(—)
性别
Female

入选标准

  • Weight: more than 40 kg, BMI :more than 17.6 and below 26.4

排除标准

  • -Hypersensitivity to drugs,
  • -A history of alcoholism or drug addiction,
  • -Ethical or OTC pharmaceuticals administered within two weeks before scheduled administration of the study drug,
  • -Supplement, grapefruit or its products, or foods containing Hypericum perforatum
  • consumed within one week before scheduled administration of the study drug, and
  • - Not less than 200 mL of blood is collected within 30 days or not less than 400 mL of blood is collected within 90 days before scheduled administration of the study drug.
  • -A history of Graves' disease, hypertension, cardiac disease, diabetes, glaucoma, prostatomegaly, arteriosclerosis, liver disease, epilepsy, a psychiatric disorder, schizophrenia, and spasm that are not based on a cause. A person who is pregnant or has a chance of becoming pregnant.

研究者

发起方
Mitsubishi chemical Medience Corporation

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