Administration study of stimulants to healthy Japanese adult females
- Conditions
- ot applicable
- Registration Number
- JPRN-jRCT1080222264
- Lead Sponsor
- Mitsubishi chemical Medience Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Sex
- Female
- Target Recruitment
- 18
Weight: more than 40 kg, BMI :more than 17.6 and below 26.4
-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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method