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Administration study as a part of research toward the development of detection method for erythropoietin preparations in biological samples

Not Applicable
Conditions
ot applicable
Registration Number
JPRN-jRCT1080221264
Lead Sponsor
Mitsubishi chemical Medience Corporation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

Weight: over 50 kg, BMI: under 18.5 and below 25

Exclusion Criteria

-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.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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