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Administration study to healthy adult female as part of reserach toward the development of detection method for testosterone doping

Administration study to healthy adult female as part of reserach toward the development of detection method for testosterone doping

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1080221545
Enrollment
10
Registered
2011-08-15
Start date
2011-08-15
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

investigational material(s) Generic name etc : Enarmon Depot Intermuscular injection 125mg INN of investigational material : Therapeutic category code : 246 Androgen preparations Dosage and Administr

Sponsors

Mitsubishi chemical Medience Corporation
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: BMI: more than 17.6 and below 26.4

Exclusion criteria

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.

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026