JPRN-jRCTs031210134Completed未知
Safety and pharmacokinetic study of a new PET probe [18F]FEDAC in healthy adults
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Tamura Kentaro
- Enrollment
- 10
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- >= 20age old to < 65age old (—)
- Sex
- Male
Inclusion Criteria
- •1. Healthy male subjects aged 20 or older and under 65 at the time of informed consent
- •2. Subjects who provide written informed consent
- •3. Subjects with BMI of less than 25
Exclusion Criteria
- •1. Subjects who have severe or progressive complications.
- •2. Subjects who have obvious abnormalities in physical and laboratory examinations after obtaining the informed consent
- •3. Subjects who have past history of severe drug hypersensitivity
- •4. Subjects with drug or alcohol addiction
- •5. Subjects who smoke
- •6. Subjects who have received medication or used vitamins, herbal medicines, or supplements within 14 days prior to their visit
- •7. Subjects who are claustrophobic
- •8. Subjects who have undergone an examination with radiation exposure for the purpose of medical treatment (X-ray, CT, PET, DEXA, etc.) within the past 12 months, or for the purpose of research within the past 6 months. Chest X-rays conducted as part of the annual medical check are excluded.
- •9. Subjects who are considered to be inappropriate to participate in this study.
Investigators
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