Development of Diagnostic Imaging of Malignant Tumor using New PET Probe AIB
- Conditions
- Malignant neoplasmsD009369
- Registration Number
- JPRN-jRCTs031210540
- Lead Sponsor
- Tamura Kentaro
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Male
- Target Recruitment
- 10
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
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Safety of [11C]AIB in human subjects <br>Radiation dosimetry of [11C]AIB in human subjects
- Secondary Outcome Measures
Name Time Method Pharmacokinetics of [11C]AIB