Safety and pharmacokinetic assessment of [11C]ketoprofen methylester in healthy volunteers
Phase 1
- Conditions
- Healthy volunteer
- Registration Number
- JPRN-UMIN000007296
- Lead Sponsor
- Division of Molecular Imaging, Institute of Biomedical Research and Innovation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 6
Inclusion Criteria
Not provided
Exclusion Criteria
1)The subject who has a peptic ulcer. 2)The subject who has blood abnormality. 3)The subject who has dysfunction in the liver / kidney. 4)The subject who has cerebrovascular disorder. 5)The subject having cardiac failure. 6)The subject with WPW or LGL syndrome, or marked bradycardia, in electrocardiogram. 7)The subject with a history of a drug or food allergy. 8)The subject who was judged by the clinical investigator to be inappropriate as a participant in this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method