biodistribution, dosimetry, healthy volunteers
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age between 18-65 years; 2. Good physical health evaluated by medical history, physical (including neurological) examination and screening laboratory tests; 3. Written informed consent of each subject.
Exclusion criteria
Exclusion criteria: 1. Any clinical significant abnormality of any clinical laboratory test; 2. Any subject who has received any investigational medication within 30 days prior to the start of this study, or who is scheduled to receive an investigational drug; 3. Major psychiatric or neurological disorder; 4. History of alcohol and/or drug abuse (DSM-IV criteria); 5. History of coagulation problems; 6. Any sign of cardiovascular disease; 7. Current use of any medication, other than contraceptive medication; 8. Breast feeding; 9. Pregnancy; 10. Unable to understand or read the Dutch language.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Biodistribution and dosimetry of [11C]Laniquidar in healthy volunteers. | — |
Secondary
| Measure | Time frame |
|---|---|
| Metabolic profile of [11C]Laniquidar in humans. | — |
Contacts
P.O.Box 7057