Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:37 PM
Ignite Modification Date:
2025-12-24 @ 4:37 PM
NCT ID:
NCT02824666
Eligibility Criteria:
Inclusion Criteria:
* Are males \> 18 years of age and \< 50 years of age.
* BMI \<30
* Are in good health as determined by past medical history, physical examination, vital signs, electrocardiogram, and laboratory tests at screening.
* Are able to communicate well with the investigator, to understand and comply with the requirements of the study, and understand and sign the written informed consent.
* Provide informed consent for study procedures.
* Male subjects and their partners of childbearing potential must commit to the use of two methods of contraception, one of which is a barrier method for male subjects and for 90 days after the end of the study.
* Subjects must not donate sperm for the study duration and for 90 days after the end of the study.
* Willing and able to cooperate with study procedures
* A brain MRI within the past 120 days with no evidence of active or focal neurological disease that may interfere with the \[18F\]Fallypride PET data.
Exclusion Criteria:
* Use of any prescription drugs, herbal supplements, within four (4) weeks prior to Baseline imaging, and/or over-the-counter (OTC) medication, dietary supplements (vitamins included) within two (2) weeks prior to Baseline imaging. If needed (i.e. an incidental and limited need), acetaminophen is acceptable, but must be documented as a concomitant medication/significant non-drug therapy.
* Exposure to any investigational drug within the 4 weeks prior to screening visit.
* Subjects with a history of exposure to any radiation \>15 mSv/year (e.g., occupational or radiation therapy) over the past year.
* Donation or loss of 400 ml or more of blood within eight (8) weeks prior to initial dosing, or longer if required by local regulation.
* Have a history or presence of any significant cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, or neurological disorders which, in the opinion of the investigator, are capable of altering the absorption, metabolism, or elimination of drugs or posing a health risk to participate in the study.
* Have clinically significant findings on laboratory evaluations in the opinion of the investigator.
* Have clinically significant findings on ECG evaluation.
* A positive Hepatitis B surface antigen (HBsAg), Hepatitis C antibody or HIV test result.
* History of drug or alcohol abuse within the 12 months prior to screening, or evidence of such abuse as indicated by the laboratory assays conducted during the screening.
* History of tobacco product use within 3 months prior to screening, to be verified by urine cotinine screening.
* Implants such as implanted cardiac pacemakers or defibrillators, insulin pumps, cochlear implants, metallic ocular foreign body, implanted neural stimulators, CNS aneurysm clips and other medical implants that have not been certified for MRI.
* Claustrophobia that would interfere with completion of MRI and/or SPECT procedures.
* Inability to lie supine for 90 minutes at a time.
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT02824666
Study Brief:
Protocol Section:
NCT02824666