Assessment of the Biodistribution and Safety of [18F]MNI-... | NCT03142724

NCT03142724

Protocol Section

Identification Module

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Status Module

Description Module

Label	Type	Description	Intervention Names
[18F]MNI-968	Experimental	To assess the safety and tolerability and to determine the radiation dosimetry of [18F]MNI-968.	Drug: [18F]MNI-968

Name	Type	Description	Arm Group Labels	Other Names
[18F]MNI-968	Drug	Healthy volunteers recruited for the study will undergo a single [18F]MNI-968 injections and PET scans.	[18F]MNI-968

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Whole body tomographic PET images will be obtained for 6 healthy volunteers, and reviewed visually for assessment of body organ distribution of radioactivity.	Volumes of interest (VOI) will be placed on the visually identified source organs, and subsequently used for all the study PET frames. Activity within these volumes of interest is expressed in units of total radioactivity (kBq). Radioactivity will be corrected for body attenuation, but not for decay, and time activity data (TAC) generated for each source organ.	2 Months

Eligibility Module

Eligibility Criteria

Inclusion Criteria

The participant is 18 to 55 years old.
Written informed consent must be obtained before any assessment is performed.
Female subjects must be documented by medical records or physician's note to be either surgically sterile (by means of hysterectomy, bilateral oophorectomy, or tubal ligation) or post-menopausal for at least 1 year or, if they are of child-bearing potential, must commit to use a barrier contraception method for the duration of the study.
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 for the study duration.
Male subjects must not donate sperm for the study duration.
Willing and able to cooperate with study procedures

Exclusion Criteria

The subject has a clinically significant abnormal laboratory value and/or clinically significant unstable medical or psychiatric illness.
The subject is a currently exposed to nicotine products or had regular nicotine exposure within a six month period, to be verified by urine cotinine screening.
History of drug or alcohol abuse within 12 months prior to screening, or evidence of such abuse as indicated by the laboratory assays conducted during the screening visit.
The subject has evidence of clinically significant gastrointestinal, cardiovascular, hepatic, renal, hematological, neoplastic, endocrine, neurological, immunodeficiency, pulmonary, or other disorder or disease.
The subject has any disorder that may interfere with drug absorption, distribution, metabolism, or excretion.
Prior participation in other research protocols or clinical care in the last year in addition to the radiation exposure expected from participation in this clinical study, such that radiation exposure does not exceed the effective dose of 50 mSv, equivalent with the acceptable annual limits established by the US Federal Guidelines.
Pregnancy or women who are breastfeeding, lactating or nursing.
Unsuitable veins for repeated venipuncture.
History of immunodeficiency diseases, including a positive HIV test result
A positive Hepatitis B surface antigen (HBsAg) or Hepatitis C antibody test result.