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Evaluation of [18F]MNI-1126 as an Imaging Marker for Synaptic Density Loss

Phase 1
Completed
Conditions
Healthy Volunteers
Parkinson Disease
Alzheimer Disease
Interventions
Registration Number
NCT03587649
Lead Sponsor
Invicro
Brief Summary

The primary objective of this protocol is to examine \[18F\]MNI-1126 as a tool to assess synaptic density loss.

Detailed Description

The primary objective of this protocol is to examine \[18F\]MNI-1126 as a tool to assess synaptic density loss.The specific objectives are:

* Examine \[18F\]MNI-1126 as a tool to assess synaptic density loss.

* To measure the dynamic uptake and washout of \[18F\]MNI-1126 in the brain using positron emission tomography (PET) in subjects with AD, PD, and healthy volunteers.

* To measure blood metabolites of \[18F\]MNI-1126 and perform kinetic modeling to assess its ability to measure synaptic density loss in the brain using the tracer plasma concentration or a reference region as indirect input.

* To acquire safety data following injection of \[18F\]MNI-1126.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
12
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
[18F]MNI-1126[18F]MNI-1126To measure the dynamic uptake and washout of \[18F\]MNI-1126 in the brain using positron emission tomography (PET) in subjects with AD, PD, and healthy volunteers.
Primary Outcome Measures
NameTimeMethod
Regions in the VOI template will be used to quantify the regional tracer uptake and used for comparison of potential uptake differences across the different groups.1 year

Descriptive statistics will be applied to describe the tau deposition by region as measured by \[18F\]MNI-1126.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Invicro

🇺🇸

New Haven, Connecticut, United States

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