No Intervention: No treatment intervention will be administered.
Study summary
The primary purpose of this study is to identify participants with or without symptoms of Alzheimer's Disease (AD) that are at high risk for brain amyloid pathology using blood-based biomarkers.
Eligibility
Sex
ALL
Min age
50 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria:
1. Male or female, age 50 to 80 years inclusive, at the time of informed consent
\- Those 50 to 64 years of age must have 1 of the following risk factors confirmed prior to blood sample collection:
* First degree relative with dementia onset before age 75,
* Known before screening to have at least 1 Apolipoprotein E4 (APOE4) allele, or
* Known before screening to have elevated brain amyloid according to previous positron emission tomography (PET), cerebrospinal fluid (CSF), or blood testing
2. Provide written informed consent
3. Willing and able to comply with all aspects of the protocol
4. Willing to be referred to a clinical site if the assessment results meet the criteria
Exclusion Criteria:
1. Known uncontrolled medical conditions (example, cardiac, respiratory, gastrointestinal, psychiatric, renal disease, malignant neoplasm)
2. Participation in an interventional clinical trial study at the time of consent
Primary outcome measure(s)
Number of Participants With Low, Medium, and High Amyloid Pathology — At Screening on Day 1 Number of participants with low, medium, and high amyloid pathology will be estimated.
Trial sites (3)
Facility
City
Region
Status
Eisai Site #3
Clermont
Florida
Eisai Site #1
Lady Lake
Florida
Eisai Site #2
District Heights
Maryland
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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