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Clinical Trials in the USA / NCT06043700
Active, not recruiting Observational

A Community-Based Screening Program to Identify Participants at High Risk for Amyloid Pathology

NCT06043700 · tracked via the Priya Life Science USA tracker
Sponsor
Eisai Limited
Phase
Observational
Started
2023-09-12
Last updated
2026-03-05

Condition(s) studied

Alzheimer's Disease

Investigational drug(s) / intervention(s)

No Intervention

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)

Trial sites (3)

FacilityCityRegionStatus
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.

View NCT06043700 on ClinicalTrials.gov ↗ ← All trials in the USA