Alzheimer's Disease Trial, Recruiting NCT06547099 Sponsor: Washington University School of Medicine Condition: Alzheimer's Disease
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Alzheimer's Disease Trial, Recruiting

NCT06547099
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You must be at least 60 years old
  • 80% of new participants enrolled through the clinic will have symptoms such as forgetfulness, mild memory problems, mild dementia, or Alzheimer's disease, as noted in their medical records or by their doctor
  • People already taking part in a related study called SEABIRD are also welcome to join, whatever their memory or thinking abilities

Who may not be able to join:

  • People who are unable to do basic daily tasks on their own — such as eating, bathing, getting dressed, moving around, or using the toilet — because of memory or thinking problems
  • People who have uncontrolled hepatitis B, hepatitis C, or HIV at the time their blood is collected
  • People who are currently taking a medication designed to treat or slow the progression of Alzheimer's disease
  • People who have had a blood transfusion within the last three months
  • People who are unwilling or unable to take part in all of the study activities

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Randall Bateman, MD, Washington University School of Medicine

Phone: 314-747-4857

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
14 August 2024
Est. completion
1 December 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Area under the curve (AUC) of plasma amyloid-beta 42/40 in predicting amyloid PET status; Area under the curve (AUC) of plasma %p-tau217 in predicting amyloid PET status; Area under the curve (AUC) of plasma p-tau217 in predicting tau PET status; Area under the curve (AUC) of plasma p-tau205 in predicting tau PET status; Area under the curve (AUC) of plasma neurofilament light in predicting tau PET status; Area under the curve (AUC) of plasma %p-tau205 in predicting clinical diagnosis; Area under the curve (AUC) of plasma %p-tau217 in predicting clinical diagnosis; Area under the curve (AUC) o...

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov