Phase 3 Alzheimer's Disease Trial, Recruiting
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 have already completed a specific earlier part of this research study (called "AACM Addendum 7").
- You must have a reliable person (and a backup person) who knows you well and can speak to your daily activities, behavior, and thinking abilities.
- You must have been assigned female at birth and no longer be able to become pregnant, or have been assigned male at birth.
- You must be willing to follow local rules about contraception (birth control) during the study, if required.
Who may not be able to join:
- You have a serious or unstable health condition that the study doctor believes could affect your ability to take part.
- You are unable to have an MRI scan — for example, because you have claustrophobia (fear of enclosed spaces) or have certain metal implants or a pacemaker in your body.
- You have an abnormality or problem inside the brain (such as bleeding, inflammation, or unusual structural findings) that the study doctor thinks may put you at risk — though some specific MRI findings may be watched over time rather than automatically disqualifying you (confirm with trial site).
- You have a medical reason why you cannot receive a specific type of brain scan called a florbetapir F 18 PET scan.
- You have previously received any amyloid-targeting treatment outside of clinical trials involving the drug donanemab.
- You have taken part in another clinical trial involving a study treatment in the last 30 days, where that treatment may not be compatible with this study.
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.
Contact this trial
Principal Investigator: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST), Eli Lilly and Company
Phone: 1-317-615-4559
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
Where this trial is recruiting
Primary endpoints
Change from Baseline as Measured by Clinical Dementia Rating - Sum of Boxes (CDR-SB)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.