Phase 1 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:
- People who have experienced a gradual and ongoing decline in memory that has been noticed by themselves or someone who knows them well, lasting 6 months or more, consistent with a diagnosis of Alzheimer's disease dementia
- People whose score on a standard memory and thinking test (called the Mini Mental State Examination) falls between 16 and 24 out of 30
- People whose blood test results meet specific protein markers related to Alzheimer's disease, as defined by the organisation running the trial (confirm with trial site)
- People whose body weight relative to their height (BMI) is between 17 and 32 at the time of screening
- Women who are not able to become pregnant, and men who are willing to use effective contraception for the duration of the study
- People who have adequate reading ability, vision, and hearing to complete study tasks throughout the trial
- People who have at least one, and up to two, support persons (such as a family member or carer) who spend at least 10 hours per week with them
Who may not be able to join:
- People for whom an MRI scan is not safe, including those with claustrophobia or certain metal implants or a cardiac pacemaker
- People whose screening MRI scan shows significant abnormal findings
- People with a history of suicidal behaviour, a past suicide attempt, or current thoughts of suicide
- People with a history of severe or ongoing allergic reactions, hypersensitivity to vaccines or immunoglobulins, two or more serious drug allergies, intolerance to topical corticosteroids, or severe reactions after receiving treatments
- People with a current serious or unstable medical condition affecting the liver, kidneys, digestive system, lungs, heart, nervous system (other than Alzheimer's disease), mental health, hormones, immune system, or blood
- People who are currently being treated with, or have received, a type of biological medicine called a monoclonal antibody within the past 3 months or within 5 half-lives of that medicine (whichever period is longer)
- People for whom a lumbar puncture (a procedure to collect fluid from around the spine) would not be medically appropriate (confirm with trial site)
- People who are currently taking part in another clinical study involving an experimental treatment or medical research that may conflict with this trial
- People who are currently using therapies that target amyloid (a protein associated with Alzheimer's disease); people who used such therapies more than one year ago may be considered, at the discretion of the treating doctor and the trial sponsor
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
Australian sites
+61 482 130 622
+617 54563872
+613 9496 2388
+612 8566 1500
0298122956
0437 498 365
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
6 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Change from Baseline in Cerebrospinal Fluid (CSF) Neurofilament Light Chain (NfL)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.