Phase 1 Alzheimer's Disease Trial, Recruiting NCT07598370 Sponsor: Eli Lilly and Company Condition: Alzheimer's Disease
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Phase 1 Alzheimer's Disease Trial, Recruiting

NCT07598370
Recruiting Phase 1 🇦🇺 Australian site

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.

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 16 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Flinders Medical Centre, Adelaide,
+61 482 130 622
University of the Sunshine Coast Clinical Trial Centre, Birtinya,
+617 54563872
Austin Health - Heidelberg Repatriation Hospital, Ivanhoe,
+613 9496 2388
Southern Neurology, Kogarah,
+612 8566 1500
Macquarie University Hospital, Macquarie University,
0298122956
The Alfred, Melbourne,
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

Status
Recruiting
Phase
Phase 1
Registry
ClinicalTrials.gov
Start date
21 May 2026
Est. completion
1 May 2027

Where this trial is recruiting

🇦🇺 Australia 🇸🇬 Singapore

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?

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: 16 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