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NCT06653153

NCT06653153
Active, Not Recruiting Phase 3 🇦🇺 Australian site

Who may be able to join

Who might be able to join this trial:

  • You have had a specific blood or fluid test (measuring a protein called phosphorylated tau) that suggests the presence of Alzheimer's-related changes in the brain.
  • You have a reliable person (such as a family member or close friend) who knows you well and can report on your daily activities and thinking abilities, plus a backup person who can do the same.
  • You are able to see, hear, and read well enough to complete memory and thinking tests at the start of the study.
  • Your score on a standard memory and thinking test (called the MMSE) shows no or very minimal cognitive problems.
  • Your score on a daily functioning questionnaire (called the FAQ) shows no or very minimal difficulty with everyday tasks.
  • If you are already taking medication for Alzheimer's symptoms, your dose has been the same for at least 30 days before joining the study.

Who may not be able to join:

  • You have been diagnosed with dementia or another significant brain or neurological condition that affects thinking and memory.
  • You have a serious or unstable health condition that the study doctor believes could affect the study results.
  • You have a history of cancer that the study doctor considers at high risk of coming back.
  • You have a history of significant or severe allergic reactions to multiple medications or drugs.
  • You have an abnormal lab test result or other health finding that the study doctor believes could be harmful to you or affect the study.
  • You have any reason you cannot safely have an MRI scan (for example, certain metal implants).
  • Your MRI scan, reviewed by a central specialist, does not meet the study's required standards.
  • You have ever previously received a passive anti-amyloid immunotherapy treatment (a specific type of Alzheimer's antibody treatment) (confirm with trial site).
  • You have previously received an active Alzheimer's vaccine (Aβ immunization) in another 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.

Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.

Trial details

Status
Active, Not Recruiting
Phase
Phase 3
Sponsor
Eli Lilly and Company
Registry
clinicaltrials_gov
Start date
24 October 2024
Est. completion
1 April 2029

Where this trial is recruiting

🇦🇺 Australia 🇨🇦 Canada 🇨🇳 China 🇯🇵 Japan Puerto Rico 🇰🇷 South Korea 🇪🇸 Spain 🇹🇼 Taiwan 🇬🇧 United Kingdom 🇺🇸 United States

16 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Time to Clinically Meaningful Progression as Measured by Clinical Dementia Rate Scale (CDR)

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: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov