Phase 2 Alzheimer's Disease Trial, Recruiting NCT06489548 Sponsor: Brigham and Women's Hospital Condition: Alzheimer's Disease
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Phase 2 Alzheimer's Disease Trial, Recruiting

NCT06489548
Recruiting Phase 2

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 have been diagnosed with early Alzheimer's disease, with memory test scores that suggest mild memory problems (your doctor can confirm this based on specific test results).
  • You are between 60 and 85 years old.
  • You are generally in good health, with no conditions likely to affect how the study is run.
  • You have been on the same medications for at least 8 weeks before the study, and this is expected to stay the same throughout the study.
  • You are not pregnant, breastfeeding, or able to become pregnant (women must be at least 2 years past menopause or have had a surgical procedure to prevent pregnancy); if you could become pregnant, your partner must use barrier contraception throughout the study.
  • A special brain scan (called an amyloid PET scan) shows a build-up of a protein called amyloid in your brain — or you have previous test results showing this (confirm with trial site).
  • You are able to understand the study and agree to take part by signing a consent form.
  • You have someone in your life (such as a family member or close friend) who knows you well and has regular contact with you, and who can participate as a study partner.

Who may not be able to join:

  • You have another significant brain or nervous system condition, such as Parkinson's disease, a history of stroke, a brain tumour, epilepsy, multiple sclerosis, or certain other neurological disorders.
  • You have serious or poorly controlled health conditions, such as uncontrolled high blood pressure, uncontrolled diabetes, or significant heart, lung, kidney, liver, or hormone-related problems.
  • You have a history of an autoimmune disease (a condition where the immune system attacks the body).
  • You have used medications that affect the immune system, or steroid treatments (including nasal sprays), in the past month.
  • You have had a major depressive episode in the past year, or have a history of bipolar disorder or schizophrenia.
  • You have had problems with alcohol or drug misuse or dependence in the past two years.
  • You have had cancer in the past 3 years.
  • Your routine blood or urine tests at screening show significant abnormalities (confirm with trial site).
  • You are currently taking part in, or have taken part in, another clinical drug trial in the past 30 days.
  • A genetic test shows a specific variation in a gene called TSPO that would affect how a particular scan works in this study (confirm with trial site).
  • You have a known sensitivity or allergy to a substance called florbetapir F18, which is used in one of the brain scans.
  • You currently have an active COVID-19 infection.
  • Your amyloid PET scan does not show a build-up of amyloid protein in the brain.
  • You have received a COVID-19 vaccine in the past 10 days, or any other vaccine in the past 7 days, at the time of your first dose in the 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.

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
Phase 2: approximately ~30% 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

Phone: 617-525-6754

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 2
Registry
ClinicalTrials.gov
Start date
16 September 2025
Est. completion
1 June 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

The number of adverse events in drug versus placebo groups.; Assessment of microglial function via PET scan using the ligand [18F]PBR06; Measure the effect of foralumab on the ratio of CD4/CD8 memory/naïve T cells biomarkers in blood

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