Phase 1 Alzheimer's Disease Trial, Recruiting NCT05606341 Sponsor: NYU Langone Health Condition: Alzheimer's Disease
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Phase 1 Alzheimer's Disease Trial, Recruiting

NCT05606341
Recruiting Phase 1

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 are between 65 and 85 years of age
  • People who have been diagnosed with mild cognitive impairment or mild dementia due to Alzheimer's disease, based on specific 2018 diagnostic guidelines
  • People who score 17 or higher on a standard memory and thinking test called the Montreal Cognitive Assessment (MoCA)
  • People who have had a brain scan (called a PET amyloid scan, such as a Florbetaben scan) that showed amyloid deposits, performed within one year of joining the study
  • People who are able to give their own consent or agreement to participate
  • People who are willing and able to take part in all study-related activities and appointments
  • People who have a reliable support person (such as a family member or close friend) who knows them well, has regular contact with them, and is available to attend clinic visits or be reached by phone

Who may not be able to join:

  • People with a history of psychiatric conditions — such as hallucinations, major depression, thoughts of suicide, or delusions — that could interfere with completing study activities (as assessed by the lead doctor)
  • People with a history of autoimmune disorders, conditions where the immune system attacks the body, severe asthma, or other serious infections or systemic illnesses (as assessed by the lead doctor)
  • People who have used corticosteroids (steroid medications) or immune-suppressing drugs in the 30 days before joining the study
  • People who have previously had their spleen removed
  • People who have reduced kidney function
  • People who have used chloroquine (a medication sometimes used for malaria or autoimmune conditions) within 8 weeks before joining the study
  • People who are unable to have an MRI scan
  • People who have had a mini-stroke (TIA), stroke, or seizures within the 12 months before screening
  • People with any other neurological condition — apart from Alzheimer's disease — that could be affecting their thinking or memory, including possible effects from long COVID (as assessed by the lead doctor)
  • People who are currently participating in another Alzheimer's disease clinical trial that involves an investigational treatment
  • People who are currently taking blood-thinning (anticoagulant) medication
  • People who are currently taking certain medications that are processed by a specific liver enzyme called CYP1A2 (confirm with trial site for a list of affected medications)
  • People who have been exposed to COVID-19 infection within the past 14 days, or who have had recent symptoms that may be related to COVID-19 within the past 14 days

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 20 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: Arjun Masurkar, MD, NYU Langone Medical Center

Phone: 212-263-0771

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
13 March 2023
Est. completion
1 November 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of Patient-Reported Adverse Events (AEs); Percentage of Participants with Rheumatoid Factor (RF) Confirmed by Autoimmunity Marker Screening Test Result; Percentage of Participants with Antinuclear Antibody (ANA) Confirmed by Autoimmunity Marker Screening Test Result; Percentage of Participants with Antineutrophil Cytoplasmic Antibody (ANCA) Confirmed by Autoimmunity Marker Screening Test Result; Percentage of Participants with Amyloid-Related Imaging Abnormalities-Haemosiderin (ARIA-H) Confirmed by Magnetic Resonance Imaging (MRI); Percentage of Participants with Amyloid-Related Imaging...

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: 20 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