Status:

COMPLETED

Safety and Feasibility of Dasatinib and Quercetin in Adults at Risk for Alzheimer's Disease

Lead Sponsor:

Lewis Lipsitz

Conditions:

Aging

Eligibility:

All Genders

65+ years

Phase:

PHASE1

PHASE2

Brief Summary

The purpose of this pilot study is to demonstrate the safety and feasibility of administering intermittent doses of Dasatinib and Quercetin (D+Q) in older adults at risk of Alzheimer's disease (AD). T...

Detailed Description

The investigators will conduct a 12-week single arm, open label, pre-post pilot study in 12 adults aged 65 or older with slow gait speed (\<1.0 m/sec) and Mild Cognitive Impairment (MCI, defined as a ...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • Men and women \>/= 65 years
  • Ambulatory,
  • Community dwelling,
  • Slow gait speed (\<1 m/second),
  • Mild Cognitive Impairment (Telephone MoCA score \<21, which is indicative of cognitive impairment)
  • Exclusion Criteria, or as per clinical judgment:
  • Telephone MoCA score \<10 points
  • Unwilling to take study medications or follow study protocol
  • Inability to independently perform Katz Activities of Daily Living (ADLs),
  • Allergies to Dasatinib or Quercetin,
  • Hospitalization within 6 months,
  • Unstable coronary artery disease (myocardial infarction within 6 months or angina),
  • Stroke or transient ischemic attack in the past 6 months,
  • Chronic heart failure,
  • Current or chronic history of liver disease,
  • Neurodegenerative disease including Parkinson's disease,
  • Anemia,
  • Chronic renal disease,
  • Drug or alcohol abuse in the last 5 years,
  • QTc prolongation,
  • Thrombocytopenia,
  • Neutropenia,
  • Prolonged prothrombin time or INR,
  • Indications of current fluid retention,
  • History or current diagnosis of pulmonary hypertension,
  • Inability to insonate the middle cerebral artery through a temporal bone window on at least one side using transcranial Doppler ultrasound, or
  • Chronic use of any of the following medications: anti-arrhythmic medications, antipsychotics, anxiolytics, anti-platelet or anti-coagulant medications other than aspirin, quinolone antibiotics, or drugs metabolized by the same liver enzymes as Quercetin or Dasatinib.

Exclusion

    Key Trial Info

    Start Date :

    May 20 2022

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    January 24 2024

    Estimated Enrollment :

    15 Patients enrolled

    Trial Details

    Trial ID

    NCT05422885

    Start Date

    May 20 2022

    End Date

    January 24 2024

    Last Update

    March 17 2025

    Active Locations (1)

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    Hebrew Senior Life

    Boston, Massachusetts, United States, 02131