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Development of a Home Test for Measuring Blood P-tau217 in Alzheimer's Disease Using the Tasso Lancet Device

Recruitingn/aAges 40 Years - 90 YearsAllNeurogen Biomarking LLC
NCT07701161 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This study compares p-tau217 concentrations in blood collected via the Tasso device versus standard venipuncture in subjects with and without Alzheimer's disease, including a subset with confirmed amyloid pathology.

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📋 Eligibility rules (as published)
Inclusion Criteria: * AD Amyloid PET/CSF confirmed, healthy control, or amyloid-negative non-AD cognitive impairment Age 40-90 Able to complete Tasso and venipuncture collection Caregiver consent/assistance available if needed Exclusion Criteria: * Uncontrolled systemic conditions Recent surgery/hospitalization (3 months) Other dementia drug trial (2 months) Pregnancy Prior Donanemab or Lecanemab use
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What it tests

  • Not listed
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Where

5 sites
Insigth Hospital and Medical Center Chicago
Chicago, United States
Insight Hospital and Medical Center Dearborn
Dearborn, United States
Insight Institute of Neurology and Neurosurgery
Flint, United States
Memorial Healthcare Hospital
Owosso, United States
Wake Forest Baptist Medical Center
Winston-Salem, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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