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

NCT07701161 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2026-07-14

No results posted yet for this study

Summary

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.

Conditions

  • Alzheimer s Disease
  • MCI Conversion to Dementia
  • pTau217
  • Biomarkers

Sponsors & Collaborators

  • Neurogen Biomarking LLC

    lead INDUSTRY

Principal Investigators

  • Rany Aburashed · Insight Health Systems

Eligibility

Min Age
40 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-01-13
Primary Completion
2026-03-20
Completion
2026-08-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07701161 on ClinicalTrials.gov