Last reviewed · How we verify

NCT06622135

Home Test for Measuring Plasma P-tau217 in Alzheimer's Disease

Terminated NA Last updated 11 February 2025
What this trial tests

NA trial testing Tasso Lancet Device in Alzheimer Disease in 16 participants. Terminated before completion.

Timeline
19 September 2024
Primary endpoint
7 December 2024
7 December 2024

Quick facts

Lead sponsorInsight Research Institute
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment16
Start date19 September 2024
Primary completion7 December 2024
Estimated completion7 December 2024
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Insight Research Institute

Who can join

Adults 55 to 90, any sex, with Alzheimer Disease or Healthy Subjects. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this is to develop an easy at home test that can be used to assist in diagnosing Alzheimer's disease (AD). The test will use an FDA approved device for at home blood sample collection. The blood samples will be evaluated to determine if the concentration of p-tau217, a biomarker that is elevated in AD patients, measured from blood samples collected using the at home device is comparable to the results obtained from blood samples collected by venipuncture.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Alzheimer Disease

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06622135.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing