Epidemiology and Biomarker Study in Alzheimer's Disease

Eli Lilly and Company

Source: ClinicalTrials.gov (U.S. National Library of Medicine), data processed 2026-10-29T09:00:05; modifications: selected fields only; whitespace normalized; brief summary truncated to 2,000 characters. Not a U.S. Government endorsement.

Brief summary

Study AACU determines rates of cognitive worsening in participants within elevated and not elevated plasma P-tau217 cohorts. Participation in AACU will last approximately 7 years.

Source: ClinicalTrials.gov (U.S. National Library of Medicine), data processed 2026-10-29T09:00:05; modifications: selected fields only; whitespace normalized; brief summary truncated to 2,000 characters. Not a U.S. Government endorsement.

Trial details

acronym
ANCHOR-AD
status
RECRUITING
phase
PHASE3
study type
INTERVENTIONAL
enrollment
3400
sponsor
Eli Lilly and Company
conditions
Alzheimer Disease
interventions
OTHER: P-tau217 Test
start date
2025-08-25
start date type
ACTUAL
primary completion date
2033-07-01
has results
false
data source
ClinicalTrials.gov
data processed
2026-10-29T09:00:05
modifications
selected fields only; whitespace normalized; brief summary truncated to 2,000 characters

Record

Archive ID
nct:NCT07142954
Published
Aug 27, 2025
Updated
Jul 7, 2026
Venue
ClinicalTrials.gov
ClinicalTrials.gov
NCT07142954
Categories
Alzheimer Disease
License
ClinicalTrials.gov terms (attribution, processing date, modifications noted)
Provenance
clinicaltrials

Topics