A Donanemab (LY3002813) Study in Participants With Preclinical Alzheimer's Disease (TRAILBLAZER-ALZ 3)

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

The main purpose of this study is to evaluate the safety and efficacy of donanemab in participants with preclinical Alzheimer's Disease (AD) over up to 332 weeks. Approximately 800 additional participants will be enrolled in the 12-month Addendum 7 to assess safety of a different titration regimen.

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

status
ACTIVE_NOT_RECRUITING
phase
PHASE3
study type
INTERVENTIONAL
enrollment
2996
sponsor
Eli Lilly and Company
conditions
Alzheimer Disease
interventions
DRUG: Donanemab; DRUG: Placebo
start date
2021-08-27
start date type
ACTUAL
primary completion date
2027-11-01
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:NCT05026866
Published
Aug 30, 2021
Updated
Jan 21, 2026
Venue
ClinicalTrials.gov
ClinicalTrials.gov
NCT05026866
Categories
Alzheimer Disease
License
ClinicalTrials.gov terms (attribution, processing date, modifications noted)
Provenance
clinicaltrials

Topics