Does the fully automated Lumipulse plasma p-tau217 immunoassay accurately detect Alzheimer disease pathology in symptomatic patients across diverse clinical settings using predefined biomarker cutoffs?
Can plasma p-tau217 serve as a reliable endpoint for Alzheimer disease clinical trials?
p-tau217 Endpoint
Evaluating plasma p-tau217 as an endpoint for Alzheimer disease clinical trials
Bottom Line: Plasma p-tau217 strongly correlates with amyloid PET and CSF biomarkers, tracks treatment response, and could reduce trial sample sizes by up to 50%.