drugset / Trial / NCT04468659

AHEAD 3-45 Study: A Study to Evaluate Efficacy and Safety of Treatment With Lecanemab in Participants With Preclinical Alzheimer's Disease and Elevated Amyloid and Also in Participants With Early Preclinical Alzheimer's Disease and Intermediate Amyloid

NCT04468659

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study is to determine whether treatment with lecanemab is superior to placebo on change from baseline of the Preclinical Alzheimer Cognitive Composite 5 (PACC5) at 216 weeks of treatment (A45 Trial) and to determine whether treatment with lecanemab is superior to placebo in reducing brain amyloid accumulation as measured by amyloid positron emission tomography (PET) at 216 weeks of treatment (A3 Trial). This study will also evaluate the long-term safety and tolerability of lecanemab in participants enrolled in the Extension Phase.

Timeline

Start
2020-07-14
Primary completion
2028-12-21
Completion
2031-01-16

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lecanemab Monoclonal antibody 10 mg/kg Intravenous

Indications