The LEADER study evaluated 432 patients across 13 clinical sites in the United States, tracking treatment outcomes through electronic medical records and clinician assessments. Data revealed that 75.9% of participants remained stable, while 6.6% experienced a measurable improvement in their condition. These results were uniform regardless of a patient's sex, race, ethnicity, or APOE genotype.
Safety profiles remained consistent with the FDA-approved label for the drug. Amyloid-related imaging abnormalities, or ARIA, occurred in 12.3% of the study population, with most cases presenting as asymptomatic or mild. Notably, the incidence of these abnormalities did not increase significantly among patients concurrently using antithrombotic medications. Nearly 87% of the cohort opted to continue their Leqembi regimen, underscoring the long-term persistence observed in real-world practice.
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