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Eisai and Biogen Present Two-Year Study on LEQEMBI® at Alzheimer's Conference

WHAT'S THE STORY?

What's Happening?

Eisai Co., Ltd. and Biogen Inc. have presented findings from a two-year real-world study of lecanemab, marketed as LEQEMBI®, at the Alzheimer's Association International Conference 2025. The study, conducted across 15 U.S. medical centers, focuses on the treatment of early Alzheimer's disease using lecanemab, an anti-Aβ protofibril antibody. The interim report includes data from 178 patients, with 87.4% continuing treatment. The study highlights the drug's impact on maintaining or improving clinical stages in patients, with 83.6% showing stability or improvement. Adverse events were minimal, with ARIA observed in 12.9% of patients, mostly asymptomatic. The study also explores the influence of APOE4 genetic status on treatment outcomes and the growing use of blood-based biomarkers for diagnosis.
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Why It's Important?

The study's findings are significant for the Alzheimer's treatment landscape, offering insights into the real-world application of lecanemab. With Alzheimer's disease affecting millions, the ability to stabilize or improve cognitive function in patients is crucial. The data supports lecanemab's efficacy and safety, potentially influencing treatment protocols and patient care strategies. The study also underscores the importance of genetic factors, such as APOE4 status, in treatment outcomes, which could lead to more personalized approaches in Alzheimer's care. The use of blood-based biomarkers for diagnosis represents a shift towards more accessible and efficient diagnostic methods, potentially improving early detection and treatment initiation.

What's Next?

The final report of the study is expected by late in the third quarter of Eisai's fiscal year ending March 31, 2026. Continued analysis of the data may lead to adjustments in treatment guidelines and further exploration of lecanemab's long-term effects. Eisai and Biogen's collaboration will likely focus on expanding the use of lecanemab globally, with ongoing regulatory reviews in multiple countries. The study's findings may also prompt further research into the role of genetic markers in Alzheimer's treatment, potentially leading to new therapeutic strategies.

Beyond the Headlines

The study highlights ethical considerations in Alzheimer's treatment, such as the balance between drug efficacy and potential adverse effects. The use of real-world data provides a comprehensive view of treatment impacts, but also raises questions about data consistency and biases. The growing reliance on genetic and biomarker data for treatment decisions may lead to discussions on privacy and consent in medical research. Additionally, the collaboration between Eisai and Biogen reflects broader trends in pharmaceutical partnerships aimed at addressing complex diseases like Alzheimer's.

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