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FDA Accepts Eisai s Filing of LEQEMBI® (lecanemab-irmb) Supplemental Biologics License Application for IV Maintenance Dosing for the Treatment of Early Alzheimer s Disease

FDA Accepts Eisai s Filing of LEQEMBI® (lecanemab-irmb) Supplemental Biologics License Application for IV Maintenance Dosing for the Treatment of Early Alzheimer s Disease
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FDA Accepts Eisai s Filing of LEQEMBI® (lecanemab-irmb)

FDA Accepts Eisai s Filing of LEQEMBI® (lecanemab-irmb)
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Biogen Inc : FDA Accepts Eisai s Filing of LEQEMBI® (lecanemab-irmb) Supplemental Biologics License Application for IV Maintenance Dosing for the Treatment of Early Alzheimer s Disease

TOKYO and CAMBRIDGE, Mass., June 09, 2024 (GLOBE NEWSWIRE) Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts

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FDA Accepts Eisai s Filing of LEQEMBI (lecanemab-irmb) Supplemental Biologics License Application for IV Maintenance Dosing for the Treatment of Early Alzheimer s Disease

FDA Accepts Eisai s Filing of LEQEMBI (lecanemab-irmb) Supplemental Biologics License Application for IV Maintenance Dosing for the Treatment of Early Alzheimer s Disease
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Depression, antidepressants, epigenetic age acceleration, and mortality in postmenopausal women

A new research paper titled "Relationships of depression and antidepressant use with epigenetic age acceleration and all-cause mortality among postmenopausal women" has been published in Aging.

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