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Eisai submits sBLA to USFDA for its key drug to treat early Alzheimer's disease - Pharma News

Eisai submits sBLA to USFDA for its key drug to treat early Alzheimer's disease - Pharma News
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Submission of Leqembi® (lecanemab-irmb) sBLA for IV maintenance dosing for the treatment of early Alzheimer's disease to the U.S. FDA completed

Stockholm, Sweden, April 1, 2024 - BioArctic AB s partner Eisai announced today that Eisai has submitted a supplemental Biologics License Application for monthly lecanemab-irmb intravenous . ....

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BioArctic: New data on lecanemab presented at the 2024 AD/PD™ congress

BioArctic: New data on lecanemab presented at the 2024 AD/PD™ congress
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BioArctic: New data on lecanemab presented at the 2024 AD/PDtm congress

BioArctic: New data on lecanemab presented at the 2024 AD/PDtm congress
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BioArctic: Latest data on lecanemab to be presented at the 2024 AD/PD™ congress

BioArctic: Latest data on lecanemab to be presented at the 2024 AD/PD™ congress
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United Kingdom , Great Britain , Miia Kivipelto , Lars Lannfelt , Lynn Kramer , Jeffrey Cummings , Jiang Millington , Oskar Bosson , Robert Perneczky , Ministry Of Health , National Institute On , Drug Administration , Washington University School Of Medicine , International Conference On Alzheimer , Vp Communications , National Institutes Of Health , Alzheimer Clinical Trial Consortium , Alzheimer Network Trials Unit , National Medical Products Administration , Asset In Development , Professor Lars , Professor Lars Lannfelt , Chief Clinical Officer , Targeting Therapies , Director Corporate Communication , Social Media ,