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Leqembi® Iqlik™ PDUFA date updated to August 24 in the U.S.
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Therapeutic Goods Administration decides not to register lecanemab in Australia
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FDA accepts filing of Leqembi® (lecanemab-irmb) sBLA for IV maintenance dosing for the treatment of early Alzheimer's Disease
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BioArctic: New lecanemab-data presented at the AD/PD™ 2023 conference
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BioArctic's partner Eisai presents results of lecanemab Phase 3 confirmatory Clarity AD study for Early Alzheimer's disease at CTAD conference
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Eisai initiates rolling submission for the US FDA Biologics license application of lecanemab for early Alzheimer's disease under the accelerated approval pathway
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