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The medication received marketing authorization in the European Union through the Decentralized Procedure in the third quarter of 2022

Lidbury PS, Korbut R, Vane JR

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While further studies are needed to assess longterm safety, dosing, and clinical relevance, the work points to a promising intranasal drugdelivery platform that emphasizes stability, retention, and neuroprotectionkey considerations for managing a chronic neurodegenerative disease