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FDA Approves First Non-Antipsychotic Drug to Treat Agitation Associated with Dementia | FDA

The U.S. Food and Drug Administration today approved an expanded use for Auvelity (dextromethorphan hydrobromide and bupropion hydrochloride) extended-release tablets to treat agitation associated with dementia due to Alzheimer’s disease in adults.

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Axsome: FDA Approves AUVELITY For Treatment Of Agitation Associated With Dementia Due To Alzheimer's | 01.05.26 | finanzen.ch

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FDA approves leucovorin to treat rare cerebral folate deficiency - UPI.com

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https://www.finanzen.at/nachrichten/aktien/axsome-fda-approves-auvelity-for-treatment-of-agitation-associated-with-dementia-due-to-alzheimers-1036093442

Axsome: FDA Approves AUVELITY For Treatment Of Agitation Associated With Dementia Due To Alzheimer's | 01.05.26 | finanzen.at

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FDA Approves First Treatment For Patients With Cerebral Folate Transport Deficiency

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Incyte : FDA Approves Jakafi XR In Myelofibrosis, Polycythemia Vera, And Graft-Versus-Host Disease | 02.05.26 | finanzen.ch

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https://www.fda.gov/news-events/press-announcements/fda-approves-first-ever-gene-therapy-treatment-genetic-hearing-loss-under-national-priority-voucher

FDA Approves First-Ever Gene Therapy for Treatment of Genetic Hearing Loss Under National Priority Voucher Program | FDA

https://www.fda.gov/news-events/press-announcements/fda-approves-first-ever-gene-therapy-treatment-genetic-hearing-loss-under-national-priority-voucher