Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA) Approval of Supplemental New Drug Application (sNDA) for REXULTI® (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due to Alzheimer's Disease

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Last updated 12 abril 2025
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Otsuka and Lundbeck Announce REXULTI for Alzheimer's Agitation
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Tim Hunt on LinkedIn: Otsuka and Lundbeck Announce U.S. Food and
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
FDA Accepts sNDA for Rexulti for Alzheimer's Agitation
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Articles about Otsuka Pharmaceutical Co., Ltd.
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Brexpiprazole Gets Priority Review for Agitation With Alzheimer
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
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Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Jennifer Repella-Gordon on LinkedIn: Otsuka and Lundbeck Announce
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
FDA
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Otsuka and Lundbeck Issue Statement on U.S. Food and Drug
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Chip Meyer, Ph.D. on LinkedIn: I'm happy to share that I'm
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
News Releases Otsuka Pharmaceutical Co., Ltd.

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