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 15 maio 2024
Gate Neurosciences opens lab in NorthShore Evanston Hospital
Articles about Otsuka Pharmaceutical Co., Ltd.
FDA
Japan's Otsuka Pharma gets FDA approval for Alzheimer's agitation
Allison Rosenthal on LinkedIn: So proud and humbled to announce a
News - Lundbeck
Julie Moore on LinkedIn: We work for the patients but also the
FDA advisers back Lundbeck and Otsuka's Rexulti in Alzheimer's
FDA Accepts sNDA for Rexulti for Alzheimer's Agitation
Christina McGahan posted on LinkedIn
Chip Meyer, Ph.D. on LinkedIn: I'm happy to share that I'm
Mrinalini Sinha on LinkedIn: Otsuka and Lundbeck Issue Statement
Craig Chepke, MD, DFAPA on LinkedIn: Otsuka and Lundbeck Announce
The Alzheimer's drug lecanemab wins full FDA approval. It's a very
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