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argenx Announces FDA Acceptance of Supplemental Biologics License Application with Priority Review for VYVGART Hytrulo in Chronic Inflammatory Demyelinating Polyneuropathy
argenx SE - American Depositary Shares (ARGX)
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Source: GlobeNewswire
US:NASDAQ Investor Relations: investor.argenx.com/phoenix.zhtml?c=254223&p=irol-presentations
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Prescription Drug User Fee Act (PDUFA) target action date is June 21, 2024 If approved, VYVGART® Hytrulo will be the first neonatal Fc receptor (FcRn) blocker to trea
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