US FDA approves syringe version of Argenx's immune disorder drug
ReutersApr 10, 2025 9:51 PM
April 10 (Reuters) - The U.S. Food and Drug Administration has approved a pre-filled syringe version of Netherlands-based Argenx SE's ARGX.BR blockbuster immune disorder drug, Vyvgart, giving patients the more convenient option of at-home self administration, the company said on Thursday.
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