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Home » FDA approves Argenx's Vyvgart for rare autoimmune disease CIDP
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FDA approves Argenx's Vyvgart for rare autoimmune disease CIDP

June 24, 2024
By Randy Osborne
Argenx SE gained U.S. FDA approval of subcutaneously given Vyvgart Hytrulo (efgartigimod alfa and hyaluronidase-qvfc) for adult patients with chronic inflammatory demyelinating polyneuropathy (CIDP). The company’s stock (NASDAQ:ARGX) was up 11.7% to $440.59 at the close of trading June 24. About 24,000 people in the U.S. are being treated for CIDP, and patients are generally diagnosed between 40 and 60 years of age.
BioWorld Regulatory Immune Neurology/psychiatric U.S. Accelerated review FDA

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