Last month, Belgo-Dutch autoimmune diseases specialist argenx (Nasdaq: ARGX) announced the European Commission (EC) approval of Vyvgart (efgartigimod alfa-fcab) as an add-on to standard therapy for adults with generalized myasthenia gravis (gMG) who are anti-acetylcholine receptor (AChR) antibody positive.
This is the third major market in which Vyvgart has been approved to treat gMG, following on from approvals in Japan and the USA, and regulatory filings are either under review or planned in a number of other geographies.
Far from looking to big pharma for help, argenx is building its own global commercialization infrastructure in North America, the European Union, the Middle East and Africa region, and in Japan.
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