argenx announces FDA approval for seronegative gMG treatment
The treatment targets a historically underserved community with a rare form of myasthenia gravis.
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Immunology-focused biopharmaceutical company
argenx.comLast updated
In short: argenx achieved its first year of operating profitability and reported record 2025 sales of $4.2 billion, driven by the expansion of its Vyvgart drug.
The treatment targets a historically underserved community with a rare form of myasthenia gravis.
Approval extends indication to all adult gMG serotypes based on Phase 3 ADAPT SERON data.
Advancements in MG and CIDP drive momentum. Upcoming milestones include data readouts in myositis and MMN.
Global product net sales reach $1.3 billion, up 63% year-over-year. Pipeline updates include upcoming PDUFA for seronegative gMG and topline results for several studies.
Efgartigimod. Argenx.
Sanofi discontinues Phase 3 riliprubart study for CIDP due to low efficacy. SNY stock ticks up. Read the market & analyst reaction.
Argenx SE (ARGX), a commercial-stage biopharmaceutical company, announced new clinical data from Phase 2 extension studies for efgartigimod in the treatment of myositis and Sjogren's...
ALKIVIA+ data in myositis indicate efgartigimod provides sustained, clinically meaningful improvements and consistent safety RHO+ data in Sjogren’s disease indicate maintenance of response following ...
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