Argenx to Host R&D Webinar on Myositis on June 23, 2026
Argenx announced on Thursday the organization of a webinar dedicated to its research and development in myositis, an autoimmune rheumatic disease. This event is part of a series of presentations highlighting the group's project portfolio and its work around its main treatment.
The webinar, scheduled for June 23, 2026, at 2:00 PM Eastern Time, will focus on myositis, an autoimmune condition in the rheumatic field characterized by progressive muscle degradation and a significant clinical burden for patients. Teams from Argenx and clinicians specialized in treating this disease will present advances in understanding the biology of myositis, including the role of autoantibodies as key factors in the pathology.
The event will also address the design of the ALKIVIA clinical program and the clinical and commercial opportunity of efgartigimod, the neonatal Fc receptor (FcRn) blocker developed and marketed by Argenx.
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This webinar represents the second event in the 'mini' series launched by Argenx to highlight its portfolio and research and development strategy. A recording of the presentation will be available on the group's investor relations site for about a year after its broadcast.
SectorPharmacie et biotechnologies›Biotechnologies
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Context
Period
Period: 9M 2026
Key reported figures
Revenue: 4 605 millions de dollars
Quarterly revenue: 4 605 millions de dollars
Revenue growth: 57,4 %
Net income: 1 344 millions de dollars
Guidance from the release
argenx remains on track to achieve its 'Vision 2030' anchored in the ambition to treat 50,000 patients globally
Risks mentioned
The risk that early stage clinical trials may not be predictive of results in later stage or large scale clinical trials
Demand and commercialization risks for argenx's products and product candidates, including new indications
Regulatory and pricing uncertainties for argenx's products and product candidates if approved
Opportunities identified
Vision 2030 targets: treat 50,000 patients globally, secure 10 labeled indications, and progress five pipeline candidates
Multiple label and indication expansions for VYVGART being pursued across additional autoimmune diseases
Next-generation FcRn molecules (ARGX-213 Phase 3-ready, ARGX-124 in Phase 1) advancing through development
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