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FinancialContent

argenx SE - American Depositary Shares (NQ:ARGX)

913.97 -22.03 (-2.35%)
Delayed Quote Updated: 1:05 PM EDT, Oct 2, 2026 Add to My Watchlist
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Press Releases about argenx SE - American Depositary Shares

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argenx Presents New Data at AANEM and MGFA Scientific Session Showcasing Earlier and Sustained Treatment in MG and CIDP with VYVGART and Progress Across its Neuromuscular Pipeline
From argenx SE
Via GlobeNewswire
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argenx announces results of Extraordinary General Meeting of Shareholders and appointment of Thomas M. Brakel and Khurem Farooq as Non-Executive Directors
From argenx SE
Via GlobeNewswire
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argenx to Present at Upcoming Investor Conferences
From argenx SE
Via GlobeNewswire
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argenx Completes Acquisition of Forte Biosciences, Inc.
From argenx SE
Via GlobeNewswire
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argenx Announces Positive Topline Results from Phase 3 ALKIVIA Trial of Efgartigimod in Autoimmune Myositis
From argenx SE
Via GlobeNewswire
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argenx Announces Commencement of Tender Offer to Acquire Forte Biosciences, Inc.
From argenx SE
Via GlobeNewswire
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argenx announces Extraordinary General Meeting of Shareholders on September 17, 2026
From argenx SE
Via GlobeNewswire
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argenx to Acquire Forte Biosciences, Inc., Adding First-in-Class Anti-CD122 Antibody, FB102, to Its Immunology Pipeline
From Forte Biosciences, Inc.
Via Business Wire
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argenx to Acquire Forte Biosciences, Inc., Adding First-in-Class anti-CD122 Antibody, FB102, to its Immunology Pipeline
From argenx SE
Via GlobeNewswire
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argenx Reports Half Year 2026 Financial Results and Provides Second Quarter Business Update
From argenx SE
Via GlobeNewswire
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argenx to Report Half Year 2026 Financial Results and Second Quarter Business Update on July 23, 2026
From argenx SE
Via GlobeNewswire
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argenx to Host Autoimmune Myositis R&D Webinar
From argenx SE
Via GlobeNewswire
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argenx Presents New Efgartigimod Data Showing Long-Term Sustained Patient Benefit in Myositis and Sjogren’s Disease at EULAR 2026
From argenx SE
Via GlobeNewswire
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argenx to Host Myositis R&D Webinar on June 23, 2026
From argenx SE
Via GlobeNewswire
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argenx to Present at Upcoming Investor Conferences
From argenx SE
Via GlobeNewswire
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argenx Announces U.S. FDA Approval Expanding VYVGART and VYVGART Hytrulo for Use in All Adult Patients Living with gMG
From argenx SE
Via GlobeNewswire
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argenx Reports First Quarter 2026 Financial Results and Provides Business Update
From argenx SE
Via GlobeNewswire
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argenx to Present at BofA Securities 2026 Health Care Conference
From argenx SE
Via GlobeNewswire
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argenx Announces Results of Annual General Meeting and Board of Directors’ Appointment of Karen Massey as Chief Executive Officer
From argenx SE
Via GlobeNewswire
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argenx to Report First Quarter 2026 Financial Results and Business Update on May 7, 2026
From argenx SE
Via GlobeNewswire
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argenx Brings Neuromuscular Leadership to AAN 2026 with New Data Supporting Broader VYVGART Use Across MG and CIDP
From argenx SE
Via GlobeNewswire
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argenx announces Annual General Meeting of Shareholders on May 6, 2026
From argenx SE
Via GlobeNewswire
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argenx to Present New Data at 2026 AAN Annual Meeting that Continue to Transform Patient Outcomes in MG and CIDP and Build Upon Strength of Pipeline
From argenx SE
Via GlobeNewswire
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argenx Reports Full Year 2025 Financial Results and Provides Fourth Quarter Business Update
From argenx SE
Via GlobeNewswire
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argenx Announces Positive Topline Results from Phase 3 ADAPT OCULUS Trial of VYVGART in Ocular Myasthenia Gravis
From argenx SE
Via GlobeNewswire
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argenx to Present at TD Cowen 46th Annual Healthcare Conference
From argenx SE
Via GlobeNewswire
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argenx to Report Full Year 2025 Financial Results and Fourth Quarter Business Update on February 26, 2026
From argenx SE
Via GlobeNewswire
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argenx Announces FDA Acceptance of Supplemental Biologics License Application with Priority Review for VYVGART in AChR-Ab Seronegative gMG
From argenx SE
Via GlobeNewswire
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argenx Highlights 2026 Strategic Priorities
From argenx SE
Via GlobeNewswire
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argenx to Present at 44th Annual J.P. Morgan Healthcare Conference
From argenx SE
Via GlobeNewswire
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