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Argenx Se ADR (NQ: ARGX )

377.75 -1.55 (-0.41%)
Streaming Delayed Price Updated: 11:21 AM EDT, Jun 11, 2024 Add to My Watchlist
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Press Releases about Argenx Se ADR

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argenx Appoints Ana Cespedes to Board of Directors
From argenx SE
Via GlobeNewswire
argenx to Present Pivotal ADVANCE Trial Data During ASH Plenary Session Highlighting VYVGART® (efgartigimod alfa-fcab) as Potential New Treatment Modality for Immune Thrombocytopenia
From argenx SE
Via GlobeNewswire
argenx Enters Into Agreement To Acquire Priority Review Voucher
From argenx SE
Via GlobeNewswire
argenx Announces U.S. FDA Acceptance of Biologics License Application for Subcutaneous Efgartigimod in Generalized Myasthenia Gravis with Priority Review
From argenx SE
Via GlobeNewswire
argenx to Present at Upcoming Investor Conferences
From argenx SE
Via GlobeNewswire
argenx Reports Third Quarter 2022 Financial Results and Provides Business Update
From argenx SE
Via GlobeNewswire
argenx to Report Third Quarter 2022 Financial Results and Business Update on October 27, 2022
From argenx SE
Via GlobeNewswire
argenx announces Extraordinary General Meeting of Shareholders on September 8, 2022
From argenx SE
Via GlobeNewswire
argenx Reports Half Year 2022 Financial Results and Provides Second Quarter Business Update
From argenx SE
Via GlobeNewswire
argenx to Present New Data from Generalized Myasthenia Gravis Program at 2022 American Academy of Neurology Annual Meeting
From argenx SE
Via Business Wire
argenx Announces Positive Topline Phase 3 Data From ADAPT-SC Study Evaluating Subcutaneous Efgartigimod for Generalized Myasthenia Gravis
From argenx SE
Via Business Wire
argenx Announces VYVGART™ Approval in Japan for the Treatment of Generalized Myasthenia Gravis
From argenx
Via Business Wire
argenx Highlights Strategic Priorities for 2022
From argenx
Via Business Wire
argenx Announces U.S. Food and Drug Administration (FDA) Approval of VYVGART™ (efgartigimod alfa-fcab) in Generalized Myasthenia Gravis
From argenx SE
Via Business Wire
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