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argenx SE (1AE.F)

Frankfurt - Frankfurt Delayed price. Currency in EUR
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343.10-4.60 (-1.32%)
At close: 08:16AM CEST
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Previous close347.70
Open343.10
Bid341.60 x 0
Ask351.90 x 0
Day's range343.10 - 343.10
52-week range278.90 - 490.50
Volume2
Avg. volume4
Market cap20.759B
Beta (5Y monthly)0.35
PE ratio (TTM)N/A
EPS (TTM)-4.80
Earnings dateN/A
Forward dividend & yieldN/A (N/A)
Ex-dividend dateN/A
1y target estN/A
  • GlobeNewswire

    argenx Data Highlight Evidence that VYVGART and VYVGART Hytrulo Drive Transformative Outcomes for Patients with Debilitating Autoimmune Disease

    ADHERE data show VYVGART® Hytrulo has potential to be first advancement for CIDP patients in 30 years Real-world data demonstrate gMG patients able to significantly reduce steroid use over first six months of initiating VYVGART® treatment April 16, 2024 – 7:00am CET Amsterdam, the Netherlands – argenx SE (Euronext & Nasdaq: ARGX), a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases, today announced that data from its Phase 3 ADHERE tri

  • Insider Monkey

    Here’s Why argenx SE (ARGX) Pulled Back 23% in Q4

    TimesSquare Capital Management, an equity investment management company, released its “U.S. Mid Cap Growth Strategy” fourth-quarter investor letter. A copy of the same can be downloaded here. In the fourth quarter, the strategy underperformed the Russell Midcap Growth Index and returned 13.66% (gross) and 13.44% (net) while the index return was -14.55%. In addition, please check […]

  • GlobeNewswire

    argenx Advances Clinical Development of Efgartigimod in Primary Sjogren’s Disease

    RHO study supports proof-of-concept in primary Sjogren’s disease Decision informed by favorable safety profile and consistency across efficacy and biomarker measures March 27, 2024, 7:00 AM CET Amsterdam, the Netherlands – argenx SE (Euronext & Nasdaq: ARGX), a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases, today announced its plan to continue the development of efgartigimod to Phase 3 in adults with primary Sjogren’s disease (SjD)