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argenx SE (0QW0.IL)

IOB - IOB Delayed price. Currency in EUR
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351.45+4.20 (+1.21%)
At close: 06:13PM BST
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Previous close347.25
Open346.00
Bid333.90 x N/A
Ask366.70 x N/A
Day's range342.50 - 351.34
52-week range272.40 - 494.00
Volume7,012
Avg. volume30,990
Market cap20.676B
Beta (5Y monthly)0.53
PE ratio (TTM)N/A
EPS (TTM)-6.55
Earnings dateN/A
Forward dividend & yieldN/A (N/A)
Ex-dividend dateN/A
1y target estN/A
  • Globe Newswire

    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)