argenx SE (ARGX) CEO Tim Van Hauwermeiren on Q4 2020 Results - Earnings Call Transcript
- Biologics License Application (BLA) for IV efgartigimod accepted for review by U.S. Food and Drug Administration (FDA) for generalized myasthenia gravis (gMG)
February 25, 2021 Breda, the Netherlands – argenx (Euronext & Nasdaq: ARGX), a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases and canc

argenx announces closing of global offering

04:01pm, Friday, 05'th Feb 2021
Regulated information
Regulated information — Inside information
Regulated information — Inside information

argenx Issues Statement Concerning Efgartigimod

09:37am, Tuesday, 02'nd Feb 2021
-No observed elevation of cholesterol markers related to treatment with efgartigimod
Regulated information — Inside information
Gracell Biotech completed a $209 million NASDAQ IPO for its next-gen CAR-T treatments. Zai Lab acquired greater China rights to an argenx SE novel treatment for autoimmune indications in a deal worth
Breda, the Netherlands – Jan. 8, 2021 – argenx (Euronext & Nasdaq: ARGX), a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases and cance
January 4, 2021 Breda, the Netherlands / Ghent, Belgium – argenx (Euronext & Nasdaq: ARGX), a global immunology company committed to improving the lives of people suffering from severe autoimmune di
November 23, 2020 Breda, the Netherlands / Ghent, Belgium – argenx (Euronext & Nasdaq: ARGX), a global immunology company committed to improving the lives of people suffering from severe autoimmune
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