348,00 €
1,27 % heute
L&S, 26. April, 07:39 Uhr
ISIN
US04016X1019
Symbol
ARGX
Berichte
Sektor
Industrie

argenx SE ADR Aktie News

Neutral
GlobeNewsWire
10 Tage alt
ADHERE data show VYVGART ® Hytrulo has potential to be first advancement for CIDP patients in 30 years
Neutral
GlobeNewsWire
30 Tage alt
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 pla...
Neutral
GlobeNewsWire
etwa ein Monat alt
March 26, 2024 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 the Annual General Meeting of shareholders will be held at 13:00 CET on Tuesday, May 7, 2024 at the Hilton Amsterdam Schiphol at Schiphol Boulevard 701, 1118 BN Schiphol, the Nether...
Neutral
GlobeNewsWire
etwa ein Monat alt
VYVGART ® now approved in Japan for both generalized myasthenia gravis and primary immune thrombocytopenia (ITP)
Negativ
Investors Business Daily
etwa ein Monat alt
Biotech stocks Argenx and Immunovant surged Thursday — and Tourmaline fell — on a rival's lackluster muscle disease drug study.
Neutral
GlobeNewsWire
etwa 2 Monate alt
ADHERE data presentation will highlight first potential innovation for CIDP patients in 30 years Abstracts reflect real-world value and consistent efficacy and safety profile associated with long-term use of VYVGART® and VYVGART® Hytrulo in gMG patients March 7, 2024, 10:01 pm CET Amsterdam, the Netherlands   – argenx SE (Euronext & Nasdaq: ARGX), a global immunology company committed to improv...
Neutral
Seeking Alpha
etwa 2 Monate alt
argenx SE (ARGX) Q4 2023 Earnings Call Transcript
Neutral
GlobeNewsWire
etwa 2 Monate alt
$374 million in fourth quarter and $1.2 billion in full year global net product sales sBLA for VYVGART® Hytrulo for CIDP accepted for priority review by FDA with PDUFA target action date of June 21, 2024 On track to report data from six Phase 2 proof-of-concept trials by end of 2024 Management to host conference call today at 2:30 pm CET (8:30 am ET) February 29, 2024, 7:00 am CET Amsterdam, th...
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