$818.63
11.83%
Nasdaq, Oct 08, 04:05 pm EDT. Closed.
Why the stock moved Why the stock moved Beta
ISIN
US04016X1019
Symbol
ARGX

argenx SE ADR Stock News

Negative
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Proactive Investors
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about 21 hours ago
Shares in argenx SE (NASDAQ:ARGX) fell nearly 15% in New York on Thursday after it discontinued a late-stage trial of its drug Vyvgart in Sjögren's disease. Sjögren's disease is a chronic autoimmune condition characterized by immune-mediated destruction of the glands that produce tears and saliva, causing symptoms including dry eyes and mouth.
Negative
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Investors Business Daily
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about 23 hours ago
Argenx unexpectedly scrapped a study of its drug, Vyvgart, in patients with Sjogren's disease on Thursday. The stock plummeted in response.
Negative
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Reuters
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one day ago
Argenx said on Thursday it had discontinued a late-stage study of its efgartigimod ​drug in adults with Sjögren's disease, ‌an autoimmune condition that damages the glands producing tears and saliva, putting its shares on track ​for their biggest one-day fall in ​almost three years.
Negative
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WSJ
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one day ago
The stock was down 18%, wiping out year-to-date gains after the biotech stopped a late-stage clinical trial of its Vyvgart drug due to lack of efficacy.
Neutral
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GlobeNewsWire
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one day ago
Study met primary endpoint of change from baseline in the ratio of Vh:Cd (p= 0.0176 ) First Phase 2 evidence that blocking CD122 can prevent gluten-induced intestinal damage in people living with celiac disease argenx plans to advance FB102 into Phase 3 development October 8, 2026, 7:00 AM CET    Amsterdam, the Netherlands – argenx SE (Euronext & Nasdaq: ARGX), a global immunology innovation co...
Neutral
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GlobeNewsWire
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one day ago
October 8, 2026, 7:00 AM CET Amsterdam, the Netherlands – argenx SE (Euronext & Nasdaq: ARGX), a global immunology innovation company, today announced that it will discontinue the Phase 3 UNITY study of efgartigimod subcutaneous (SC) (efgartigimod alfa and hyaluronidase-qvfc) in adults with moderate-to-severe Sjögren's disease. The decision is based on the recommendation from an Independent Dat...
Neutral
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GlobeNewsWire
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10 days ago
New data show deepening improvement in ocular MG and sustained one-year efficacy in anti-AChR antibody-negative MG – broadening VYVGART's potential to treat all MG patients Real-world evidence from more than 1,100 U.S. MG patients indicates the value of treating earlier with VYVGART Long-term data reinforce VYVGART's consistent safety and efficacy profile in CIDP, and Phase 4 switch data suppor...
Neutral
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Business Wire
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10 days ago
BOSTON--(BUSINESS WIRE)--Ginkgo Datapoints and Apheris welcome AbbVie, argenx, Lundbeck, and Takeda as Founding Members of the Antibody Developability Consortium.

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