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argenx SE/$ARGX

1D1W1M3M6MYTD1Y5YMAX

About argenx SE

Argenx is a Dutch biopharmaceutical company focused on developing antibody-based therapies for rare autoimmune diseases. The company's lead product, Vyvgart (efgartigimod), was approved by the FDA in December 2021 for the treatment of generalized myasthenia gravis (gMG). In 2022, Argenx also received FDA approval for Vyvgart Hytrulo, a subcutaneous formulation of Vyvgart, offering a more convenient option compared with Vyvgart's intravenous administration. In 2024, the FDA approved Vyvgart Hytrulo for Chronic Inflammatory Demyelinating Polyneuropathy, a rare immune-mediated neuromuscular disorder of the peripheral nervous system. Argenx is focused on innovation and developing its pipeline for treatments such as primary immune thrombocytopenia, thyroid eye disease, and Sjogren's Disease.
Ticker
$ARGX
Sector
Health
Primary listing
NASDAQ
Employees
1,863
Website
argenx.com

argenx SE Metrics

BasicAdvanced
$55B
30.26
$28.88
-0.04
-

What the Analysts think about argenx SE

Analyst ratings (Buy, Hold, Sell) for argenx SE stock.
Analyst projections of the future price of argenx SE stock.

Bulls say / Bears say

VYVGART product sales reached $1.5 billion in the second quarter, up 60% year on year and 17% from the previous quarter. That pace of growth supports the case that argenx is turning its lead medicine into a substantial commercial business. (argenx)
The FDA expanded VYVGART’s gMG label to cover all adult serotypes, including patients who test negative for AChR antibodies. This broadens the group of patients the company can target in its largest market. (argenx)
A Phase 3 study of VYVGART Hytrulo in autoimmune myositis met its primary endpoint, with a statistically significant and clinically meaningful improvement versus placebo. If the results support approval, myositis could add another use for the established drug franchise. (argenx)
Argenx stopped its Phase 3 Sjögren’s study after an interim review found it was unlikely to meet its primary endpoint. The failure removes a potential growth opportunity and highlights the risk in extending VYVGART into new diseases. (The Wall Street Journal)
The company spent $929 million on research and development in the first half of 2026, up from $600 million a year earlier. Such rising investment increases the pressure on its pipeline to deliver successful products and indications. (SEC)
The business remains heavily reliant on VYVGART: the company reported $2.8 billion in VYVGART sales in the first half, equal to its total product net sales. Any slowdown in uptake or loss of market share would therefore have a direct effect on the overall business. (SEC)
Data summarised monthly by Lightyear AI. Last updated on 8 Oct 2026.

argenx SE Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

argenx SE Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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