公司资料

Argenx 股价、新闻与催化剂

股票代码:
ARGX
交易所:
NASDAQ
行业:
Antibody Drugs
所在地:
Ghent, Belgium and listed in the U

股票表现

987.84 USD (+16.04%)

收盘价

最后更新: 2026年8月17日

49.9B USD

市值

股价为何变动

Following the latest company update, “argenx Announces Positive Topline Results from Phase 3 ALKIVIA Trial of Efgartigimod in Autoimmune Myositis”, ARGX closed up 16.0% at $987.84 on Aug 17, 2026. The move occurred in the trading session associated with this clinical readout update.

公司概览

Global Immunology Company

Argenx develops therapies for severe autoimmune diseases. Its core commercial asset, VYVGART/efgartigimod, targets FcRn to reduce circulating IgG autoantibodies and has established a commercial base in generalized myasthenia gravis, chronic inflammatory demyelinating polyneuropathy, and selected regional indications such as primary immune thrombocytopenia.

VYVGART Expansion Strategy

The company is expanding VYVGART into ocular myasthenia gravis, autoimmune myositis, primary immune thrombocytopenia, Sjögren’s disease, and Graves’ disease. VYVGART Hytrulo, the subcutaneous formulation, broadens the franchise through more convenient administration.

Global Commercial Franchise

VYVGART is commercialized across multiple regions and formulations, with the expanded U.S. label covering all adult gMG serotypes. The franchise provides argenx with an established commercial organization that can support additional indications and future immunology assets.

Empasiprubart as a Second Franchise

Empasiprubart, a complement C2-targeting antibody, represents argenx’s second potential pipeline-in-a-product. It is being studied in multifocal motor neuropathy, CIDP, delayed graft function, and combination therapy with VYVGART in gMG.

Earlier Immunology Pipeline

Additional programs include next-generation FcRn candidates ARGX-213 and ARGX-124, MuSK agonist adimanebart, anti-IgA antibody ARGX-121, and other candidates emerging from the company’s Immunology Innovation Program.

Vision 2030 Framework

Argenx’s long-term strategy targets 50,000 patients treated globally, ten labeled indications, and five pipeline candidates in registrational development by 2030. The framework links continued VYVGART expansion with the creation of multiple independent immunology franchises.

未来催化剂

  • Topline data from the registrational ALKIVIA study of VYVGART in autoimmune myositis are expected in the third quarter of 2026.
  • Topline data from the registrational EMPASSION study of empasiprubart in multifocal motor neuropathy are expected in the fourth quarter of 2026.
  • Topline results from the ADVANCE-NEXT study in primary ITP are expected in the first half of 2027, followed by UNITY data in Sjögren’s disease in the second half of 2027.
  • A VYVGART SC autoinjector is expected to launch across all approved indications in 2027.
  • A registrational study of adimanebart in congenital myasthenic syndromes, a Phase 2 study of ARGX-121 in IgA nephropathy, and Phase 1 studies of ARGX-118 and ARGX-125 are planned to advance during 2026.

近期新闻

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