argenx reports Q3 2026 results with $1.7bn sales growth
Revenue rose 54% year-over-year to $1.7 billion. The company advances FB102 into Phase 3 for celiac disease and continues pipeline developments across immunology indications.
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Immunology-focused biopharmaceutical company
argenx.comLast updated
In short: argenx posted strong sales growth, acquired Forte Biosciences, reported positive myositis data, and discontinued a Sjögren's study.
Revenue rose 54% year-over-year to $1.7 billion. The company advances FB102 into Phase 3 for celiac disease and continues pipeline developments across immunology indications.
Results show efgartigimod provides clinically meaningful improvements in muscle strength for immune-mediated necrotizing myopathy and dermatomyositis patients compared to placebo.
The drug met its primary endpoint preventing intestinal damage. argenx plans to advance the first-in-class CD122 inhibitor into Phase 3 trials.
The UNITY trial stopped for futility. The IDMC concluded the study could not meet its primary endpoint.
Shots:The US FDA has accepted argenx’s sBLA for Vyvgart (efgartigimod alfa-fcab, IV) & Vyvgart Hytrulo (efgartigimod alfa & hyaluronidase-qvfc, SC) to treat pediatric generalized myasthenia...
Belgian-Dutch pharmaceutical firm argenx said on Thursday that global sales of its leading autoimmune drug Vyvgart rose 54% in the third quarter, as it...
Results from the global Phase 3 ALKIVIA study, the first registrational study investigating an FcRn blocker in autoimmune myositis, show efgartigimod provides clinically meaningful improvements...
Yesterday, argenx's stock slipped by more than 2%—with its shares still down slightly as of Friday morning—after the Dutch pharma...
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