argenx N.V.'s position as the leading player in the FcRn inhibitor class has been cemented with regulators in the US giving the green light to a more convenient subcutaneous formulation of its big-selling generalized myasthenia gravis (gMG) treatment Vyvgart.
Argenx Gets Under Skin Of Rivals With Vyvgart Hytrulo Approval
Subcutaneous Formulation of Egartigimod Alfa Gets FDA OK
The US approval of a more convenient formulation of its myasthenia gravis therapy, Vyvgart, should cement its market position as well as change the definition of what being "well-controlled means for patients", Argenx hopes.

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The head of the Spanish medical dermatology specialist told Scrip that maintaining the status quo will only result in the continent’s life sciences sector slipping further behind the US and China.
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RemeGen is planning to complete enrolment in the global Phase III RemeMG study with telitacicept in generalized myasthenia gravis by the end of 2025 or early 2026. The Chinese firm has already sidelined two other global Phase III trials with the molecule to prioritize the indication.
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