Argenx (ARGX) announced the Committee for Medicinal Products for Human Use of the European Medicines Agency has recommended European Commission approval of Vyvgart 1000mg for subcutaneous injection as a monotherapy for the treatment of adult patients with progressive or relapsing active chronic inflammatory demyelinating polyneuropathy after prior treatment with corticosteroids or immunoglobulins.
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Read More on ARGX:
- Argenx Se’s Revenue Growth Potential Boosted by Vyvgart Hytrulo’s Market Impact and Increased Treatment Cycles
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- Argenx Se’s Growth Potential Bolstered by Vyvgart Hytrulo Approval and Strategic Positioning
- Vyvgart for self-administration ‘immaterial’ to Option Care, says JPMorgan
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