EC approves Vyvgart for the treatment of gMG

11 August 2022

Belgo-Dutch autoimmune diseases specialist argenx (Nasdaq: ARGX) has announced that the European Commission (EC) has approved Vyvgart (efgartigimod alfa-fcab) as an add-on to standard therapy for adults with generalized myasthenia gravis (gMG) who are anti-acetylcholine receptor (AChR) antibody positive.

The approval is applicable to all European Union (EU) member states plus Iceland, Norway and Liechtenstein. Following the news, shares of argenx rose by 2% to 365.50 euros.

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