UK approval for SC Vyvgart

7 February 2024

The UK's Medicines and Healthcare Regulatory Agency (MHRA) has licensed subcutaneous (SC) injectable Vyvgart (efgartigimod alfa) as an add-on to standard therapy for the treatment of generalised myasthenia gravis (gMG) in adults who are anti-acetylcholine receptor (AChR) antibody positive.

This follows the UK approval of the intravenous (IV) formulation of Vyvgart - from Dutch autoimmune diseases specialist argenx (Euronext & Nasdaq: ARGX) - granted in March 2023.

"SC efgartigimod provides a new and easier-to-administer treatment option for these people, with the ability to potentially impact their quality of life and disease burden"

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