FDA approves first topical gene therapy for treatment of wounds in patients with dystrophic epidermolysis bullosa

FDA

19 May 2023 - Today, the US FDA approved Vyjuvek, a herpes-simplex virus type 1 vector-based gene therapy, for the treatment of wounds in patients 6 months of age and older with dystrophic epidermolysis bullosa with mutation(s) in the collagen type VII alpha 1 chain (COL7A1) gene.

Vyjuvek is a genetically modified (engineered in a laboratory) herpes-simplex virus used to deliver normal copies of the COL7A1 gene to the wounds.

Read FDA press release

Michael Wonder

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Michael Wonder

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Outcome , US , Gene therapy