28 February 2025 - EC approval decision anticipated in second quarter of 2025.
Krystal Biotech today welcomed the EMA's announcement that its CHMP has issued a positive recommendation for the European Commission to approve Vyjuvek (beremagene geperpavec-svdt) for the treatment of wounds in patients with dystrophic epidermolysis bullosa who have mutations in the collagen type VII alpha 1 chain gene, starting from birth.