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Krystal Biotech Announces United Kingdom MHRA Approval of VYJUVEK® for the Treatment of Dystrophic Epidermolysis Bullosa

VYJUVEK approved for the treatment of DEB from birth with flexible administration options similar to those already granted in the United States, European Union, and Japan VYJUVEK is the first genetic medicine approved in the United Kingdom for the treatment of DEB PITTSBURGH, May 18, 2026 (GLOBE NEWSWIRE) -- Krystal Biotech, Inc. (the “Company”) (NASDAQ: KRYS) today announced that, on May 15, 2026, the United Kingdom Medicines and Healthcare products Regulatory Agency (MHRA) granted marketing au

articleKrystal Biotech, Inc.May 18, 20264/company/krystal-biotech-inc/news/krystal-biotech-announces-united-kingdom-mhra-approval-of-vyjuvekr-for-the-treatment-of-dystrophic-epidermolysis-bullosa
Krystal Biotech Announces United Kingdom MHRA Approval of VYJUVEK® for the Treatment of Dystrophic Epidermolysis Bullosa

About this update from Krystal Biotech, Inc.

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More updates from Krystal Biotech, Inc.

MHRAUnited Kingdomdystrophic epidermolysis bullosaKrystal Biotechthe Companygenetic medicineEuropean UnionUnited StatesVYJUVEK