Krystal Biotech Announces FDA Approval of Updated VYJUVEK® Label

Provided By GlobeNewswire

Last update: Sep 15, 2025

Revised label allows treatment of DEB patients from birth

VYJUVEK can now be applied by patients and caregivers

PITTSBURGH, Sept. 15, 2025 (GLOBE NEWSWIRE) -- Krystal Biotech, Inc. (the “Company”) (NASDAQ: KRYS) announced today that the United States Food and Drug Administration (FDA) approved a label update for VYJUVEK^® (beremagene geperpavec-svdt) that expands the VYJUVEK eligible patient population to include dystrophic epidermolysis bullosa (DEB) patients from birth and provides patients full flexibility with respect to VYJUVEK application and managing wound dressings.