Category: Approval/Launch Region: North America · United States Company: Krystal Biotech Inc

Krystal Biotech seeks US FDA approval for B-VEC to treat patients with dystrophic epidermolysis bullosa

Krystal Biotech seeks US FDA approval for B-VEC to treat patients with dystrophic epidermolysis bullosa
Krystal Biotech, Inc., the leader in redosable gene therapy, announced the submission of a Biologics License Application (BLA) to the US Food and Drug Administration (FDA) seeking approval of B-VEC (beremagene geperpavec) for the treatment of patients with dystrophic epidermolysis bullosa (DEB). B-VEC is an investigational non-invasive, topical gene therapy designed to treat DEB at the molecular level by providing the patient

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