Key Takeaways Vyjuvek is now approved for DEB patients from birth, with self-administration at home allowed.Vyjuvek posted $184.2M in 1H25 sales, with growth expected from the U.S., EU, and Japan labels.KRYS prioritizes oncology candidate KB707, with an FDA end-of-phase II meeting set for October.Krystal Biotech, Inc.’s (KRYS) lead drug Vyjuvek is a non-invasive, topical, redosable gene therapy approved in the United States, Europe, and Japan for the treatment of dystrophic epidermolysis bullosa (DEB).Kryst ...