KB105 was well tolerated with no adverse events or immune response following redosing Clearly detectable TGM-1 expression in all treated areas following initial and repeat administration. KB105-expressed TGM1 was correctly localized in the epidermis, co-localizing with loricrin, and was

KB105 interim Phase 1/2 clinical data for treatment of autosomal recessive congenital ichthyosis (ARCI) to be announced at the Society for Investigative Dermatology (SID) Annual Meeting in May 2020 B-VEC Phase 3 pivotal study anticipated to start in 1H 2020 B-VEC Phase 1/2 clinical data and

Phase 3 trial of B-VEC (Beremagene Geperpavec, previously “KB103”) to treat dystrophic epidermolysis bullosa (“DEB”) to start in 1H 2020 Interim results on Phase 1/2 clinical study on KB105 to be announced in 1H 2020 Planned filing of two Investigational New Drug Applications (“INDs”), one for rare

PITTSBURGH , Feb. 25, 2020 (GLOBE NEWSWIRE) -- Krystal Biotech, Inc. , (“Krystal”) (NASDAQ: KRYS), a gene therapy company dedicated to developing and commercializing novel treatments for patients suffering from skin diseases, today announced the appointment of Kathryn Romano as chief accounting

PITTSBURGH , Feb. 21, 2020 (GLOBE NEWSWIRE) -- Krystal Biotech Inc. , (“Krystal”) (NASDAQ: KRYS), a gene therapy company dedicated to developing and commercializing novel treatments for patients suffering from skin diseases, today announced that Krish S.

PITTSBURGH , Jan. 24, 2020 (GLOBE NEWSWIRE) -- Krystal Biotech , Inc. (Nasdaq:KRYS), a gene therapy company developing medicines to treat rare diseases, announced today the ground breaking of the second commercial gene therapy facility in Findlay Township, Pennsylvania .

PITTSBURGH , Jan. 21, 2020 (GLOBE NEWSWIRE) -- Krystal Biotech , Inc. (Nasdaq:KRYS), a gene therapy company developing medicines to treat rare diseases, today announced the appointment of Jennifer Chien to the newly created position of chief commercial officer, effective January 20, 2020. Ms.

PITTSBURGH , Nov. 26, 2019 (GLOBE NEWSWIRE) -- Krystal Biotech Inc. , (“Krystal”) (NASDAQ: KRYS), a gene therapy company dedicated to developing and commercializing novel treatments for patients suffering from skin diseases, today announced that Krish S.

Alignment With FDA on GMP Commercial Manufacturing Process for KB103 (Bercolagene telserpavec, “B-VEC”) KB105 Granted Fast Track Designation by the FDA Platform Patent for Delivering any Effector to the Skin Granted by USPTO PITTSBURGH , Nov. 04, 2019 (GLOBE NEWSWIRE) -- Krystal Biotech Inc.

Safety data from all patients (Phase 1 and Phase 2) show that B-VEC was well tolerated with no related adverse events reported. Nine out of 10 of the wounds closed completely (100% closure) following initial administrations of B-VEC. The average time to wound closure was 17.4 days.