
KRYS
Krystal Biotech develops gene therapies using a proprietary herpes simplex virus (HSV-1) based vector platform, primarily focused on genetic skin diseases. The company's lead product, VYJUVEK, was approved by the FDA in May 2023 and the European Commission in April 2025 for treating dystrophic epidermolysis bullosa (DEB), and it is now in the commercialization stage across the United States, European Union, Japan, and other markets.
Pipeline
Catalyst Calendar
“phase 1 (PEARL-1) positive interim safety and efficacy results for KB301 in the treatment of lateral canthal lines and dynamic wrinkles of the décolleté”
“the Company and Krystal Biotech, Inc. would host a conference call and webcast at 4:30 p.m. ET on August 28, 2024, to discuss the PEARL-1 Cohort 3 and Cohort 4 interim results”