
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
Generic 'chemotherapy' label without a specific agent identified. Indicates a cytotoxic regimen used as comparator or backbone.
Taxane chemotherapy that stabilizes microtubules and arrests mitosis. Used in breast, prostate, NSCLC, head and neck, and gastric cancers.
Catalyst Calendar
“A Phase 1/2, Multicenter, Double-Masked, Placebo-Controlled Study of KB801 in Subjects With Stage 2 or 3 Neurotrophic Keratitis — primary completion 2026-12”
“A Double-Blind Crossover of KB803 and Matched Placebo for the Treatment and Prevention of Corneal Abrasions in Dystrophic Epidermolysis Bullosa — primary completion 2026-12”
“KB707-02: A Phase 1/2 Study of Inhaled KB707 in Patients With Advanced Solid Tumor Malignancies Affecting the Lungs — primary completion 2027-02”
“A Phase 1/2, Open-Label, Multi-Center, Dose Escalation and Expansion Study of KB707 in Subjects With Locally Advanced or Metastatic Solid Tumor Malignancies — primary completion 2027-07”
“the Company announced in the press release that it would host a conference call and webcast at 8:30 a.m. ET on July 9, 2025, to discuss neurotrophic keratitis, the Company's KB801 program, and the clinical study design”
“positive safety and efficacy results for the Phase 1 study of KB304 for the treatment of moderate to severe wrinkles of the décolleté”
“the Company announced in the press release that it would host a conference call and webcast at 4:30 p.m. ET on July 24, 2025, to discuss the results of the study, the KB304 clinical development program”