Verrica Pharmaceuticals Inc., a dermatology therapeutics company, engages in the development and commercialization of medications for the treatment of dermatologic diseases in the United States. The company offers YCANTH (VP-102) a drug-device combination that contains a GMP-controlled formulation of cantharidin for the treatment of molluscum in adult and pediatric patients, as well as for the treatment of common warts. It also develops VP-315, an oncolytic peptide-based injectable therapy that is in phase II clinical trial for the treatment of dermatology oncologic conditions, which include basal cell carcinoma and other dermatological oncology indications. The company has a collaboration and license agreement with Torii Pharmaceutical Co., Ltd. for the development and commercialization of its product candidates for the treatment of molluscum and common warts in Japan; and a license agreement with Lytix Biopharma AS to develop and commercialize VP-315 for use in malignant and pre-malignant dermatological indications. Verrica Pharmaceuticals Inc. was incorporated in 2013 and is headquartered in West Chester, Pennsylvania.
Verrica Pharmaceuticals to Present New YCANTH® Data Analysis at Two Upcoming Dermatology Conferences
Verrica Pharmaceuticals will present new pooled Phase 3 data on YCANTH at the Fall Clinical Dermatology Conference and the 2026 PeDRA Annual Conference in October.
The post-hoc analysis of CAMP-1 and CAMP-2 shows complete clearance of molluscum approximately 4 times faster than vehicle (HR=4.06), with Day 84 clearance rates of 60.1% versus 19.9%.
An encore poster will also describe exploratory abscopal-like effects of VP-315 in untreated basal cell carcinoma tumors from a Phase 2 study.