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VRCA News
VRCA Events
Verrica Q2 Revenue at $5.86M, Exceeds Expectations
Reports Q2 revenue $5.86M, consensus $5.74M. "Demand for YCANTH continues to accelerate, with dispensed applicator units reaching 19,626 for the quarter, up approximately 28% sequentially and 46% on a year-over-year basis, and representing our highest quarterly total since launch. We believe that our commercial strategy is working well and provides us with a growing confidence that YCANTH can become the standard of care for patients suffering from molluscum," said Jayson Rieger, President and Chief Executive Officer of Verrica.
Verrica Reports Q1 Revenue of $5.02M, Beating Consensus
Reports Q1 revenue $5.02M, consensus $4.52M. "Our first quarter performance reflects accelerating growth in market demand for YCANTH as the new standard of care for the treatment of molluscum contagiosum, a condition that impacts approximately 6 million people in the United States alone," said Jayson Rieger, president and CEO of Verrica. "As the only FDA-approved, HCP-administered therapy for molluscum, YCANTH is a product that is uniquely positioned to address the unmet need of patients with molluscum, largely children under the age of 14. Demand for YCANTH grew sharply during the first quarter, as we set new records for dispensed applicator units during the quarter and in the month of March. April dispensed applicator units increased further from the record total in March, and the Company has achieved the milestone of over 100,000 total dispensed applicator units since launch. We have also achieved another significant milestone in expanding to new markets as our partner, Torii Pharmaceutical, launched YCANTH in Japan for patients with molluscum following regulatory approval last year."
Verrica Reports Q4 Revenue of $5.092M, Beating Consensus
Reports 4Q revenue $5.092M, consensus $4.52M. "In 2025, Verrica successfully implemented a series of transformational changes that we believe have fundamentally improved the future growth and strategic value of our entire business," said Jayson Rieger, PhD, MBA, President and Chief Executive Officer of Verrica. "Our focused and efficient commercial strategy allowed us to nearly double dispensed applicator units of YCANTH from the prior year while cutting selling, general and administrative expenses by over 40% over that same period. This February, we dispensed more applicators of YCANTH per selling day than in any month in our history, reflecting strong and increasing demand for YCANTH. We are poised to advance our late-stage clinical pipeline in common warts and basal cell carcinoma, which collectively could represent a multiple billion-dollar opportunity. Finally, in 2025 we significantly improved our financial position, repaying our outstanding debt while extending our cash runway into the first quarter of 2027."
Verrica Pharmaceuticals Appoints Chris Chapman as Chief Commercial Officer
Verrica Pharmaceuticals announced the appointment of Chris Chapman as its Chief Commercial Officer. Most recently, Chapman served as Chief Commercial Officer at Dermavant Sciences
Verrica Pharmaceuticals Launches YCANTH in Japan with Torii Pharmaceutical
Verrica Pharmaceuticals "announced the launch of YCANTH in Japan by its partner, Torii Pharmaceutical Co. Ltd., a wholly-owned subsidiary of Shionogi & Co., Ltd., for the treatment of molluscum contagiosum. In September 2025, Verrica announced that Torii received approval from the Japanese Ministry of Health, Labour and Welfare ("MHLW") for YCANTH(R) (developed under the name TO-208) for the treatment of molluscum. Torii filed the New Drug Application for TO-208 in molluscum with MHLW in December 2024. Approval of YCANTH in Japan was based on positive top-line results from a confirmatory Phase 3 trial for the treatment of molluscum. The Phase 3 trial was conducted in Japan and was a double blind, randomized and parallel-group comparison study to evaluate the efficacy and safety of TO-208 in comparison to placebo, when applied once every 21 days for up to four applications in patients with molluscum. The top-line results from the trial showed that the proportion of subjects achieving complete clearance of all treatable molluscum lesions at the completion of the confirmatory study, the primary endpoint of efficacy, was statistically significant versus placebo. TO-208 was well tolerated during the study."
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