Revenue Growth
Total Q1 2026 revenue of $5.0M, including U.S. YCANTH product revenue of $4.3M, a 25.4% increase versus Q1 2025.
Strong Unit Dispensation Momentum
Q1 2026 U.S. YCANTH dispensed applicator units totaled 15,302, up 51.3% year-over-year; sequential increases vs Q4 2025 were +15.3% in revenue and +12.1% in units. March was the best monthly total since launch and April preliminary data improved further.
International Commercial Milestone — Japan Launch
Partner Torii (now a Shionogi subsidiary) launched YCANTH in Japan in February 2026; supply to Torii begins to offset Verrica's portion of common warts trial costs and Torii will fund the first $40M of trial costs.
Progress in Common Warts Phase III Program
Global Phase III program for common warts underway: first patient dosed in January, COVE-2 has achieved >50% of targeted enrollment and COVE-4 long-term follow-up has begun; COVE-3 targeted to initiate by mid-2026.
VP-315 Phase II Clinical Strength
VP-315 for basal cell carcinoma demonstrated a 97% objective response rate and an average 86% reduction in tumor size in Phase II, with over half of lesions achieving complete histological resolution; Phase III preparations and market research underway.
Regulatory and EU Pathway Progress
EMA CHMP provided positive feedback supporting an EU MAA filing for YCANTH for molluscum with no additional Phase III trials required, enabling progress toward an EU submission and potential commercialization partnerships.
Commercial Infrastructure and Adoption Enhancements
Launched YCANTH Rx (non-dispensing pharmacy/hub) to simplify benefits investigation and fulfillment; new Chief Commercial Officer in place; field force re-optimization underway to staff ~50 reps covering ~85% of TAM; >100,000 applicators dispensed since launch.