Clinical Trial

Cantharidin Application in Patients With Common Warts (Verruca Vulgaris) (COVE-3)

Study acronym: COVE-3
Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
This is a Phase 3, double-blind, randomized, vehicle-controlled study (Study number VP-CW-302; referred to as COVE-3 \[Cantharidin and Occlusion in Verruca Epithelium\]) to evaluate the efficacy and safety of YCANTH (VP-102/TO-208) treatment in subjects with common warts.
Trial Details
NCT Number NCT07637734
Lead Sponsor Verrica Pharmaceuticals Inc.
Collaborators: Torii Pharmaceutical Co. Ltd., CMIC Co, Ltd. Japan, Canfield Scientific Inc., Medidata Solutions, Veeva Systems, Allucent (US) LLC, Myonex LLC
Conditions Common Warts, Common Warts (Verruca Vulgaris), Human Papilloma Virus (HPV), Warts
Enrollment 300 participants
Start Date 2026-06
Primary Completion 2027-08 (estimated)
Study Completion 2027-10 (estimated)
Updated on ClinicalTrials.gov 2026-06-10