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Cantharidin Application in Patients With Common Warts (Verruca Vulgaris) (COVE-2)

Study acronym: COVE-2
StatusRecruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗

Record History

  1. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 3 to 6
    • Start date changed from estimate of Dec 2025 to Dec 17, 2025
    v2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a Phase 3, double-blind, randomized, vehicle-controlled study (Study number VP-CW-301; referred to as COVE-2 \[Cantharidin and Occlusion in Verruca Epithelium\]) to evaluate the efficacy and safety of YCANTH (VP-102) treatment in subjects with common warts.
Trial Details
NCT Number NCT07246590
Lead Sponsor Verrica Pharmaceuticals Inc.
Collaborators: Canfield Scientific Inc., Medidata Solutions, Veeva Systems, Torii Pharmaceutical Co. Ltd., Allucent (US) LLC, Myonex LLC
Conditions
(from sponsor)		 Common Warts, Common Warts (Verruca Vulgaris), Human Papilloma Virus (HPV), Warts
Related terms Warts
Enrollment 300 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov