RecruitingPhase 3NCT07246590

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

COVE-2: A Phase 3, Double-blind, Randomized, Vehicle-controlled Study to Evaluate the Efficacy and Safety of YCANTH (VP-102) in Subjects With Common Warts (Verruca Vulgaris)


Sponsor

Verrica Pharmaceuticals Inc.

Enrollment

300 participants

Start Date

Dec 17, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 2 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying VP-102 and Vehicle for people with common warts, common warts (verruca vulgaris), and other related conditions. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 2 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

COMBINATION_PRODUCTVP-102

A single-use applicator and applied in sufficient quantity to cover the entirety of each treatable common wart, including approximately a 1 to 2 mm margin of surrounding, healthy skin. The contents of no more than 2 applicators may be applied at each treatment visit. Each applicator contains 0.45 mL of 0.7% w/v cantharidin. Occlusive tape (occlusive tape with similar properties should be used across all clinical sites) will be applied to warts that have been treated. Once applied, the occlusive tape should be gently rubbed to maximize adherence to the treated area.

COMBINATION_PRODUCTVehicle

Vehicle is contained in a single-use applicator and applied in sufficient quantity to cover the entirety of each treatable common wart, including approximately a 1 to 2 mm margin of surrounding, healthy skin. The contents of no more than 2 applicators may be applied at each treatment visit. The Vehicle applicator contains the same excipient formulation as the VP-102 applicator but does not contain the active pharmaceutical ingredient cantharidin. Occlusive tape (occlusive tape with similar properties should be used across all clinical sites) will be applied to warts that have been treated. Once applied, the occlusive tape should be gently rubbed to maximize adherence to the treated area.


Locations(6)

Florida Center for Dermatology, P.A.

Saint Augustine, Florida, United States

The Indiana Clinical Trials Center, PC

Plainfield, Indiana, United States

Anne Arundel Dermatology, PA dba Maryland Dermatology Laser Skin & Vein

Hunt Valley, Maryland, United States

Tennessee Clinical Research Center, Inc.

Nashville, Tennessee, United States

The University of Texas Health Science Center at Houston

Houston, Texas, United States

Texas Dermatology and Laser Specialists

San Antonio, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07246590


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