Condition: Common Warts (Verruca Vulgaris) · Common Warts · Human Papilloma Virus (HPV) · Sponsor: Verrica Pharmaceuticals Inc.
People who participated in either the COVE-2 or COVE-3 study for common warts, may be eligible to enroll into this Long Term Follow Up (LTFU) study COVE-4. The main question(s) to answer in this LTFU study are: * To assess the safety of YCANTH (also known as VP-102 in the United Sates or TO-208 in Japan) by assessing concomitant medication use, and adverse events (AEs), including expected local skin reactions (LSRs). * To evaluate the efficacy of continued skin application of YCANTH (VP-102/TO-208) when applied to each common wart once every 21 days for a maximum of 4 additional treatments. Participants with eligible common warts present will receive YCANTH (VP-102/TO-208) with an interval of 21 (± 4) days between applications until there is a wart count of zero (ie, completed clearance has been achieved) or a maximum of 4 additional treatments. Participants with complete clearance will attend Observation Visits at intervals of 42 (± 4) days without treatment. Participants who develop a new wart after having a wart count of zero will resume Treatment Visits every 21 (± 4) days for a maximum of 4 additional treatments. All subjects will attend visits until the End-of-Study (EOS) Visit, which is on Day 378 (0/+ 8 days). If participants still have warts present after 4 additional treatments of YCANTH (VP-102/TO-208) the wart(s) will be discontinued from study and participants will be allowed to seek treatment but should be limited to destructive therapy such as cryosurgery an…
This description comes directly from the study's public registry record.
Project Manager · 484-453-3295 · 17340-COVE4@allucent.com
Always discuss trial participation with your own doctor first.
| Florida Center for Dermatology, P.A. | Saint Augustine, Florida, United States | Recruiting |
| The Indiana Clinical Trials Center, PC | Plainfield, Indiana, United States | Recruiting |
| Optima Research Boardman | Boardman, Ohio, United States | Recruiting |
| Texas Dermatology | San Antonio, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07457918