*Type C meeting held with FDA on clinical development plan for YCANTH's (VP-102) Common Warts indication on November 6, 2023. Meeting resulted in gaining alignment on the design of a pivotal Phase 3 development plan to evaluate YCANTH for the treatment of Common Warts. We sought additional guidance from the FDA in the second half of 2024 and anticipate Phase 3 trial could begin as early as mid-2025.
Common Warts
Common warts (verruca vulgaris) are contagious skin growths caused by a human papilloma virus (HPV). They represent one of the largest unmet needs in dermatology, with approximately 22 million cases in the United States. There are no FDA-approved treatments for common warts, which can be difficult to treat and negatively affect quality of life. Verrica has announced positive top-line results from its COVE-1 Phase 2 open-label clinical study of VP-102 for the treatment of common warts.
External Genital Warts
External genital warts are a viral skin disease caused by a human papilloma virus (HPV), which forms lesions on the surface of the skin on or near the genitals. HPV is the most common sexually transmitted infection in the United States. Verrica has announced positive top-line results from its CARE-1 Phase 2 study and intends to conduct additional studies of VP-102 for the treatment of external genital warts.