Biopharma Transcript

Verrica Pharmaceuticals Inc. VRCA

Nasdaq · Phase 3 · dermatology · device-combination · EDGAR · Updated Oct 24, 2026

Verrica Pharmaceuticals Inc. (Nasdaq: VRCA) is a dermatology drug developer. Its lead program, YCANTH (VP-102, cantharidin), is in Phase 3 for Molluscum contagiosum. Its next catalyst on record is YCANTH (common warts): Phase 3 top-line data (2027).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: YCANTH (common warts) — Phase 3 top-line data (2027). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
YCANTH (VP-102)Molluscum contagiosumdevice-combinationApproved
VP-102 (COVE-2, COVE-3, COVE-4)Common wartsdevice-combinationPhase 3
VP-315Basal cell carcinomabiologic-otherPhase 2

Recent results and decisions

  1. Jun 22, 2026
    started First U.S. patient dosed June 22, 2026 in second Phase 3 trial (COVE-3) of YCANTH in common warts.On June 22, 2026, the Company announced that the first U.S. patient was dosed in the second pivotal clinical trial (COVE-3) in its global Phase 3 program evaluating YCANTH® (VP-102) for the treatment of common warts in the US and Japan. Filing
  2. Mar 11, 2026
    positive New abscopal analysis: 3 of 14 observed-but-untreated lesions had complete histologic clearance and tumor size fell 67% across all 14.Specifically, 3 out of the 14 lesions had complete histologic clearance and there was a 67% overall reduction in tumor size across all 14 lesions. Filing
  3. Dec 1, 2025
    started First patient dosed in December 2025 in first Phase 3 trial (COVE-2) of YCANTH in common warts.On January 7, 2026, the Company announced that the first patient was dosed in December 2025 in the global Phase 3 program evaluating YCANTH (VP-102) for the treatment of common warts. Filing

1 more on record.

For subscribers

Other phase 3 dermatology companies