NDATOPICALSOLUTION
Approved
Jul 2023
Lifecycle
Growth
Competitive Pressure
0/100
Clinical Trials
9
Data completeness
4/8 — Partial
Drug data last refreshed 5h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
YCANTH is a topical cantharidin solution approved in July 2023 for the treatment of skin lesions, particularly viral warts and molluscum contagiosum. Cantharidin is a naturally derived vesicant that induces blister formation, mechanically removing infected tissue. The product represents a non-invasive alternative to traditional destructive therapies.
Growth14.7 years to LOE
Early-stage growth trajectory with small commercial footprint; territory and account management roles indicate field-facing expansion phase.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (9)
Cantharidin Application in Patients With Common Warts (Verruca Vulgaris) (COVE-3)
Started Jun 2026
300 enrolled
Common WartsCommon Warts (Verruca Vulgaris)Human Papilloma Virus (HPV)+1 more
Long-Term Follow-up Study of Cantharidin (YCANTH [VP-102/TO-208]) in Patients With Common Warts (Verruca Vulgaris)
Started Mar 2026
600 enrolled
Common Warts (Verruca Vulgaris)Common WartsHuman Papilloma Virus (HPV)+1 more
Cantharidin Application in Patients With Common Warts (Verruca Vulgaris) (COVE-2)
Started Dec 2025
300 enrolled
Common WartsCommon Warts (Verruca Vulgaris)Human Papilloma Virus (HPV)+1 more
Cantharidin and Occlusion in Verruca Epithelium
Started Mar 2018
56 enrolled
Common WartWarts HandWarts+9 more
Cantharidin Application in Molluscum Patients-1
Started Mar 2018
266 enrolled
Molluscum Contagiosum
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.