YCANTH (cantharidin) by Verrica Pharmaceuticals. Approved for molluscum contagiosum, warts. First approved in 2023.
Drug data last refreshed 21h ago · AI intelligence enriched 1w ago
YCANTH (cantharidin) is a topical solution approved for molluscum contagiosum and warts, representing the first FDA-approved formulation of cantharidin for these indications. The drug works via direct application to lesions, inducing a blister response that facilitates removal of viral lesions. It addresses a significant unmet need in dermatology with a simple, office-based treatment paradigm.
Early-stage growth trajectory with modest competitive pressure suggests expanding field team and brand-building investment over next 3-5 years.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Long-Term Follow-up Study of Cantharidin (YCANTH [VP-102/TO-208]) in Patients With Common Warts (Verruca Vulgaris)
Cantharidin Application in Patients With Common Warts (Verruca Vulgaris) (COVE-2)
Cantharidin and Occlusion in Verruca Epithelium
Cantharidin Application in Molluscum Patients-1
Cantharidin Application in Molluscum Patients
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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.
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Upgrade to Pro — $25/moVerrica Pharmaceuticals is hiring 5 roles related to this product
YCANTH offers entry and mid-level opportunities primarily in field sales and territory management, reflecting early commercialization phase. Limited clinical pipeline means career growth is tied to market penetration and competitive displacement of liquid nitrogen, not indication expansion.
2 open roles linked to this drug