Drug data last refreshed 33m ago · AI intelligence enriched 5d ago
YCANTH (cantharidin) is a topical solution approved by the FDA in July 2023 for the treatment of viral skin lesions, specifically common warts. It is a naturally derived compound that works through a blister-inducing mechanism to remove affected tissue. The product represents a non-invasive alternative to traditional wart removal methods.
Product is in peak commercial phase with established market entry; territory and account management roles indicate active field sales expansion.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Cantharidin Application in Patients With Common Warts (Verruca Vulgaris) (COVE-3)
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
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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 7 roles related to this product
YCANTH careers are concentrated in commercial field roles and manufacturing operations, reflecting early-stage market penetration with established supply chain needs. The 9 linked positions suggest a focused, lean team structure typical of specialty topical products in peak commercial phase.
9 open roles linked to this drug