Key Takeaways:
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Of six patients administered with the therapy, four had complete tumor clearance at 49 days.
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Verrica is adding more sites to part two of the trial to hasten the asset’s development.
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Last month, the firm’s drug-device combination Ycanth was approved for molluscum.
Verrica Pharmaceuticals, Inc.’ first-in-class oncolytic peptide asset, VP-315, has shown efficacy signals in a Phase II trial in patients with basal cell carcinoma (BCC) just a month after the...
BCC is the most common form of skin cancer with an estimated 5.4 million new cases diagnosed in the US each year. VP-315 is designed to induce immunogenic cell death...
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