Verrica’s Full Phase III Dataset In Molluscum Shows Greater Separation From Placebo

The latest Phase III data on Verrica’s formulation of cantharidin for the skin disease molluscum show a wider disparity from placebo.

Tablet with the medical specialty Dermatology on the display - Image

Verrica Pharmaceuticals Inc. aims to have the first FDA-approved drug therapy for molluscum contagiosum with a product that offers greater stability compared to compounded cantharidin, a quick on set of action and convenient application.

The Philadelphia-area firm presented full data from its pivotal Phase III CAMP-1 and CAMP-2 studies of VP-102 at the American

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Pipeline Watch: Six Approvals And Thirteen Phase III Readouts

Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.

Viatris Will File ‘Fast-Acting’ Meloxicam For FDA Approval This Year

 
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Seven years after acquiring it, Viatris will seek approval of a meloxicam formulation for acute pain backed by data from two Phase III studies in post-surgical pain settings.

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