Verricaʼs lead product candidate, VP-102, is a proprietary drug-device combination that contains a GMP-controlled formulation of cantharidin (0.7% w/v) delivered via a single-use applicator that allows for precise topical dosing and targeted administration.

2023年2月27日 · VP-102 (cantharidin 0.7% Topical Solution) could potentially be the first FDA-approved treatment for molluscum contagiosum, a highly contagious viral skin infection affecting approximately 6 million people in the United States, primarily children.

2023年7月21日 · Until now, we finally have our very first FDA-approved product, Ycanth, which was known as VP-102, which is a drug-device combination product that applies a very small, precise amount of cantharidin and a surgical dye and is applied in-office to the patient's lesions.

VP-102 was a Patrol Squadron of the U.S. Navy. It was established as VP-18 on 1 September 1937, redesignated as VP-13 on 1 July 1939, redesignated as VP-26 on 11 December 1939, redesignated as VP-102 on 16 December 1940 and disestablished on 18 April 1942.

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2023年7月21日 · The US Food and Drug Administration (FDA) approved Verrica Pharmaceuticals’ drug candidate VP-102 (YCANTHE) for molluscum contagiosum treatment, making it the first treatment indicated for the viral-borne skin disease. 1

VP-102 is drug-device combination product containing cantharidin (0.7% w/v) and has undergone Phase III clinical trials for the treatment of molluscum contagiosum (molluscum). Efficacy and safety may differ by body region due to variable skin anatomy.

VP-102 is a proprietary drug-device combination containing cantharidin (0.7% w/v). This analysis examined the pooled safety and efficacy data from two phase 3 clinical trials of VP-102 for treating molluscum, by subject baseline age.

2020年9月23日 · What is the efficacy and safety of VP-102, a drug-device combination containing cantharidin, 0.7% (w/v), in individuals aged 2 years or older with molluscum contagiosum compared with vehicle?

Verricaʼs lead product candidate, VP-102, is a proprietary drug-device combination that contains a GMP-controlled formulation of cantharidin (0.7% w/v) delivered via a single-use applicator that allows for precise topical dosing and targeted administration.

VP-102 is a shelf-stable drug-device combination product that contains topical cantharidin (0.7% weight/volume [w/v]) and is being evaluated for the treatment of molluscum. Objectives: Our objective was to present pooled safety and efficacy analyses of VP-102 in the treatment of molluscum compared with vehicle.

2020年12月1日 · Treatment with VP-102 demonstrated superior efficacy to vehicle in the percentage of participants with complete clearance of MC lesions at the end of the study visit for CAMP-1 (VP-102: 46.3% vs vehicle: 17.9%; P < .001) and CAMP-2 (VP-102: 54.0% vs vehicle: 13.4%; P < .001).

2022年5月24日 · VP-102 could potentially be the first product approved by the FDA to treat molluscum contagiosum — a common, highly contagious skin disease that affects an estimated six million people in the United States, primarily children.

2021年2月18日 · VP-102 is a shelf-stable drug–device combination product that contains topical cantharidin (0.7% weight/volume [w/v]) and is being evaluated for the treatment of molluscum. Our objective was to present pooled safety and efficacy analyses of VP-102 in the treatment of molluscum compared with vehicle.

VP-102 addresses an unmet medical need to treat these serious skin lesions which can quickly spread among children and within families, and when left untreated, can lead to social stigma, anxiety, skin inflammation and secondary infections.”

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Verrica has announced positive top-line results from its COVE-1 Phase 2 open-label clinical trial of VP-102 for the treatment of verruca vulgaris, or common warts. The study included two cohorts that evaluated the safety and efficacy of VP-102 in patients with up to six warts.

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