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Verrica Pharmaceuticals Inc. - VRCA STOCK NEWS

Welcome to our dedicated page for Verrica Pharmaceuticals news (Ticker: VRCA), a resource for investors and traders seeking the latest updates and insights on Verrica Pharmaceuticals stock.

Verrica Pharmaceuticals Inc., headquartered in West Chester, Pennsylvania, is a clinical-stage medical dermatology company dedicated to developing and commercializing innovative treatments for skin diseases. Founded in 2013, the company’s primary focus is on addressing unmet needs in dermatology through unique product candidates. Its lead product, YCANTH™ (cantharidin), is the first FDA-approved treatment for molluscum contagiosum, a highly contagious viral skin infection that primarily affects children.

The company’s flagship product, VP-102, is developed for the treatment of molluscum contagiosum and is currently in development for the treatment of common warts and external genital warts. VP-102 has successfully completed a Phase II clinical trial for common warts and a Phase I trial for genital warts. The innovative formulation of cantharidin in VP-102 provides precise topical dosing, making it a safe and effective solution for these conditions.

Verrica is also advancing another cantharidin-based product, VP-103, aimed at treating plantar warts. Furthermore, the company has a worldwide license agreement with Lytix Biopharma AS to develop and commercialize VP-315 (formerly LTX-315 and VP-LTX-315) for dermatologic oncology indications, including non-melanoma skin cancers such as basal cell carcinoma and squamous cell carcinoma.

In addition to its product development efforts, Verrica emphasizes strong partnerships and intellectual property strategies. The company has also recently amended its licensing agreement with Torii Pharmaceutical Co. Ltd. to jointly conduct a global pivotal Phase 3 clinical trial for common warts. This collaboration highlights Verrica’s commitment to expanding its product reach and addressing significant dermatological needs worldwide.

Verrica’s financial health is bolstered by its ongoing commercial operations and strategic agreements. The company’s recent achievements include securing a permanent J-code for YCANTH™ and receiving New Chemical Entity (NCE) status from the FDA, which grants a minimum of five years of regulatory exclusivity. These milestones are pivotal in driving the commercial success and adoption of YCANTH™ in the market.

For additional information and updates on Verrica Pharmaceuticals Inc., including recent news and investor relations, visit their website at www.verrica.com.

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Verrica Pharmaceuticals Inc. reports YCANTH™ revenue of $1.9M for Q4 and $4.7M for full year 2023. Over 200 million lives now covered by commercial insurance and managed Medicaid plans. The company continues to make progress with the launch of YCANTH™, securing a permanent J-Code for billing, and advancing pipeline with successful FDA meetings.
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Verrica Pharmaceuticals Inc. will participate in a fireside chat at the TD Cowen 44th Annual Healthcare Conference in Boston, Massachusetts on March 5, 2024. Investors can access a live webcast of the event on the Verrica website.
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Verrica Pharmaceuticals Inc. will host a conference call to discuss financial results for Q4 and full-year 2023, focusing on dermatology therapeutics. Participants can join via telephone or webcast.
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Verrica Pharmaceuticals Inc. has filed a lawsuit against Dormer Laboratories Inc. for false and misleading advertising of unapproved cantharidin-containing drugs in the US. Verrica seeks to enjoin Dormer Labs from marketing and selling these drugs and is also seeking compensatory, statutory, and punitive damages for violations of federal and Pennsylvania law. The lawsuit is in response to Dormer Labs' promotion of unapproved cantharidin-containing drugs to healthcare providers and customers, despite YCANTH being the only FDA-approved cantharidin-containing drug for molluscum contagiosum.
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Verrica Pharmaceuticals Inc. announced the issuance of a permanent J-Code for YCANTH™ by the Centers for Medicare & Medicaid Services (CMS), the only FDA-approved treatment for molluscum contagiosum. The J-Code will be fully published on April 1, 2024, expected to accelerate YCANTH utilization among U.S. Medicaid and Medicare patient populations. The permanent J-Code will streamline the billing and reimbursement process for YCANTH, reducing the risk of billing errors and allowing companies to receive pass-through payments through government-sponsored healthcare plans.
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Verrica Pharmaceuticals Inc. (Nasdaq: VRCA) announces completion of dosing for Part 2 of Phase 2 trial of VP-315 for the treatment of basal cell carcinoma. The company reiterates lesion clearance data expected in Q2 2024. Basal cell carcinoma affects 3-4 million people in the U.S. annually, with a high unmet need for new treatment options. VP-315 is a potential first-in-class oncolytic peptide designed to stimulate the immune system and destroy cancer cells, offering an alternative to surgery.
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Verrica Pharmaceuticals Inc. (Nasdaq: VRCA) received positive feedback from the FDA in a recent Type C meeting regarding the Phase 3 clinical development plan for YCANTH, a medication for common warts. The meeting led to mutual alignment with the FDA on the design of the Phase 3 study, indicating significant potential for YCANTH to address a sizable market opportunity. The company remains focused on addressing unmet needs in dermatology and is evaluating label expansion opportunities for YCANTH.
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Verrica Pharmaceuticals Inc. (VRCA) announced a distribution agreement with Walgreens to distribute YCANTH™, the first FDA-approved therapy for molluscum contagiosum, to millions of adults and children. The company aims to address the significant unmet medical need in dermatology by expanding its distribution network and working closely with Nufactor, its existing specialty pharmacy.
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Verrica Pharmaceuticals Inc. (Nasdaq: VRCA) announced that its partner, Torii Pharmaceutical Co., Ltd., reported positive top-line results from its Phase 3 trial of TO-208 (VP-102, marketed as YCANTH™) for the treatment of Molluscum Contagiosum in Japan. The trial showed statistically significant efficacy versus placebo, with well-tolerated results. Verrica and Torii signed an exclusive licensing agreement for the development and commercialization of VP-102 in Japan, taking a step closer to addressing the underserved patient population.
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VRCA: Verrica Pharmaceuticals to Present at Jefferies Global Healthcare Conference in London on November 15, 2023. Ted White, Verrica President & CEO, to discuss dermatology therapeutics development. Live webcast available on Verrica website.
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FAQ

What is the current stock price of Verrica Pharmaceuticals (VRCA)?

The current stock price of Verrica Pharmaceuticals (VRCA) is $0.6942 as of December 20, 2024.

What is the market cap of Verrica Pharmaceuticals (VRCA)?

The market cap of Verrica Pharmaceuticals (VRCA) is approximately 62.4M.

What is Verrica Pharmaceuticals Inc. known for?

Verrica Pharmaceuticals Inc. is known for developing and commercializing innovative treatments for dermatological conditions, including their lead product YCANTH™ for treating molluscum contagiosum.

What are the key products of Verrica Pharmaceuticals?

Key products include YCANTH™ (VP-102) for molluscum contagiosum, common warts, and external genital warts, as well as VP-103 for plantar warts and VP-315 for non-melanoma skin cancers.

Where is Verrica Pharmaceuticals headquartered?

Verrica Pharmaceuticals is headquartered in West Chester, Pennsylvania.

What recent achievements has Verrica Pharmaceuticals accomplished?

Recent achievements include the FDA approval of YCANTH™, securing a permanent J-code for YCANTH™, and receiving New Chemical Entity status from the FDA.

Who are Verrica Pharmaceuticals' key partners?

Key partners include Lytix Biopharma AS and Torii Pharmaceutical Co. Ltd., with whom Verrica has agreements for developing and commercializing their product candidates.

What is YCANTH™ used for?

YCANTH™ is used for the treatment of molluscum contagiosum, a highly contagious viral skin infection primarily affecting children. It is also in development for treating common warts and external genital warts.

What is the significance of the FDA's New Chemical Entity status for YCANTH™?

The NCE status provides YCANTH™ with a minimum of five years of regulatory exclusivity, enhancing its market protection and commercial potential.

What is the focus of Verrica Pharmaceuticals' clinical trials?

Current clinical trials focus on evaluating YCANTH™ for common warts and external genital warts, as well as developing VP-103 for plantar warts and VP-315 for non-melanoma skin cancers.

How does Verrica Pharmaceuticals contribute to dermatology?

Verrica Pharmaceuticals contributes to dermatology by developing novel treatments that address significant unmet needs in skin disease management, providing meaningful benefits to patients.

Where can I find more information about Verrica Pharmaceuticals?

More information about Verrica Pharmaceuticals can be found on their official website at www.verrica.com.

Verrica Pharmaceuticals Inc.

Nasdaq:VRCA

VRCA Rankings

VRCA Stock Data

62.39M
43.73M
43.73%
16.5%
9.89%
Biotechnology
Pharmaceutical Preparations
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United States of America
WEST CHESTER