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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 (NASDAQ: VRCA) reports positive momentum in Q4 2024, with YCANTH dispensed applicator units surpassing the previous quarter's numbers despite cost reductions. The company notes significant reduction in distributor inventory levels and plans to launch a single applicator configuration in Q1 2025 to enhance accessibility and reduce costs for physician practices.

The company is expanding distribution through local independent pharmacies while implementing targeted cost management. The new single applicator packaging aims to facilitate initial purchases and increase patient access through buying groups, hospitals, and government entities. Verrica continues to advance its pipeline, including YCANTH for common warts in partnership with Torii Pharmaceutical, and VP-315, an oncolytic peptide showing promising Phase 2 results for basal cell carcinoma treatment.

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Verrica Pharmaceuticals (Nasdaq: VRCA), a dermatology therapeutics company, has announced the granting of a nonqualified stock option to its new Chief Operating Officer, David Zawitz. The grant includes options to purchase 950,000 shares of common stock under the Company's Inducement Plan, effective December 9, 2024.

The stock option, granted as a material inducement to employment under Nasdaq Listing Rule 5635(c)(4), will have an exercise price equal to the closing price of Verrica's common stock on December 9, 2024. The vesting schedule includes 1/8th of shares after six months and 1/48th monthly thereafter, subject to continuous service.

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Verrica Pharmaceuticals announced that its partner Torii Pharmaceutical has submitted a New Drug Application (NDA) for TO-208 to treat Molluscum Contagiosum in Japan. TO-208, marketed as YCANTH® in the U.S., demonstrated superiority to vehicle in Phase 3 clinical studies with Japanese patients aged ≥2 years, showing a safety profile consistent with U.S. studies.

The development addresses an estimated 1.6 million cases of molluscum in Japan, representing a significant unmet medical need. This submission follows Torii's exclusive license agreement with Verrica in March 2021 for development and commercialization in Japan. Notably, VP-102 received U.S. approval in July 2023 and has been marketed as YCANTH® since August 2023.

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Verrica Pharmaceuticals (Nasdaq: VRCA) has announced the pricing of a $42.0 million public offering. The offering includes 44,964,045 shares of common stock and pre-funded warrants to purchase 2,235,955 shares. Additionally, the offering includes Series A warrants to purchase 23,600,000 shares at $1.0680 per share and Series B warrants for 23,600,000 shares at $1.3350 per share. The combined offering price is $0.89 per share with accompanying warrants. Jefferies is serving as the sole book-running manager, and the offering is expected to close on November 22, 2024.

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Verrica Pharmaceuticals (Nasdaq: VRCA), a dermatology therapeutics company, announced a proposed underwritten public offering of common stock and accompanying warrants. The offering includes an option for the underwriter to purchase up to 15% additional shares and/or warrants within 30 days. Jefferies is acting as the sole book-running manager. The offering will be conducted under a shelf registration statement filed with the SEC. The final size and terms are subject to market conditions.

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Verrica Pharmaceuticals reported negative net product revenue of $1.9M in Q3 2024, including a $1.7M provision for product returns. The company announced significant operational changes, including new leadership appointments of Dr. Jayson Rieger as CEO and John Kirby as Interim CFO. A restructuring effort reduced operating expenses by approximately 50% through territory optimization and headcount reduction. YCANTH dispensed applicator units increased to 7,706 in Q3 2024 from 5,975 in Q2. The company expects existing distributor inventory to support demand into Q1 2025. Cash position stands at $23M, projected to support operations into Q1 2025.

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Verrica Pharmaceuticals (NASDAQ: VRCA) announced positive preliminary results from Part 2 of their Phase 2 study for VP-315, a novel oncolytic peptide treatment for basal cell carcinoma (BCC). The study, involving 82 patients with 92 tumors, showed that 51% of treated tumors achieved complete histological clearance, while patients with residual tumors experienced an average 71% reduction in tumor size. The treatment demonstrated a favorable safety profile with no serious adverse events. Two abstracts featuring these results will be presented at the 2024 Fall Clinical Dermatology Conference. The company plans to request an FDA End-of-Phase 2 meeting in first half 2025, targeting the 3-4 million annual BCC cases in the U.S.

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Verrica Pharmaceuticals Inc. (Nasdaq: VRCA) has announced a significant restructuring of its commercial organization to reduce costs and expand access to YCANTH®, its treatment for molluscum contagiosum. The company plans to:

  • Reduce sales territories from 80 to approximately 35
  • Focus on territories with high molluscum prevalence, previous cantharidin users, and strong insurance coverage for YCANTH®
  • Expand sales efforts to include pediatricians in addition to dermatologists
  • Reduce headcount in certain support functions

These changes are expected to reduce the company's overall cost structure by approximately 50% while maintaining support for YCANTH® as the new standard of care for molluscum contagiosum. The restructuring will result in a one-time charge of approximately $1.0 million.

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Verrica Pharmaceuticals (Nasdaq: VRCA), a dermatology therapeutics company, announced its participation in the H.C. Wainwright 26th Annual Global Investment Conference in New York City. The event is scheduled for September 9-11, 2024. Ted White, President and CEO of Verrica, will engage in a fireside chat on Monday, September 9, 2024, at 1:30 pm ET.

Interested parties can access a live webcast of the event through a provided link or via the Investors/Presentations & Events section of Verrica's website. A replay of the webcast will be available for 90 days following the event, offering extended access to those unable to attend live.

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Verrica Pharmaceuticals (NASDAQ: VRCA) reported Q2 2024 financial results, highlighting $4.9M in YCANTH® revenue. The company expanded YCANTH's distribution through Cencora, Inc. and announced positive Phase 2 results for VP-315 in basal cell carcinoma treatment. Verrica is preparing for a global Phase 3 Common Warts trial, expected to start in 1H 2025. Key financial highlights include:

- Net product revenue: $4.9M
- Collaboration revenue: $0.3M
- Net loss: $17.2M ($0.37 per share)
- Cash and equivalents: $31.9M (as of June 30, 2024)

The company expects continued YCANTH prescription growth in H2 2024, driven by a permanent J-Code and expanded insurance coverage.

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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

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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