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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.

Rhea-AI Summary
Verrica Pharmaceuticals Inc. (VRCA) announced strong interest in prescribing YCANTH™ for molluscum treatment, covering over 112 million lives on commercial insurance and managed Medicaid plans. Financial results for Q3 2023 included $2.8 million net product revenue. The company also highlighted progress on the development pipeline, including VP-315 for basal cell carcinoma and VP-102 for common warts.
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Verrica Pharmaceuticals will host a conference call and webcast on November 9, 2023, to discuss its financial results for Q3 2023.
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Verrica Pharmaceuticals will host a virtual KOL event discussing the approval of YCANTH™ topical solution for molluscum contagiosum on Oct 11. YCANTH™ is the only FDA-approved product for treating molluscum in adults and pediatric patients. Molluscum affects approximately 6 million people in the US, primarily children. Without treatment, it can last up to 5 years.
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Verrica Pharmaceuticals CEO to participate in fireside chat at H.C. Wainwright conference
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Verrica Pharmaceuticals announces first commercial sale of YCANTH™, an FDA-approved treatment for molluscum, to exclusive distributor FFF Enterprises.
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Verrica supports FDA's action against unapproved molluscum contagiosum products
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Verrica Pharmaceuticals presented lesion clearance data from Part 1 of a Phase 2 study of VP-315 for the treatment of basal cell carcinoma (BCC). The study showed consistent clinical and histological clearance of treated BCC lesions with the 8 mg dose of VP-315, with 67% of subjects showing complete tumor clearance. The company plans to expand Part 2 of the trial based on these positive results.
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Verrica Pharmaceuticals Inc. (Nasdaq: VRCA) announces the acceptance of an abstract featuring clinical data from the ongoing Phase 2 study of VP-315 for the treatment of basal cell carcinoma (BCC). The presentation will highlight the antitumor efficacy of VP-315 as determined by clinical and histological lesion clearance. The data will be presented at the 2023 American Academy of Dermatology Innovation Academy from August 10-13, 2023, in Tampa, Florida.
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Verrica Pharmaceuticals Inc. (Nasdaq: VRCA) closed a $125 million debt financing with OrbiMed, receiving $50 million upfront and the potential for an additional $75 million based on revenue milestones. The funding will support the commercialization of YCANTH™, FDA-approved for molluscum contagiosum treatment. The five-year term loan bears interest based on the SOFR rate with a margin of 8% per annum. Verrica's cash runway is expected to extend into Q1 2025.
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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