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Verrica Provides Business and Operational Update

Verrica Provides Business and Operational Update

Verrica提供了業務和運營更新
GlobeNewswire ·  12/20 20:00

-- Dispensed applicator units in the fourth quarter of 2024 have exceeded the complete prior quarter even with significant cost reductions in sales and operational infrastructure

--儘管銷售和運營基礎設施的成本顯著降低,但2024年第四季度的分配塗抹器單元仍超過了上一季度的完整水平

-- Observed significant reduction in YCANTH distributor inventory levels

--觀察到 YCANTH 分銷商庫存水平顯著下降

-- New single applicator configuration for YCANTH expected to be available in the first quarter of 2025 to help meet growing product demand, reduce acquisition costs for physician practices and expand distribution and patient access

--YCANTH的新單一塗抹器配置預計將於2025年第一季度上市,以幫助滿足不斷增長的產品需求,降低醫生診所的購置成本,擴大分銷和患者可及性

-- Continue to advance pipeline of product candidates in common warts and basal cell carcinoma

--繼續推進常見疣和基底細胞癌的候選產品研發

WEST CHESTER, Pa., Dec. 20, 2024 (GLOBE NEWSWIRE) -- Verrica Pharmaceuticals Inc. ("Verrica" or the "Company") (Nasdaq: VRCA), a dermatology therapeutics company developing medications for skin diseases requiring medical interventions, today announced a business and operational update outlining the significant progress being made with respect to the new commercial strategy for YCANTH, Verrica's lead product for the treatment of molluscum contagiosum ("molluscum").

賓夕法尼亞州西切斯特,2024年12月20日(GLOBE NEWSWIRE)——開發需要醫療干預的皮膚病藥物的皮膚病治療公司維瑞卡製藥公司(「Verrica」 或 「公司」)(納斯達克股票代碼:VRCA)今天宣佈了業務和運營最新情況,概述了Verrica的主要軟體動物治療產品YCANTH的新商業戰略取得的重大進展傳染病(「軟體動物」)。

"Over the last several weeks since our November common stock offering, we have made significant progress across a number of key initiatives to help drive demand for YCANTH," said Jayson Rieger, PhD MBA, President and Chief Executive Officer of Verrica. "First and foremost, we are executing effectively on our previously announced commercial strategy for YCANTH, as evidenced by achievement of fourth quarter dispensed applicator units already surpassing dispensed applicator units in the prior quarter. We are growing the YCANTH business while implementing highly targeted cost management initiatives to prioritize spend that creates value and reducing or eliminating inefficient and unnecessary expenses. We are also pleased to note a significant reduction in YCANTH inventory levels from our distribution partners."

Verrica總裁兼首席執行官Jayson Rieger表示:「自11月普通股發行以來的過去幾週中,我們在許多關鍵舉措上取得了重大進展,以幫助推動對YCANTH的需求。」「首先,我們正在有效執行先前宣佈的YCANTH商業戰略,第四季度點膠器單元的成就已經超過了上一季度的點膠器單元,就證明了這一點。我們正在發展YCANTH業務,同時實施高度有針對性的成本管理計劃,以優先考慮創造價值的支出,減少或消除效率低下和不必要的支出。我們還高興地注意到,我們的分銷合作伙伴的YCANTH庫存水平顯著下降。」

Dr. Rieger continued, "We are responding to the growing patient demand for YCANTH by increasing our distribution capabilities, making YCANTH available to more dermatologists and pediatricians through our previous distribution channels as well as through local independent pharmacies. Furthermore, we expect to provide a single applicator packaging configuration for YCANTH in the first quarter of 2025, which we anticipate will provide an added level of convenience for our independent and specialty pharmacy network. We also expect that the single applicator packaging will facilitate initial purchases of the product by health care providers who prefer same day treatment for patients by requiring significantly less cash outlay under our buy-and-bill distribution model. Finally, we expect this new packaging may increase patient access by providing added optionality to buying groups, hospitals and government entities for including YCANTH on formulary to service their patients.

裏格博士繼續說:“我們正在通過提高我們的分銷能力,通過我們以前的分銷渠道以及當地的獨立藥房向更多的皮膚科醫生和兒科醫生提供YCANTH,來應對患者對YCANTH不斷增長的需求。此外,我們預計將在2025年第一季度爲YCANTH提供單一塗抹器封裝配置,我們預計這將爲我們的獨立和專業藥房網絡提供更大的便利。我們還預計,單一塗藥器包裝將大大減少我們的買入和賬單分配模式下所需的現金支出,從而促進醫療保健提供者首次購買該產品,他們更願意爲患者提供當日治療。最後,我們預計,這種新包裝將爲購買團體、醫院和政府實體提供更多選擇,讓他們將YCANTH納入處方集以爲患者提供服務,從而增加患者獲得的機會。

"As we enter 2025, we are excited about the opportunities that lie ahead for our company. As noted, we are already seeing favorable changes in the demand dynamics for YCANTH in response to our more focused and disciplined commercial strategy. Our recent financing also helped strengthen our balance sheet, while our ongoing efforts to improve Verrica's operational efficiencies will help preserve our capital resources."

「在我們進入2025年之際,我們對公司未來的機遇感到興奮。如前所述,我們已經看到YCANTH的需求動態發生了有利的變化,這是對我們更加集中、更嚴格的商業戰略的回應。我們最近的融資也有助於加強我們的資產負債表,而我們爲提高Verrica的運營效率所做的持續努力將有助於保護我們的資本資源。」

Dr. Rieger concluded, "We also believe that our pipeline opportunities provide a tremendous source of potential upside for our company. Together with our development partner, Torii Pharmaceutical, we continue to advance YCANTH (referred to as TO-208 in Japan) for the treatment of common warts, which represents the opportunity to address the single largest unmet medical need in dermatology. Additionally, encouraging preliminary data from our Phase 2 study suggests that our oncolytic peptide, VP-315, may have the potential to become a new and differentiated treatment approach for basal cell carcinoma. In summary, we have made significant progress over a short period of time, and Verrica is becoming a more focused and efficient commercial-stage company."

裏格博士總結道:「我們還相信,我們的管道機會爲我們公司提供了巨大的潛在上行空間。我們與我們的開發合作伙伴鳥居製藥一起,繼續推進用於普通疣治療的 YCANTH(在日本稱爲 TO-208),這爲解決皮膚病學領域最大的未滿足醫療需求提供了機會。此外,來自我們 2 期研究的令人鼓舞的初步數據表明,我們的溶瘤肽 VP-315 有可能成爲基底細胞癌的一種新的差異化治療方法。總而言之,我們在短時間內取得了重大進展,Verrica正在成爲一家更加專注和高效的商業階段公司。」

About YCANTH (VP-102)
YCANTH is a proprietary drug-device combination product that contains a GMP-controlled formulation of cantharidin delivered via a single-use applicator that allows for precise topical dosing and targeted administration for the treatment of molluscum. YCANTH is the first and only commercially available product approved by the FDA to treat adult and pediatric patients two years of age and older with molluscum contagiosum — a common, highly contagious skin disease that affects an estimated six million people in the United States, primarily children. Approval of YCANTH was based upon the positive results from two Phase 3 clinical trials in approximately 500 patients which demonstrated that YCANTH was a safe and effective therapeutic for the treatment of molluscum. Approximately 228 million lives are eligible to receive YCANTH covered by insurance. YCANTH is available to all patients with and without insurance coverage for $25 per treatment, and further financial assistance is available for patients in need. Please visit YCANTHPro.com for additional information.

關於 YCANTH (VP-102)
YCANTH 是一種專有的藥物器械組合產品,含有一種由 GMP 控制的斑點素配方,通過一次性塗抹器輸送,允許精確的局部給藥和有針對性的給藥,用於軟體動物的治療。YCANTH 是美國食品藥品管理局批准的第一款也是唯一一款用於治療兩歲及以上成人和兒科患者的市售產品。傳染性軟疣是一種常見的高度傳染性皮膚病,在美國估計有600萬人受到影響,主要是兒童。YCANTH的批准是基於對大約500名患者的兩項3期臨牀試驗的積極結果,這些試驗表明YCANTH是一種安全有效的軟體動物治療藥物。大約有22800萬人有資格獲得由保險承保的YCANTH。YCANTH適用於所有有和沒有保險的患者,每次治療費用爲25美元,有需要的患者可以獲得進一步的經濟援助。請訪問 Ycanthpro.com 獲取更多信息。

YCANTH should only be administered by a trained healthcare professional. YCANTH is not for home use.

YCANTH 只能由訓練有素的醫療保健專業人員管理。YCANTH 不適合家庭使用。

About Verrica Pharmaceuticals Inc.

關於 Verrica 製藥公司

Verrica is a dermatology therapeutics company developing medications for skin diseases requiring medical interventions. Verrica's product YCANTH (VP-102) (cantharidin), is the first and only commercially available treatment approved by the FDA to treat adult and pediatric patients two years of age and older with molluscum contagiosum, a highly contagious viral skin infection affecting approximately 6 million people in the United States, primarily children. YCANTH (VP-102) is also in development to treat common warts and external genital warts, two of the largest remaining unmet needs in medical dermatology. Verrica is developing VP-103, its second cantharidin-based product candidate, for the treatment of plantar warts. Verrica has also entered a worldwide license agreement with Lytix Biopharma AS to develop and commercialize VP-315 (formerly LTX-315 and VP-LTX-315) for non-melanoma skin cancers including basal cell carcinoma and squamous cell carcinoma. For more information, visit .

Verrica是一家皮膚病治療公司,爲需要醫療干預的皮膚病開發藥物。Verrica的產品YCANTH(VP-102)(cantharidin)是美國食品藥品管理局批准的第一種也是唯一一種市售療法,用於治療兩歲及以上的成人和兒童傳染性軟疣患者。傳染性軟疣是一種高度傳染性的病毒性皮膚感染,在美國影響約600萬人,主要是兒童。YCANTH(VP-102)也在開發中,用於治療普通疣和外生殖器疣,這是醫學皮膚病學中剩餘的最大未滿足的兩個需求。Verrica 正在開發 VP-103,這是其第二款基於角線素的候選產品,用於治療足底疣。Verrica還與Lytix Biopharma AS簽訂了全球許可協議,開發和商業化用於非黑色素瘤皮膚癌(包括基底細胞癌和鱗狀細胞癌)的 VP-315(前身爲 LTX-315 和 VP-LTX-315)。欲了解更多信息,請訪問。

Forward-Looking Statements
Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. These statements may be identified by words such as "believe," "expect," "may," "plan," "potential," "will," and similar expressions, and are based on Verrica's current beliefs and expectations. These forward-looking statements include statements about the availability of Verrica's single applicator packaging configuration and the benefits of such configuration, the commercialization of YCANTH, cost management initiatives and preservation of capital resources, and the clinical development and benefits of Verrica's product candidates, including YCANTH (VP-102). These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements. Risks and uncertainties that may cause actual results to differ materially include risks and uncertainties related to market conditions, satisfaction of customary closing conditions related to the proposed public offering and other risks and uncertainties that are described in Verrica's Annual Report on Form 10-K for the year ended December 31, 2023, Verrica's Quarterly Report on Form 10-Q for the quarter ended September 30, 2024 and other filings Verrica makes with the SEC. Any forward-looking statements speak only as of the date of this press release and are based on information available to Verrica as of the date of this release, and Verrica assumes no obligation to, and does not intend to, update any forward-looking statements, whether as a result of new information, future events or otherwise.

前瞻性陳述
根據1995年《私人證券訴訟改革法》的定義,本新聞稿中包含的任何未描述歷史事實的陳述均可能構成前瞻性陳述。這些陳述可以用 「相信」、「期望」、「可能」、「計劃」、「潛力」、「意願」 等詞語來識別,並基於Verrica當前的信念和期望。這些前瞻性陳述包括有關Verrica單一應用器包裝配置的可用性及其優勢、YCANTH的商業化、成本管理舉措和資本資源保護以及包括YCANTH(VP-102)在內的Verrica候選產品的臨牀開發和優勢的陳述。這些陳述涉及風險和不確定性,可能導致實際結果與此類陳述中反映的結果存在重大差異。可能導致實際業績出現重大差異的風險和不確定性包括與市場狀況相關的風險和不確定性、與擬議公開發行相關的慣例成交條件的滿意度以及Verrica截至2023年12月31日止年度的10-k表年度報告、Verrica截至2024年9月30日的季度10-Q表季度報告以及Verrica向美國證券交易委員會提交的其他文件中描述的其他風險和不確定性。任何前瞻性陳述僅代表截至本新聞稿發佈之日,並基於截至本新聞稿發佈之日Verrica獲得的信息,Verrica沒有義務也不打算更新任何前瞻性陳述,無論是由於新信息、未來事件還是其他原因。

FOR MORE INFORMATION, PLEASE CONTACT:

欲了解更多信息,請聯繫:

Investors:

投資者:

Kevin Gardner
LifeSci Advisors
kgardner@lifesciadvisors.com

凱文·加德納
LifeSCI 顧問
kgardner@lifesciadvisors.com

Chris Calabrese
LifeSci Advisors
ccalabrese@lifesciadvisors.com

克里斯·卡拉布雷斯
LifeSCI 顧問
ccalabrese@lifesciadvisors.com


譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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