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Medicus Pharma Ltd. Announces Minor Use (MUMS) Designation From the FDA for Doxorubicin-Containing Microneedle Array (D-MNA) Patch

Medicus Pharma Ltd. Announces Minor Use (MUMS) Designation From the FDA for Doxorubicin-Containing Microneedle Array (D-MNA) Patch

Medicus Pharma Ltd. 宣佈其多柔比星微針陣列(D-MNA)貼片獲得FDA的小規模使用(MUMS)認定。
newsfile ·  12/12 20:30

Company to Submit Product Development Plan to Treat External Squamous Cell Carcinoma (SCC) in Horses

公司將提交針對馬外部鱗狀細胞癌(SCC)的產品開發計劃

Toronto, Ontario and Philadelphia, Pennsylvania--(Newsfile Corp. - December 12, 2024) - Medicus Pharma Ltd. (NASDAQ: MDCX) (TSXV: MDCX) ("Medicus" or the "Company") is pleased to announce that its Investigational New Animal Drug (INAD File No.013880) has received Minor Use in Major Species Designation ("MUMS") from the U.S. Food and Drug Administration ("FDA") for its dissolvable Doxorubin-containing microneedle array (D-MNA) to treat external squamous cell carcinoma (SCC) in horses. The company received a notification from the FDA on December 9th 2024.

加拿大安大略省多倫多和美國賓夕法尼亞州費城--(資訊文件CORP - 2024年12月12日)- Medicus Pharma Ltd.(納斯達克:MDCX)(TSXV:MDCX)("Medicus"或"公司")欣然宣佈,其實驗性新動物藥品(INAD文件編號013880)已獲得美國食品藥品管理局("FDA")的主要物種小規模使用認證("MUMS"),用於治療馬的外部鱗狀細胞癌(SCC)的可溶性多索沙星微針陣列(D-MNA)。公司於2024年12月9日收到FDA的通知。

MUMS is a status similar to Orphan Drug status for human drugs. It entitles the company to an extended 7-year period of exclusive marketing following approval or conditional approval, provided that the company meets all requirements for maintaining the designation.

MUMS是一種類似於人用藥品的孤兒藥狀態的認證,允許公司在獲批或條件獲批後享有長達7年的獨佔市場資格,前提是公司滿足所有保持該認證的要求。

"In a relatively short period of time, we have made remarkable progress with the FDA in advancing the clinical development program of the veterinary application of our novel D-MNA patch in treating SCC in horses," stated Dr. Raza Bokhari, Executive Chairman & CEO. "Developing a non-invasive treatment for equine SCC represents an untapped market opportunity that we are excited to pursue. The MUMS designation is an important catalyst to provide us a first mover advantage and also position us to possibly have a commercially viable product as early as 2026."

"在相對較短的時間內,我們已在推進針對馬SCC的獸用應用的新型D-MNA貼片的臨床開發計劃與FDA取得了顯著進展,"執行董事會主席兼首席執行官Dr. Raza Bokhari表示。"開發一種非侵入性治療馬SCC的方法代表了一個尚未開發的市場機會,我們對此感到興奮。MUMS認證是爲我們提供首發優勢的重要催化劑,並使我們有可能在2026年儘早擁有商業化產品。"

Doxorubicin-containing microneedle array (D-MNA) is a patent protected dissovable transdermal patch with cellulose based microneedle arrays that are tip-loaded with doxorubicin. After application, the microneedles function by penetrating the strateum corneum layer of the skin, create a temporary microchannel, penetrate the tumor, dissolve and release doxorubicin into the target tumor, and eradicate the cancer cells.

含多索沙星的微針陣列(D-MNA)是一種受專利保護的可溶性經皮貼片,採用以纖維素爲基礎的微針陣列,針頭裝載多索沙星。貼片應用後,微針通過穿透皮膚表皮層,創造一個臨時微通道,穿透腫瘤,溶解並釋放多索沙星至目標腫瘤,滅活癌細胞。

Squamous Cell Carcinoma (SCC) in Horses

馬的鱗狀細胞癌(SCC)

SCC is a mucocutaneous skin tumor in horses, primarily affecting adult or aged horses with white or partially white coats. Breeds like Appaloosa, Belgian, American Paint, and Pinto are particularly susceptible. SCC often develops in areas with minimal pigmentation and sparse hair, notably around mucous membranes. More specifically, tumors are mainly seen around the eyes, lips, nose, anus, and external genitalia. The overall incidence of SCC is 2-3% and recent estimates of the US horse population range from 6.6 to 7.25 million horses.

SCC是馬的一種粘膜皮膚腫瘤,主要影響成年或老年馬,尤其是白色或部分白色毛髮的馬。像阿帕盧薩、比利時、美國斑馬和班圖馬等品種特別容易受到影響。SCC通常出現在色素極少和毛髮稀疏的區域,尤其是在粘膜周圍。更具體地說,腫瘤主要出現在眼睛、嘴脣、鼻子、肛門和外生殖器周圍。SCC的總體發生率爲2-3%,最近的美國馬匹數量估計在660,000到725萬之間。

Current treatment includes surgery to remove the largest mass, cryotherapy of the smaller mass, and local injection of a chemotherapy drug. In some cases, a topical chemotherapeutic drug will be prescribed in the form of drops (tumors near the eye) or cream (tumors in other parts of body). Additionally, some horses are put on an oral drug called piroxicam that may slow the return of the cancerous cells.

當前治療包括手術去除最大腫瘤,對小腫瘤進行冷凍療法,以及局部注射化學治療藥物。在某些情況下,可能會開具局部化學治療藥物,以滴劑(眼睛附近的腫瘤)或乳膏(身體其他部位的腫瘤)形式使用。此外,一些馬匹可能會口服一種叫做吡羅昔康的藥物,這可能會減緩癌細胞的復發。

For further information contact:

如需更多信息,請聯繫:

Carolyn Bonner, President
(610) 636-0184
cbonner@medicuspharma.com

卡羅琳·博納,主席
(610) 636-0184
cbonner@medicuspharma.com

Jeremy Feffer
LifeSci Advisors
(212) 915-2568
jfeffer@lifesciadvisors.com

傑雷米·費弗
LifeSci顧問
(212) 915-2568
jfeffer@lifesciadvisors.com

About Medicus Pharma Ltd:

關於Medicus Pharma Ltd:

Medicus Pharma Ltd. (NASDAQ: MDCX) (TSXV: MDCX) is a biotech/life sciences company focused on accelerating the clinical development programs of novel and disruptive therapeutics assets.

Medicus Pharma Ltd.(納斯達克:MDCX)(TSXV:MDCX)是一家生物科技/生命科學公司,致力於加速新型和顛覆性治療資產的臨床開發項目。

SkinJect Inc. a wholly owned subsidiary of Medicus Pharma Ltd, is a development stage, life sciences company focused on commercializing novel, non-invasive treatment for basal cell skin cancer using patented dissolvable microneedle patch to deliver chemotherapeutic agent to eradicate tumors cells. The Company has completed a phase 1 safety & tolerability study (SKNJCT-001) in March of 2021, which met its primary objective of safety and tolerability; the study also describes the efficacy of the investigational product D-MNA, with six (6) participants experiencing complete response on histological examination of the resected lesion. The Company submitted a Phase 2 IND clinical protocol to the FDA in January 2024 for a randomized, controlled, double-blind, multicenter clinical study (SKNJCT-003) that is expected to randomize up to 60 patients. The study is designed to evaluate the efficacy of two dose of two dose levels (100 and 200 ug) of D-MNA compared to placebo (P-MNA) in subjects with nodular BCC. Patient recruitment is currently underway in nine sites across the United States.

SkinJect Inc.是Medicus Pharma Ltd.的全資子公司,作爲一家開發階段的生命科學公司,專注於商業化新型非侵入性治療基礎細胞皮膚癌,使用專利的可溶性微針貼片將化療藥物遞送至腫瘤細胞以消滅腫瘤。該公司於2021年3月完成了一項1期安全性和耐受性研究(SKNJCt-001),達到了安全性和耐受性的主要目標;該研究還描述了調查產品D-MNA的療效,六(6)名參與者在切除病變的組織學檢查中顯示完全反應。該公司於2024年1月向FDA提交了一項2期IND臨床協議,進行一項隨機、對照、雙盲、多中心臨床研究(SKNJCt-003),預計將隨機選擇多達60名患者。該研究旨在評估兩種劑量水平(100和200微克)D-MNA與安慰劑(P-MNA)在結節性BCC患者中的療效。患者招募目前正在美國九個地點進行。

Cautionary Notice on Forward-Looking Statements

關於前瞻性聲明的警告通知

Certain information in this news release constitutes "forward-looking information" under applicable securities laws. "Forward-looking information" is defined as disclosure regarding possible events, conditions or financial performance that is based on assumptions about future economic conditions and courses of action and includes, without limitation, statements regarding the Company's plans and expectations concerning, and future outcomes relating to, its product development plans and clinical development programs, including improvements thereto and the timing thereof, and approval from the FDA and the timing thereof. Forward-looking statements are often but not always, identified by the use of such terms as "may", "might", "will", "will likely result", "would", "should", "estimate", "plan", "project", "forecast", "intend", "expect", "anticipate", "believe", "seek", "continue", "target" or the negative and/or inverse of such terms or other similar expressions.

本新聞稿中的某些信息構成根據適用證券法的「前瞻性信息」。「前瞻性信息」被定義爲基於對未來經濟條件和行動方向的假設而披露的可能事件、條件或財務表現的信息,包括但不限於,關於公司的計劃和預計情況,以及與其產品開發計劃和臨床開發項目相關的未來結果,包括對此的改進及其時間,及FDA的批准及其時間的聲明。前瞻性聲明通常但並非總是通過使用「可能」、「也許」、「將」、「可能將導致」、「將會」、「應該」、「估計」、「計劃」、「項目」、「預測」、「打算」、「期望」、「預見」、「相信」、「尋求」、「繼續」、「目標」或這些術語的否定和/或相反形式或其他類似表達來識別。

These statements involve known and unknown risks, uncertainties and other factors, which may cause actual results, performance or achievements to differ materially from those expressed or implied by such statements, including those risk factors described in the Company's public filings on SEDAR+ and on EDGAR, which may impact, among other things, the trading price and liquidity of the Company's common shares. Forward-looking statements contained in this news release are expressly qualified by this cautionary statement and reflect our expectations as of the date hereof, and thus are subject to change thereafter. The Company disclaims any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.

這些陳述涉及已知和未知的風險、不確定性及其他因素,這些因素可能導致實際結果、表現或成就與這些陳述所表達或暗示的情況有重大差異,包括在公司在SEDAR+和EDGAR上公開的文件中描述的風險因素,這可能影響公司的普通股的交易價格和流動性。本新聞稿中包含的前瞻性陳述明確受到這一警示性聲明的限制,並反映我們截至本日期的期望,因此此後可能會發生變化。公司不承擔對任何前瞻性陳述進行更新或修訂的意圖或義務,無論是因新信息、未來事件或其他原因,除非法律要求。

Readers are cautioned that the foregoing list is not exhaustive and readers are encouraged to review the Company's long form prospectus accessible on the Company's profile on SEDAR+ at and on EDGAR at www.sec.gov. Readers are further cautioned not to place undue reliance on forward-looking statements as there can be no assurance that the plans, intentions or expectations upon which they are placed will occur. Such information, although considered reasonable by management at the time of preparation, may prove to be incorrect and actual results may differ materially from those anticipated.

提醒讀者,前述列表並非詳盡無遺,並鼓勵讀者查閱公司在SEDAR+上的長形式招股說明書及在EDGAR上的資料(網址:www.sec.gov)。此外,提醒讀者不要對前瞻性陳述過於依賴,因爲無法保證所依據的計劃、意圖或期望會實現。儘管在準備時管理層認爲這些信息是合理的,但可能會證明是錯誤的,實際結果可能與預期有重大差異。

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

TSX Venture Exchange及其監管服務提供者(如該術語在TSX Venture Exchange規定中所定義的)不對本新聞稿的充分性或準確性承擔責任。

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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