share_log

Coeptis Therapeutics to Present Its Universal Allogeneic SNAP-CAR NK Cell Therapy at the ISCT 2024

Coeptis Therapeutics to Present Its Universal Allogeneic SNAP-CAR NK Cell Therapy at the ISCT 2024

Coeptis Therapeutics 將在 2024 年 ISCT 上展示其通用同種異體 SNAP-CAR NK 細胞療法
Coeptis Therapeutics ·  05/08 00:00

WEXFORD, Pa., May 8, 2024 /PRNewswire/ -- Coeptis Therapeutics Holdings, Inc. (Nasdaq: COEP) (the "Company" or "Coeptis"), a biopharmaceutical company developing innovative cell therapy platforms for cancer, autoimmune, and infectious diseases, announced today that the Company has been selected for an oral presentation of the abstract titled Developing A First-In-Class Universal Allogeneic Snap-Car NK Cell Therapy at the International Society for Cell & Gene Therapy 2024, being held May 28th to June 1st in Vancouver, Canada.

賓夕法尼亞州韋克斯福德,2024 年 5 月 8 日/PRNewswire/— Coeptis Therapeutics Holdings, Inc.(納斯達克股票代碼:COEP)(“公司” 或 “Coeptis”)是一家爲癌症、自身免疫和傳染病開發創新細胞療法平台的生物製藥公司,今天宣佈,該公司已被選爲該摘要的口頭陳述 開發一流的通用異基因 Snap-Car NK 細胞療法 在5月28日舉行的2024年國際細胞與基因療法學會上第四 至 6 月 1 日st 在加拿大溫哥華。

The Company's SNAP-CAR platform technology has demonstrated its potential as a "universal" CAR therapy with the potential to target multiple antigens through combinatorial use of different adaptors, thus potentially avoiding toxicities and relapse due to antigen loss. In Q3 of 2023, Coeptis expanded its exclusive license agreement with the University of Pittsburgh for SNAP-CAR to include natural killer (NK) cells.

該公司的SNAP-CAR平台技術已證明其作爲 “通用” CAR療法的潛力,有可能通過組合使用不同的適配器來靶向多種抗原,從而有可能避免因抗原流失而產生毒性和復發。2023年第三季度,Coeptis擴大了與匹茲堡大學簽訂的SNAP-CAR獨家許可協議,將自然殺傷(NK)細胞包括在內。

The background and aim of the abstract revolve around chimeric antigen receptor (CAR) expression by engineered NK cells and the ability to improve their innate anti-tumor functions by specifically activating NK cells in the presence of tumor antigen. Backed by research performed in conjunction with the University of Pittsburgh and Deverra Therapeutics, allogeneic CAR NK cells may be a safer, more clinically accessible, and cost-effective cellular therapy than autologous CAR T-cells. Based on the demonstrated successful use of a novel SNAP-CAR technology in T-cells, the Company is developing a first-in-class universal allogeneic SNAP-CAR NK cell. This product replaces the antigen binding domain of a CAR with a SNAP tag enzyme that carries out a self-labeling reaction to covalently attach any antibody conjugated to a benzylguanine (BG) tag to create a functional antigen-specific CAR.

摘要的背景和目標圍繞工程化NK細胞的嵌合抗原受體(CAR)表達,以及在存在腫瘤抗原的情況下通過特異性激活NK細胞來改善其與生俱來的抗腫瘤功能的能力。在匹茲堡大學和Deverra Therapeutics聯合開展的研究的支持下,與自體CAR T細胞相比,異體CAR NK細胞可能是一種更安全、更具臨床可及性和成本效益的細胞療法。基於已證明在T細胞中成功使用一種新型SNAP-CAR技術,該公司正在開發同類首款通用異體SNAP-CAR NK細胞。該產品用 SNAP 標籤酶取代 CAR 的抗原結合域,該酶進行自標記反應,將任何與苯甲鳥嘌呤 (BG) 標籤偶聯的抗體共價附着,從而產生功能性抗原特異性 CAR。

"ISCT 2024 is a prestigious gathering renowned for fostering groundbreaking ideas and innovation," said Dave Mehalick, President and CEO of Coeptis Therapeutics. "Our presentation represents a significant and meaningful path forward in advancing our mission to develop a proprietary, allogeneic cell generation platform aimed at universalizing the treatment of many debilitating diseases."

Coeptis Therapeutics總裁兼首席執行官戴夫·梅哈利克表示:“ISCT 2024是一次享有盛譽的會議,以促進開創性的想法和創新而聞名。”“我們的演講代表了推進我們開發專有異基因細胞生成平台的使命的重要而有意義的前進道路,該平台旨在普及許多使人衰弱的疾病的治療。”

Details of the presentations are outlined below:

演講的細節概述如下:

TITLE: DEVELOPING A FIRST-IN-CLASS UNIVERSAL ALLOGENEIC SNAP-CAR NK CELL

標題: 開發出同類首創的通用異基因 SNAP-CAR NK 細胞

PRESENTATION TYPE: Oral, Thursday, May 30, 2024 at 8am

演示文稿類型: 口服,2024 年 5 月 30 日星期四上午 8 點

AUTHORS: Carrie Stoltzman, Erika von Euw, Braxton Jamison (presenting author), Emily Hsieh, Kevin Green, Lara Ionescu Silverman, Dan Yerace, Dave Mehalick, Colleen Delaney

作者: Carrie Stoltzman、Erika von Euw、Braxton Jamison(主持作者)、Emily Hsieh、Kevin Green、Lara Ionescu Silverman、Dan Yerace、Dave Mehalick、Colleen Delaney

INSTITUTIONS: Deverra Therapeutics, Seattle, WA, United States

機構: Deverra Therapeutics,美國華盛頓州西雅圖

Coeptis Therapeutics, Wexford, PA, United States

Coeptis 療法美國賓夕法尼亞州韋克斯福德

The International Symposium on Cell and Gene Therapy (ISCT) brings together leading researchers, clinicians and industry experts in cell and gene therapy from around the world. Serving as a nexus for collaboration, the conference promotes the exchange of new scientific advances, technological advances and clinical insights in the rapidly developing field of cell and gene therapy. For more information: www.isctglobal.org/isct2024.

國際細胞與基因療法研討會(ISCT)彙集了來自世界各地的細胞和基因療法領域的領先研究人員、臨床醫生和行業專家。作爲合作的紐帶,該會議促進了快速發展的細胞和基因療法領域的新科學進展、技術進步和臨床見解的交流。欲了解更多信息: www.isctglobal.org/isct2024

About Coeptis Therapeutics Holdings, Inc.
Coeptis Therapeutics Holdings, Inc., together with its subsidiaries including Coeptis Therapeutics, Inc. and Coeptis Pharmaceuticals, Inc., (collectively "Coeptis"), is a biopharmaceutical company developing innovative cell therapy platforms for cancer, autoimmune, and infectious diseases that have the potential to disrupt conventional treatment paradigms and improve patient outcomes. Coeptis' product portfolio and rights are highlighted by assets licensed from Deverra Therapeutics, including an allogeneic cellular immunotherapy platform and DVX201, a clinical-stage, unmodified natural killer cell therapy technology. Additionally, Coeptis is developing a universal, multi-antigen CAR T technology licensed from the University of Pittsburgh (SNAP-CAR), and the GEAR cell therapy and companion diagnostic platforms, which Coeptis is developing with VyGen-Bio and leading medical researchers at the Karolinska Institutet. Coeptis' business model is designed around maximizing the value of its current product portfolio and rights through in-license agreements, out-license agreements and co-development relationships, as well as entering into strategic partnerships to expand its product rights and offerings, specifically those targeting cancer and infectious diseases. The Company is headquartered in Wexford, PA. For more information on Coeptis visit https://coeptistx.com/.

關於 Coeptis Therapeutics Holdings
Coeptis Therapeutics Holdings, Inc. 及其子公司,包括Coeptis Therapeutics, Inc.和Coeptis Pharmicals, Inc.(統稱 “Coeptis”),是一家生物製藥公司,爲癌症、自身免疫和傳染病開發創新的細胞治療平台,這些平台有可能顛覆傳統治療模式並改善患者預後。Coeptis的產品組合和權利以Deverra Therapeutics許可的資產爲重點,包括異基因細胞免疫療法平台和臨床階段、未經修改的自然殺傷細胞療法技術 DVX201。此外,Coeptis正在開發一種獲得匹茲堡大學(SNAP-CAR)許可的通用多抗原CAR T技術,以及GEAR細胞療法和伴隨診斷平台,Coeptis正在與Vygen-bio和卡羅林斯卡研究所的領先醫學研究人員共同開發該平台。Coeptis的商業模式旨在通過許可協議、外包許可協議和共同開發關係最大化其當前產品組合和權利的價值,以及建立戰略合作伙伴關係以擴大其產品權利和供應,特別是針對癌症和傳染病的產品權利和供應。該公司總部位於賓夕法尼亞州韋克斯福德。有關 Coeptis 的更多信息,請訪問 https://coeptistx.com/

Cautionary Note Regarding Forward-Looking Statements
This press release and statements of our management made in connection therewith contain or may contain "forward-looking statements" (as defined in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended). Forward-looking statements include statements concerning our plans, objectives, goals, strategies, future events or performance, and underlying assumptions, and other statements that are other than statements of historical facts. When we use words such as "may," "will," "intend," "should," "believe," "expect," "anticipate," "project," "estimate" or similar expressions that do not relate solely to historical matters, we are making forward-looking statements. Forward-looking statements are not a guarantee of future performance and involve significant risks and uncertainties that may cause the actual results to differ materially and perhaps substantially from our expectations discussed in the forward-looking statements. Factors that may cause such differences include but are not limited to: (1) the inability to maintain the listing of the Company's securities on the Nasdaq Capital Market; (2) the risk that the integration of the Deverra licensed assets will disrupt current plans and operations of the Company; (3) the inability to recognize the anticipated benefits of the newly-licensed assets, which may be affected by, among other things, competition, the ability of the Company to grow and manage growth economically and hire and retain key employees; (4) the risks that the Company's products in development or the newly-licensed assets fail clinical trials or are not approved by the U.S. Food and Drug Administration or other applicable regulatory authorities; (5) costs related to integrating the newly-licensed Deverra assets and pursuing the contemplated asset development paths; (6) changes in applicable laws or regulations; (7) the possibility that the Company may be adversely affected by other economic, business, and/or competitive factors; and (8) the impact of the global COVID-19 pandemic on any of the foregoing risks and other risks and uncertainties identified in the Company's filings with the Securities and Exchange Commission (the "SEC"). The foregoing list of factors is not exclusive. All forward-looking statements are subject to significant uncertainties and risks including, but not limited, to those risks contained or to be contained in reports and other filings filed by the Company with the SEC. For these reasons, among others, investors are cautioned not to place undue reliance upon any forward-looking statements in this press release. Additional factors are discussed in the Company's filings made or to be made with the SEC, which are available for review at www.sec.gov. We undertake no obligation to publicly revise these forward-looking statements to reflect events or circumstances that arise after the date hereof unless required by applicable laws, regulations, or rules.

關於前瞻性陳述的警示說明
本新聞稿以及我們管理層就此發表的聲明包含或可能包含 “前瞻性陳述”(定義見經修訂的1933年《證券法》第27A條和經修訂的1934年《證券交易法》第21E條)。前瞻性陳述包括有關我們的計劃、目的、目標、戰略、未來事件或業績以及基本假設的陳述,以及除歷史事實陳述之外的其他陳述。當我們使用諸如 “可能”、“將”、“打算”、“應該”、“相信”、“期望”、“預期”、“項目”、“估計” 之類的詞語或不完全與歷史問題相關的類似表達方式時,我們是在做出前瞻性陳述。前瞻性陳述並不能保證未來的業績,涉及重大風險和不確定性,可能導致實際業績與我們在前瞻性陳述中討論的預期存在重大差異,甚至可能存在重大差異。可能導致此類差異的因素包括但不限於:(1)無法維持公司證券在納斯達克資本市場的上市;(2)整合Deverra許可資產有可能擾亂公司當前的計劃和運營;(3)無法確認新許可資產的預期收益,這可能會受到競爭、公司增長和增長能力等因素的影響經濟地管理增長,僱用和留住關鍵員工;(4)風險公司在開發的產品或新許可的資產未通過臨床試驗或未獲得美國食品藥品監督管理局或其他適用的監管機構的批准;(5)與整合新許可的Deverra資產和追求設想的資產開發道路有關的成本;(6)適用法律或法規的變化;(7)公司可能受到其他經濟、商業和/或競爭因素的不利影響;以及(8)的影響全球 COVID-19 疫情對上述任何風險及其他公司向美國證券交易委員會(“SEC”)提交的文件中發現的風險和不確定性。上述因素清單並不是排他性的。所有前瞻性陳述都存在重大的不確定性和風險,包括但不限於公司向美國證券交易委員會提交的報告和其他文件中包含或將包含的風險。出於這些原因,除其他外,提醒投資者不要過分依賴本新聞稿中的任何前瞻性陳述。公司向美國證券交易委員會提交或將要提交的文件中討論了其他因素,這些文件可在以下網址查閱 www.sec.gov。除非適用的法律、法規或規則要求,否則我們沒有義務公開修改這些前瞻性陳述以反映本陳述發佈之日之後發生的事件或情況。

Contacts
Coeptis Therapeutics, Inc.
IR@coeptistx.com

聯繫人
Coeptis Therapeutics, Inc
IR@coeptistx.com

SOURCE Coeptis Therapeutics, Inc.

來源 Coeptis Therapeutics, Inc.

声明:本內容僅用作提供資訊及教育之目的,不構成對任何特定投資或投資策略的推薦或認可。 更多信息
    搶先評論