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Coeptis Therapeutics to Pursue Phase 2 Program Using Proprietary First-in-Class Allogeneic NK Cell Therapy for the Treatment of Viral Infections

Coeptis Therapeutics to Pursue Phase 2 Program Using Proprietary First-in-Class Allogeneic NK Cell Therapy for the Treatment of Viral Infections

Coeptis Therapeutics將使用專有的同類首創異體NK細胞療法進行第二階段計劃來治療病毒感染
Coeptis Therapeutics ·  02/07 13:00

Novel NK cell therapy approach is designed to bolster and replenish the immune system during severe viral infection, which can severely reduce immune cells leading to hospitalization and death

新型 NK 細胞療法旨在增強和補充嚴重病毒感染期間的免疫系統,這會嚴重降低免疫細胞,導致住院和死亡

WEXFORD, Pa., Feb. 7, 2024 /PRNewswire/ -- Coeptis Therapeutics Holdings, Inc. (Nasdaq: COEP) (the "Company" or "Coeptis"), a biopharmaceutical company developing innovative cell therapy platforms for cancer and infectious diseases, today announced plans to pursue DVX201, its proprietary allogeneic stem cell expansion and directed differentiation platform of unmodified natural killer (NK) cell therapy, as an antiviral treatment addressing various respiratory viral infections that lead to hospitalization, including the "tripledemic" of influenza, COVID-19 and respiratory syncytial virus (RSV).

賓夕法尼亞州韋克斯福德,2024 年 2 月 7 日/PRNewswire/— 開發癌症和傳染病創新細胞療法平台的生物製藥公司Coeptis Therapeutics Holdings, Inc.(納斯達克股票代碼:COEP)(“公司” 或 “Coeptis”)今天宣佈計劃開發其專有的異基因幹細胞擴張和未改性自然殺傷(NK)細胞療法定向分化平台 DVX201,作爲一種抗病毒療法,用於治療導致住院的各種呼吸道病毒感染,包括流感、COVID-19 和呼吸道合胞病毒(RSV)的 “三重流行”。

DVX201, the first-ever allogeneic, cord-blood derived NK cell therapy generated from pooled donor CD34+ hematopoietic stem and progenitor cells (HSPC) cells, is designed to supply a boost of healthy immune cells to potentially help fight the infection by directly infusing them into the patient's body.

DVX201 是有史以來第一種由捐贈者 CD34+ 造血幹細胞和祖細胞 (HSPC) 合成的異基因、臍帶血衍生的 NK 細胞療法,旨在增強健康的免疫細胞,通過直接將免疫細胞注入患者體內,可能有助於抵抗感染。

DVX201 NK cells are generated from cord blood cells (from birth tissue), a well understood and FDA regulated source of cells, that has been infused into patients for over 20 years. DVX201 is produced by pooling CD34+ cells isolated from multiple cord blood donations to increase lot size and immune system diversity. Importantly, doses undergo stringent testing including a potency assay before treatment, to assess their ability to kill virally infected cells. Additionally, DVX201 does not contain T-cells, which significantly reduces the possibility for major rejection by patients, which is a major concern for some cell therapy products.

DVX201 NK 細胞由臍帶血細胞(來自出生組織)產生,臍帶血細胞是一種衆所周知並受美國食品藥品管理局監管的細胞來源,已被注入患者體內已有 20 多年。DVX201 是通過彙集從多次臍帶血捐贈中分離出來的 CD34+ 細胞來產生的,以增加批量和免疫系統的多樣性。重要的是,劑量在治療前要經過嚴格的測試,包括效力測定,以評估其殺死病毒感染細胞的能力。此外,DVX201 不含有 T 細胞,這顯著降低了患者出現嚴重排斥反應的可能性,這是一些細胞療法產品的主要問題。

"We're excited to progress the clinical development of this therapy to test a truly novel approach, treating severe viral infections with live cells to replenish and bolster patients' immune systems," said Colleen Delaney, MD, MSc, Chief Scientific and Medical Officer. "An important aspect of viral infections that are often observed in patients hospitalized with viruses like the flu, COVID-19, and RSV, often referred to as the tripledemic, is the challenges they present to immune cells. The immune system works hard to kill virally infected cells but, in many cases, struggle to keep up and become depleted, leading to severe infection, worsening symptoms, hospitalizations, and even death."

首席科學和醫學官科琳·德萊尼醫學博士、理學碩士科琳·德萊尼說:“我們很高興能夠推進這種療法的臨床開發,以測試一種真正的新方法,用活細胞治療嚴重的病毒感染,以補充和增強患者的免疫系統。”“在感染流感、COVID-19 和呼吸道合胞病毒等病毒(通常被稱爲三聯疫情)住院的患者中經常觀察到的病毒感染的一個重要方面是它們對免疫細胞構成的挑戰。免疫系統很難殺死病毒感染的細胞,但在許多情況下,它們難以跟上步伐並耗盡,從而導致嚴重感染、症狀惡化、住院甚至死亡。”

Dr. Delaney added: "Our first step is to fully explore key safety measures because this is a very novel approach to treating hospitalized viral infections with a first-in-class universal therapy. We have started dosing DVX201 at low doses and escalated upwards to almost 1 billion cells in a single infusion. For context, the body normally has around two billion NK cells at any given moment."

德萊尼博士補充說:“我們的第一步是充分探索關鍵的安全措施,因爲這是一種使用同類首創的通用療法治療住院病毒感染的非常新穎的方法。我們已經開始以低劑量給藥 DVX201,並在單次輸注中逐漸增加到近 10 億個細胞。就背景而言,人體通常在任何給定時刻都有大約20億個NK細胞。”

In two Phase 1 clinical trials for the treatment of relapsed/refractory acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS) and patients hospitalized with COVID-19 infection, interim data for a total of 17 patients and 25 infusions of DVX201 have indicated that the NK cell therapy is well-tolerated with no dose limiting toxicities (DLTs). Further, there have been no observed cytokine release syndrome (CRS) or infusion toxicities thus far, even through the highest dose level.

在兩項治療復發/難治性急性髓系白血病 (AML) 或高危骨髓增生異常綜合徵 (MDS) 和因 COVID-19 感染住院的患者的 1 期臨床試驗中,共有 17 名患者和 25 次 DVX201 輸液的中期數據表明,NK 細胞療法耐受性良好,沒有劑量限制毒性 (DLT)。此外,迄今爲止,即使在最高劑量水平下,也沒有觀察到細胞因子釋放綜合徵(CRS)或輸液毒性。

"Based on these favorable Phase 1 results to date, we are excited to advance plans for a Phase 2 clinical program investigating DVX201 as an anti-viral therapy in high-risk patients hospitalized with viral respiratory infections," said Dave Mehalick, President and CEO of Coeptis Therapeutics. "The tripledemic of flu, RSV, and COVID represents a serious challenge for our healthcare system for the foreseeable future. When vaccinations aren't sufficient and/or when vaccination rates are below levels necessary to stave off future epidemics, we believe this NK cell therapy approach has the potential to be an important treatment, either as monotherapy or in a complementary approach for severe infections. DVX201, the first-ever allogeneic, cord-blood derived NK cell therapy generated from pooled donor CD34+ HSPC cells, has the potential to offer significant support to patients and to our strained healthcare system."

Coeptis Therapeutics總裁兼首席執行官戴夫·梅哈利克表示:“基於迄今爲止這些良好的1期結果,我們很高興能夠推進一項2期臨床計劃的計劃,該項目旨在研究 DVX201 作爲一種抗病毒療法,用於治療因病毒性呼吸道感染住院的高危患者。”“在可預見的將來,流感、呼吸道合胞病毒和COVID的三重流行對我們的醫療系統構成了嚴峻的挑戰。當疫苗接種不足和/或疫苗接種率低於避免未來流行病所需的水平時,我們認爲這種NK細胞療法有可能成爲一種重要的治療方法,既可以作爲單一療法,也可以作爲嚴重感染的補充方法。DVX201 是有史以來第一種由捐贈者 CD34+ HSPC 細胞合成的異體臍帶血衍生的 NK 細胞療法,有可能爲患者和我們緊張的醫療保健系統提供重要支持。”

Since the COVID-19 pandemic, seasonal infections for the three viral infections have been elevated, and the CDC highlights last year's 2022-2023 "tripledemic" in which weekly hospitalization rates exceeded 20 per 100,000. If this season follows with a severe flu and RSV, and with a moderate overlapping COVID-19 wave, the CDC warns that it expects similar impacts and hospitalizations placing a severe strain on the healthcare system. A truly global concern, The World Health Organization estimates that nearly 7 million people have died from COVID-19 worldwide since the 2020 pandemic. It also estimates the impact of seasonal flu, killing approximately 290,000 to 650,000 people per year, while RSV may be responsible for 29,000 deaths per year.

自 COVID-19 疫情以來,這三種病毒感染的季節性感染率有所增加,而且 CDC 重點介紹去年 2022-2023 年的情況 “三聯疫情”,每週住院率超過每10萬人中有20人住院。如果本季出現嚴重的流感和呼吸道合胞病毒,以及適度重疊的 COVID-19 浪潮,疾病預防控制中心警告說,預計類似的影響和住院將給醫療系統帶來嚴重壓力。這是一個真正的全球性問題, 世界衛生組織估計 自 2020 年疫情以來,全球已有近 700 萬人死於 COVID-19。它還估計了季節性流感的影響,每年造成約29萬至65萬人死亡,而呼吸道合胞病毒每年可能造成29,000人死亡。

About Coeptis Therapeutics Holdings, Inc.

關於 Coeptis Therapeutics Holdings

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 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/.

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

關於前瞻性陳述的警示說明

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.

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:

聯繫人:

Coeptis Therapeutics, Inc.
Andy Galy, Sr. VP of Communications
andy.galy@coeptistx.com

Coeptis Therapeutics, Inc
Andy Galy,高級傳播副總裁
andy.galy@coeptistx.com

Media
David Schemelia
dschemelia@tiberend.com

媒體
大衛·謝梅利亞
dschemelia@tiberend.com

SOURCE Coeptis Therapeutics, Inc.

來源 Coeptis Therapeutics, Inc.

譯文內容由第三人軟體翻譯。


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