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Calidi Biotherapeutics Presents Data Supporting RTNova Systemic Technology to Target Metastatic Lung Cancer

Calidi Biotherapeutics Presents Data Supporting RTNova Systemic Technology to Target Metastatic Lung Cancer

Calidi生物治療公司展示了支持RTNova全身科技以靶向轉移性肺癌的數據
GlobeNewswire ·  11/18 21:00

SAN DIEGO, Nov. 18, 2024 (GLOBE NEWSWIRE) -- Calidi Biotherapeutics Inc. (NYSE American: CLDI) ("Calidi"), a clinical-stage biotechnology company developing a new generation of targeted antitumor virotherapies, presented data at the International Oncolytic Virotherapy Conference (IOVC) and the Society for Immunotherapy of Cancer (SITC) Annual Meeting to support the targeted capabilities of its proprietary RTNova systemic enveloped virotherapy technology. This data supports the potential use of RTNova to target every metastatic site in multiple oncology indications including metastatic lung cancer.

聖地亞哥,2024年11月18日(環球新聞社) - Calidi生物製藥公司(美國紐約證券交易所:CLDI)("Calidi"),一家處於臨床階段的生物技術公司,致力於開發新一代針對靶向抗腫瘤病毒療法,已在國際潰瘍病毒療法大會(IOVC)和癌症免疫療法協會(SITC)年會上展示了數據,以支持其專有RTNova系統封裝病毒療法技術的靶向能力。這些數據支持RTNova潛在用於針對包括轉移性肺癌在內的多個腫瘤適應症的每個轉移部位。

RTNova is uniquely designed to overcome key challenges in systemic virotherapy, including rapid immune clearance and limited therapeutic targeting. By incorporating enveloped technology into its tumor-selective vaccinia virus platform, RTNova now has the potential to target multiple metastatic tumor sites, killing and transforming, not one, but potentially all tumor microenvironments in the body. Calidi's enveloped virotherapies demonstrated robust therapeutic potential as a monotherapy and as a viral vector, allowing future expansion of functionality to support delivery of therapeutic gene or medicine payloads into all tumor sites.

RTNova獨特地設計用以克服系統性病毒治療中的關鍵挑戰,包括快速的免疫清除和有限的治療靶向。通過將包膜技術融入其腫瘤選擇性痘病毒平台,RTNova現在有潛力針對多個轉移性腫瘤部位,殺死並改變體內,可能不僅僅是一個,而是所有腫瘤微環境。Calidi的包膜病毒治療顯示出作爲單一療法和病毒載體的強大治療潛力,使未來功能擴展能夠支持將治療基因或藥物負載傳遞到所有腫瘤部位。

"New data presented at IOVC and SITC demonstrated the robust therapeutic potential of our RTNova technology in an advanced lung metastasis model," said Dr. Santidrian, Chief Scientific Officer of Calidi Biotherapeutics. "These findings represent a significant advancement in developing systemic antitumor virotherapy for advanced disease stages, which remains a leading cause of death in cancer patients. Additionally, the data reveals that once the virus reaches the tumors or metastases, it successfully kills and transforms tumor microenvironments and can additionally induce expression of engineered payloads in the tumor cells. We believe RTNova has the potential to transform how we address previously untreatable metastatic diseases."

「在IOVC和海豐國際上展示的新數據表明我們的RTNova技術在先進的肺轉移模型中具有強大的治療潛力,」Calidi生物治療公司的首席科學官Santidrian博士說。「這些發現代表了在先進疾病階段開發系統性抗腫瘤病毒治療的重大進展,該階段仍然是癌症患者死亡的主要原因。此外,數據表明一旦病毒到達腫瘤或轉移部位,就能成功殺死並改變腫瘤微環境,並且可以進一步誘導腫瘤細胞中工程化負載的表達。我們相信RTNova有潛力改變我們處理以前無法治療的轉移性疾病的方式。」

Download the poster presentation from SITC here.

從海豐國際下載海報演示。

RTNova utilizes a novel, tumor-selective strain of vaccinia virus engineered to produce high levels of extracellular enveloped viruses (EEVs). These EEVs are designed to integrate human cell-derived proteins enabling the targeting of tumor sites while avoiding rapid clearance by the host immune system. This latest enhancement extends RTNova's utility, making it a versatile platform as a direct antitumor modality, and as a viral vector for customized delivery of cancer treatments. This data will also support the advancement of potential collaborative relationships with pharma partners.

RTNova利用了一種新型的腫瘤選擇性牛痘病毒菌株,該病毒經過工程處理,能夠產生高水平的細胞外包膜病毒(EEVs)。這些EEVs被設計爲整合人類細胞衍生的蛋白質,能夠針對腫瘤部位,同時避免被宿主免疫系統迅速清除。這一最新增強功能擴展了RTNova的實用性,使其成爲一種多用途平台,既可以作爲直接的抗腫瘤方式,也可以作爲定製癌症治療的病毒載體。這些數據還將支持與製藥合作伙伴的潛在合作關係的推進。

Calidi Biotherapeutics continues to advance its clinical-stage, off-the-shelf, virotherapies. With RTNova, the company is planning multi-modal systemic antitumor virotherapies that can disrupt tumor growth, reprogram the tumor immune microenvironment, and achieve durable therapeutic outcomes for a larger patient population.

Calidi生物治療公司繼續推進其臨床階段的現成病毒治療。藉助RTNova,該公司計劃進行多模式的系統性抗腫瘤病毒治療,能夠破壞腫瘤生長,重新編程腫瘤免疫微環境,併爲更大患者群體實現持久的治療效果。

About Calidi Biotherapeutics

關於Calidi生物治療公司

Calidi Biotherapeutics (NYSE American: CLDI) is a clinical-stage immuno-oncology company with proprietary technology designed to arm the immune system to fight cancer. Calidi's novel stem cell-based platforms are utilizing potent allogeneic stem cells capable of carrying payloads of oncolytic viruses for use in multiple oncology indications, including high-grade gliomas and solid tumors. Calidi's clinical stage off-the-shelf, universal cell-based delivery platforms are designed to protect, amplify, and potentiate oncolytic viruses leading to enhanced efficacy and improved patient safety. Calidi's preclinical off-the-shelf enveloped virotherapies are designed to target disseminated solid tumors. This dual approach can potentially treat, or even prevent, metastatic disease. Calidi Biotherapeutics is headquartered in San Diego, California. For more information, please visit .

Calidi Biotherapeutics (紐交所美國股票代碼:CLDI)是一家臨床階段的免疫腫瘤療法公司,擁有專有技術,旨在武裝免疫系統與癌症抗爭。Calidi的新型幹細胞技術正在利用能夠攜帶腫瘤溶瘤病毒有效荷載的異基因幹細胞在多個癌症適應症中得到應用,包括高級別膠質瘤和實體瘤。Calidi的臨床階段現成的、通用的基於細胞的遞送平台旨在保護、放大和激發腫瘤溶解病毒,從而提高功效並改善患者安全性。Calidi的常規實驗室製備的外膜包裹的病毒治療方案旨在瞄準擴散性實體瘤。這一雙重方法可以潛在地治療甚至預防轉移性疾病。Calidi Biotherapeutics總部位於加利福尼亞州聖地亞哥。欲了解更多信息,請訪問。

Forward-Looking Statements

前瞻性聲明

This press release may contain forward-looking statements for purposes of the "safe harbor" provisions under the United States Private Securities Litigation Reform Act of 1995. Terms such as "anticipates," "believe," "continue," "could," "estimate," "expect," "intends," "may," "might," "plan," "possible," "potential," "predicts," "project," "should," "towards," "would" as well as similar terms, are forward-looking in nature, but the absence of these words does not mean that a statement is not forward-looking. These forward-looking statements include, but are not limited to, statements concerning upcoming key milestones (including the reporting of interim clinical results and the dosing of patients), planned clinical trials, and statements relating to the safety and efficacy of Calidi's therapeutic candidates in development. Any forward-looking statements contained in this discussion are based on Calidi's current expectations and beliefs concerning future developments and their potential effects and are subject to multiple risks and uncertainties that could cause actual results to differ materially and adversely from those set forth or implied in such forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that Calidi is not able to raise sufficient capital to support its current and anticipated clinical trials, the risk that early results of clinical trials do not necessarily predict final results and that one or more of the clinical outcomes may materially change following more comprehensive review of the data, and as more patient data becomes available, the risk that Calidi may not receive FDA approval for some or all of its therapeutic candidates. Other risks and uncertainties are set forth in the section entitled "Risk Factors" and "Cautionary Note Regarding Forward-Looking Statements" in the Company's Registration Statements filed with the SEC on (i) Form S-4 filed on August 2, 2023 and the corresponding prospectus filed on August 4, 2023, and (ii) on Form S-1 filed on April 15, 2024, and the Company's periodic reports filed with the SEC on (i) Form 10-K filed on March 15, 2024, (ii) Form 10-Q filed on May 14, 2024, (iii) Form 10-Q filed on August 13, 2024 and (iv) Form 10-Q filed on November 12, 2024. These reports may be amended or supplemented by other reports we file with the SEC from time to time.

本新聞稿可能包含根據1995年美國私人證券訴訟改革法的「安全港」條款的前瞻性陳述。諸如「預計」、「相信」、「繼續」、「可能」、「估計」、「期望」、「打算」、「可能」、「也許」、「計劃」、「可能的」、「潛在的」、「預測」、「項目」、「應該」、「朝向」、「會」等類似術語具有前瞻性,但缺乏這些詞並不意味着某項陳述不是前瞻性的。這些前瞻性陳述包括但不限於有關即將到來的關鍵里程碑(包括中期臨床結果的報告和患者的給藥)、計劃的臨床試驗,以及與Calidi正在開發的治療候選者的安全性和有效性相關的陳述。此討論中包含的任何前瞻性陳述均基於Calidi對未來發展的當前預期和信念及其潛在影響,並受到多種風險和不確定因素的影響,這些風險和不確定性可能導致實際結果與這些前瞻性陳述中所列或暗示的結果顯著不同。此外,這些風險和不確定性包括但不限於,Calidi未能籌集足夠資金以支持其當前和預期的臨床試驗的風險,臨床試驗的早期結果未必預測最終結果的風險,以及在更全面審查數據後,一個或多個臨床結果可能會顯著變化的風險,隨着患者數據的更多可用,Calidi可能無法獲得FDA對其某些或所有治療候選者的批准的風險。其他風險和不確定性在公司向SEC提交的註冊聲明中列出了「風險因素」和「關於前瞻性陳述的警告說明」部分,其中(i) 2023年8月2日提交的S-4表格及其相應的招股說明書在2023年8月4日提交,以及(ii) 2024年4月15日提交的S-1表格,及公司的定期報告在2024年3月15日提交的10-k表格,2024年5月14日提交的10-Q表格,2024年8月13日提交的10-Q表格以及2024年11月12日提交的10-Q表格。這些報告可能會被我們不時向SEC提交的其他報告修訂或補充。

For Investors:

對於投資者:

Dave Gentry, CEO
RedChip Companies, Inc.
1-407-644-4256
CLDI@redchip.com

首席執行官Dave Gentry
RedChip Companies, Inc.
1-407-644-4256
CLDI@redchip.com

Source: Calidi Biotherapeutics, Inc.

來源:Calidi生物技術公司,Inc。


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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