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MiNK Therapeutics and Autonomous Therapeutics Announce Collaboration to Develop Novel Therapies Targeting Metastatic Tumors

MiNK Therapeutics and Autonomous Therapeutics Announce Collaboration to Develop Novel Therapies Targeting Metastatic Tumors

MiNk Therapeutics和Autonomous Therapeutics宣布合作,开发针对转移性肿瘤的新型疗法。
MiNK Therapeutics ·  10/08 00:00
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NEW YORK, Oct. 08, 2024 (GLOBE NEWSWIRE) -- MiNK Therapeutics (MiNK, NASDAQ: INKT) a clinical-stage company pioneering the development of allogeneic off-the-shelf, invariant natural killer T (iNKT) cell therapies and Autonomous Therapeutics, Inc. (Autonomous), a leader developing first-in-class, disease-activated RNA medicines, announced a research collaboration aimed at effectively targeting and treating metastatic tumors.

纽约,2024年10月8日(GLOBE NEWSWIRE)——MinK Therapeutics(MinK,纳斯达克股票代码:INKT)是一家开创异基因现成不变自然杀伤t(inKT)细胞疗法的临床阶段公司,以及开发同类首创疾病激活RNA药物的领导者Autonomoutics, Inc.(Autonomous)宣布了一项旨在有效靶向和治疗转移性肿瘤的研究合作。

This collaboration will leverage Autonomous' precision encrypted RNA (encRNA) technology and MiNK's innovative iNKT cell therapies, MiNK-215 and agenT-797. The companies will evaluate these technologies in state-of-the-art metastatic solid tumor models. The goal is to develop novel therapies that effectively target metastatic cancer cells in patients while avoiding healthy cells—a challenge that existing cancer medicines have not been able to overcome. Based on the results, the companies plan to launch a Phase 1 clinical trial in patients with treatment-refractory metastatic solid tumors, including microsatellite stable (MSS) colorectal cancers.

此次合作将利用Autonomous的精密加密核糖核酸(encRNA)技术和MinK的创新inKT细胞疗法mink-215和agent-797。两家公司将在最先进的转移性实体瘤模型中评估这些技术。目标是开发新疗法,有效靶向患者体内的转移癌细胞,同时避免使用健康细胞,这是现有抗癌药物无法克服的挑战。根据研究结果,两家公司计划启动一项针对难治性转移性实体瘤(包括微卫星稳定(MSS)结直肠癌患者的1期临床试验。

"This collaboration underscores the unique potential of both native and engineered iNKT cells, allowing us to explore cutting-edge approaches that could significantly enhance clinical responses and deliver better outcomes for patients," said Dr. Jennifer Buell, President and Chief Executive Officer at MiNK. "MiNK-215 and agenT-797 are novel cell therapies designed to overcome the limitations of traditional immune checkpoint inhibitors. Recent preclinical models of MSS colorectal cancer with metastatic liver disease demonstrated that these iNKT cells have the potential to eliminate tumor cells effectively. By combining them with Autonomous Therapeutics' engineered RNA technology, we are confident that we can unlock even greater therapeutic possibilities and continue advancing our mission to transform the landscape of cell therapy."

MinK总裁兼首席执行官詹妮弗·比尔博士表示:“这种合作凸显了天然和工程化inKT细胞的独特潜力,使我们能够探索尖端方法,这些方法可以显著增强临床反应并为患者带来更好的疗效。”“mink-215和agent-797是旨在克服传统免疫检查点抑制剂局限性的新型细胞疗法。最近伴有转移性肝病的 MSS 结直肠癌的临床前模型表明,这些 inKT 细胞有可能有效消灭肿瘤细胞。通过将它们与Autonomous Therapeutics的工程RNA技术相结合,我们相信我们可以开启更大的治疗可能性,并继续推进我们改变细胞疗法格局的使命。”

Dr. Ariel Weinberger, Chief Executive Officer of Autonomous, added: "This exciting collaboration leverages the platform capabilities of our next-generation encrypted RNA technology and MiNK's unique allogeneic cell therapy platform. AT313 is a preclinical encRNA candidate developed at Autonomous to enable the precision targeting of solid tumors, via cancer-activated therapeutic protein translation. Our aim is to develop novel medicines that pinpoint tumor cells in patients—by sensing and targeting the aberrant molecular signatures that define cancer replication. This would enable us to eliminate cancer cells in patients while sparing healthy and immune cells. It would also eliminate dose-limiting toxicities common to existing oncology medicines while significantly enhancing therapeutic efficacy—to dramatically improve Stage IV patient outcomes."

Autonomous首席执行官Ariel Weinberger博士补充说:“这项激动人心的合作利用了我们下一代加密RNA技术的平台功能和MinK独特的异基因细胞疗法平台。AT313 是Autonomous开发的临床前encRNA候选药物,旨在通过癌症激活的治疗性蛋白质翻译来精确靶向实体瘤。我们的目标是通过感知和靶向定义癌症复制的异常分子特征,开发能够精确定位患者体内肿瘤细胞的新药物。这将使我们能够消灭患者体内的癌细胞,同时保留健康和免疫细胞。它还将消除现有肿瘤药物常见的剂量限制毒性,同时显著提高治疗效果,从而显著改善IV期患者的预后。”

About MiNK-215

关于 mink-215

MiNK-215 is an investigational, off-the-shelf cellular immunotherapy, specifically designed to target immune resistance mechanisms and promote a potent anti-cancer immune response. Engineered to express CAR targeting the Fibroblast Activating Protein (FAP) protein prevalent in stromal cells within the tumor microenvironment, MiNK-215 also integrates soluble IL-15 for enhanced persistence (Michelet X et al, SITC 2022; Shan K et al, AACR 2023; Dijk MV et al, CICON 2023). In preclinical models resistant to immune checkpoint inhibitors, MiNK-215 has demonstrated remarkable efficacy, not only in eliminating tumor cells and FAP+ immune-suppressive cells but also facilitating the infiltration and persistence of proinflammatory cytotoxic T cells crucial for effective tumor elimination.

Mink-215是一种研究性现成细胞免疫疗法,专门设计用于靶向免疫耐药机制并促进有效的抗癌免疫反应。mink-215 专为表达针对肿瘤微环境中基质细胞中普遍存在的成纤维细胞活化蛋白 (FAP) 蛋白的 CAR 而设计,还集成了可溶性 IL-15 以增强持久性(Michelet X 等人,SITC 2022;Shan k 等人,AACR 2023;Dijk MV 等人,CICON 2023)。在对免疫检查点抑制剂具有耐药性的临床前模型中,mink-215已显示出显著的功效,不仅在消灭肿瘤细胞和FAP+免疫抑制细胞方面,而且还能促进对有效消除肿瘤至关重要的促炎细胞毒性T细胞的浸润和持久性。

About agenT-797

关于 agent-797

AgenT-797 is an investigational, off-the-shelf immune cell therapy product by MiNK Therapeutics, possessing anti-viral and immune-modulating properties. In a Phase 1 trial involving 54 patients with heavily pre-treated solid tumors, agenT-797 appears to overcome resistance to immune checkpoint inhibitors, with durable disease stabilization in multiple solid tumors and a confirmed response in chemotherapy and anti-PD-1 refractory gastric cancer (Carneiro et al, 2024 Oncogene). agenT-797 is being evaluated in an investigator sponsored Phase 2 trial in 2L gastric cancer, led by Dr. Yelena Janjigian, Chief of GI Oncology at Memorial Sloan-Kettering Cancer Center and supported by Stand Up to Cancer.

Agent-797是MinK Therapeutics推出的研究性现成免疫细胞疗法产品,具有抗病毒和免疫调节特性。在一项涉及54名经过大量预处理的实体瘤患者的1期试验中,agent-797似乎克服了对免疫检查点抑制剂的耐药性,在多种实体瘤中具有持久的疾病稳定性,化疗和抗PD-1难治性胃癌的反应得到证实(Carneiro等人,2024 Oncogene)。agent-797正在由叶琳娜·詹吉安博士领导的研究人员赞助的2L胃癌2期试验中进行评估,纪念斯隆·凯特琳癌症中心消化道肿瘤学主任,由 Stand Up to Cancer 提供支持。

About MiNK Therapeutics

关于 MinK Therapeut

MiNK Therapeutics is a clinical-stage biopharmaceutical company pioneering the discovery, development, and commercialization of allogeneic invariant natural killer T (iNKT) cell therapies to treat cancer and other immune-mediated diseases. MiNK is advancing a pipeline of both native and next generation engineered iNKT programs, with a platform designed to facilitate scalable and reproducible manufacturing for off-the-shelf delivery. The company is headquartered in New York, NY. For more information, visit or @MiNK_iNKT. Information that may be important to investors will be routinely posted on our website and social media channels.

MinK Therapeutics 是一家临床阶段的生物制药公司,率先发现、开发和商业化用于治疗癌症和其他免疫介导疾病的异基因不变自然杀伤 t (inKT) 细胞疗法。MinK正在推进原生和下一代工程InKT程序的管道,其平台旨在促进可扩展和可重复的制造,以实现现成交付。该公司总部位于纽约州纽约。欲了解更多信息,请访问或 @MiNK_iNKt。可能对投资者很重要的信息将定期发布在我们的网站和社交媒体渠道上。

About Autonomous Therapeutics, Inc.

关于自主疗法公司

Autonomous Therapeutics is pioneering a new class of RNA medicines (encRNA) for difficult-to-treat indications in oncology and infectious disease. Autonomous has developed a proprietary pipeline of more than 10 encRNA candidates targeting indications from pandemic influenza to metastatic cancers. The company's encRNA pipeline includes next-generation immunotherapies such as AT313, a cancer-activated RNA prodrug designed to precisely eliminate solid tumor cells. Autonomous' partners and funders have included: the Defense Advanced Research Projects Agency (DARPA), the National Institutes of Health (NIH), the Office of the Secretary of Defense (OSD), Third Kind Venture Capital (3kVC), and BLUE KNIGHT, a joint initiative between the Biomedical Advanced Research and Development Authority (BARDA) and Johnson & Johnson Innovation – JLABS.

Autonomous Therapeutics正在开创一种新的RNA药物(encRNA),用于肿瘤学和传染病中难以治疗的适应症。Autonomous开发了一条包含10多种encRNA候选药物的专有产品线,靶向从大流行性流感到转移性癌症的适应症。该公司的encRNA产品线包括下一代免疫疗法,例如 AT313,这是一种旨在精确消灭实体瘤细胞的癌症活化RNA前药。Autonomous的合作伙伴和资助者包括:国防高级研究计划局(DARPA)、美国国立卫生研究院(NIH)、国防部长办公室(OSD)、第三类风险投资(3kVC)以及生物医学高级研究与发展局(BARDA)和强生创新联合发起的BLUE Knight——JLABS。

About encrypted RNA

关于加密 RNA

encRNA is a new class of RNA invented at Autonomous to enable the development of precision medicines against virtually any disease driven by aberrant nucleic acid expression or protein translation. Autonomous' encRNA therapeutics leverage the molecular signatures of a targeted disease as intracellular logic gates—to drive precision therapeutic protein translation in targeted cells. Each encRNA candidate is designed to differentiate between healthy and diseased cells across a patient and to translate therapeutic proteins solely in diseased cells. encRNA candidates are modular and can be programmed with multiple logic gates for potential patient-specific sensitivity and specificity. In proof-of-concept studies, Autonomous has demonstrated the preclinical safety and efficacy of encRNA candidates in animal models, with the potential to completely eradicate immunologically "cold" solid tumors via precision immunotherapy.

encRNA 是 Autonomous 发明的一类新型 RNA,旨在开发针对几乎任何由异常核酸表达或蛋白质翻译引起的疾病的精准药物。Autonomous的encRNA疗法利用靶向疾病的分子特征作为细胞内逻辑门户,推动靶向细胞中精确的治疗性蛋白质翻译。每个 encRNA 候选药物都旨在区分患者的健康细胞和患病细胞,并仅翻译患病细胞中的治疗蛋白。encRNA 候选药物是模块化的,可使用多个逻辑门进行编程,以提高潜在的患者特异性灵敏度和特异性。在概念验证研究中,Autonomous已经证明了动物模型中eNcRNA候选药物的临床前安全性和有效性,有可能通过精准免疫疗法彻底根除免疫学上的 “冷” 实体瘤。

Forward Looking Statements

前瞻性陈述

This press release contains forward-looking statements that are made pursuant to the safe harbor provisions of the federal securities laws, including statements regarding the therapeutic potential, anticipated benefit, plans and timelines of iNKT cells and encrypted RNA, as well as the collaboration between MiNK and Autonomous Therapeutics. These forward-looking statements are subject to risks and uncertainties that could cause actual results to differ materially. These forward-looking statements are subject to risks and uncertainties, including the factors described under the Risk Factors section of the most recent Form 10-K, Form 10-Q and the S-1 Registration Statement filed with the SEC. MiNK cautions investors not to place considerable reliance on the forward-looking statements contained in this release. These statements speak only as of the date of this press release, and MiNK and Autonomous undertake no obligation to update or revise the statements, other than to the extent required by law. All forward-looking statements are expressly qualified in their entirety by this cautionary statement.

本新闻稿包含根据联邦证券法安全港条款做出的前瞻性陈述,包括有关InKT细胞和加密RNA的治疗潜力、预期益处、计划和时间表以及MinK与Autonomous Therapeutics之间合作的声明。这些前瞻性陈述受风险和不确定性的影响,可能导致实际结果出现重大差异。这些前瞻性陈述受风险和不确定性的影响,包括向美国证券交易委员会提交的最新10-k表格、10-Q表格和S-1注册声明中 “风险因素” 部分中描述的因素。MinK提醒投资者不要过分依赖本新闻稿中包含的前瞻性陈述。这些声明仅代表截至本新闻稿发布之日,除法律要求外,MinK和Autonomous没有义务更新或修改这些声明。本警示性陈述对所有前瞻性陈述进行了明确的完整限定。

MiNK Investor Contact

minK 投资者联系方式

917-362-1370

917-362-1370

investor@minktherapeutics.com

investor@minktherapeutics.com

MiNK Media Contact

minK 媒体联系人

781-674-4428

781-674-4428

communications@minktherapeutics.com

communications@minktherapeutics.com


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Source: MiNK Therapeutics

来源:MinK Therapeutics

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