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Lisata Therapeutics Wins 2024 BioTech Breakthrough Award for 'Specialized BioTherapeutics Company of the Year'

Lisata Therapeutics Wins 2024 BioTech Breakthrough Award for 'Specialized BioTherapeutics Company of the Year'

Lisata Therapeutics荣获2024年生物科技突破奖“年度专业生物治疗公司”
Lisata Therapeutics ·  11/19 00:00

Award recognizes Lisata's data-driven approach and innovative therapies designed to address the unmet medical needs of patients with advanced solid tumors

该奖项旨在表彰Lisata的数据驱动方法和创新疗法,旨在满足晚期实体瘤患者未得到满足的医疗需求

Annual BioTech Breakthrough Award is devoted to honoring excellence in life science and biotechnology solutions, services, and companies

年度生物技术突破奖致力于表彰在生命科学和生物技术解决方案、服务和公司方面的卓越表现

BASKING RIDGE, N.J., Nov. 19, 2024 (GLOBE NEWSWIRE) -- Lisata Therapeutics, Inc. (Nasdaq: LSTA) (or the "Company"), a clinical-stage pharmaceutical company developing innovative therapies for the treatment of advanced solid tumors and other serious diseases, today announced that it has been selected as 'Specialized BioTherapeutics Company of the Year' in the fourth annual BioTech Breakthrough Awards program conducted by BioTech Breakthrough, a leading independent market intelligence organization that evaluates and recognizes standout life sciences and biotechnology companies, products, and services around the globe.

新泽西州巴斯金里奇,2024年11月19日(GLOBE NEWSWIRE)——开发治疗晚期实体瘤和其他严重疾病创新疗法的临床阶段制药公司Lisata Therapeutics, Inc.(纳斯达克股票代码:LSTA)(或 “公司”)今天宣布,在由该组织举办的第四届年度生物技术突破奖计划中被选为 “年度专业生物治疗公司” 生物技术突破,一家领先的独立市场情报组织,负责评估和表彰全球杰出的生命科学和生物技术公司、产品和服务。

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Lisata is recognized for its unique therapeutic approach and streamlined clinical development plans, designed to address the unmet medical needs of patients with advanced solid tumors. Through its proprietary CendR Platform technology, which enables more effective tumor-targeted and tissue-penetrating delivery of anti-cancer drugs by activating the CendR transport mechanism, Lisata aims to improve the efficacy of existing standards-of-care and emerging anti-cancer therapies, including cytotoxics, immunotherapies, and RNA-based treatments.

Lisata因其独特的治疗方法和简化的临床开发计划而获得认可,这些计划旨在满足晚期实体瘤患者未得到满足的医疗需求。Lisata旨在通过其专有的CendR平台技术来提高现有护理标准和新兴抗癌疗法(包括细胞毒素、免疫疗法和基于RNA的治疗)的疗效,该技术通过激活cENdR转运机制来实现更有效的肿瘤靶向和组织穿透性输送。

By modifying the tumor microenvironment ("TME"), the Company's investigational product candidate, certepetide, reduces the immunosuppressive nature of the TME, recruits cytotoxic T cells to the tumor, and simultaneously inhibits the metastatic cascade. Certepetide has shown favorable results in enhancing the effectiveness of chemotherapy for pancreatic cancer and has received Fast Track and Orphan Drug designations from the U.S. Food and Drug Administration ("FDA") for the treatment of pancreatic ductal adenocarcinoma ("PDAC"), along with Orphan Drug designation from the FDA for cholangiocarcinoma ("CCA"), and glioblastoma multiforme ("GBM"). Lisata has also received a Rare Pediatric Disease designation for certepetide in osteosarcoma.

通过改变肿瘤微环境(“TME”),该公司的候选研究产品certepide降低了TME的免疫抑制性质,向肿瘤招募了细胞毒性T细胞,同时抑制了级联转移。Certepetide在提高胰腺癌化疗的有效性方面显示出良好的效果,并已获得美国食品药品监督管理局(“FDA”)的用于治疗胰腺导管腺癌(“PDAC”)的快速通道和孤儿药认证,以及美国食品药品管理局对胆管癌(“CCA”)和多形胶质母细胞瘤(“胶质母细胞瘤”)的孤儿药认证(“CCA”)GBM”)。Lisata还因治疗骨肉瘤而获得了 “罕见儿科疾病” 称号。

"Winning the 'Specialized BioTherapeutics Company of the Year' award is a testament to Lisata's commitment to advancing the research and development of therapies to provide better outcomes for patients with solid tumors," said David J. Mazzo, Ph.D., President and Chief Executive Officer of Lisata. "Thank you to BioTech Breakthrough for this acknowledgment of the entire Lisata team and our partners. We will continue our focus on advancing our robust portfolio with the goal of bringing life-changing treatments to patients as quickly as possible."

Lisata总裁兼首席执行官戴维·马佐博士表示:“获得'年度专业生物治疗公司'奖证明了Lisata致力于推进疗法的研发,为实体瘤患者提供更好的疗效。”“感谢 Biotech Breakthrough 对整个 Lisata 团队和我们的合作伙伴的认可。我们将继续专注于推进我们强大的产品组合,目标是尽快为患者提供改变生活的治疗方法。”

"Lisata is continuing to transform patient lives through the discovery, development, and commercialization of innovative therapies for advanced solid tumors. The Company's novel product candidate, certepetide, is currently being evaluated in several ongoing clinical trials for the treatment of advanced solid tumors, including PDAC, CCA, GBM, colon cancer, appendiceal cancer, and melanoma," said Bryan Vaughn, Managing Director of BioTech Breakthrough. "Lisata is also exploring certepetide's potential in the treatment of non-oncologic applications such as endometriosis. This further demonstrates their commitment to developing cutting-edge therapies that address critical unmet medical needs, making them our well-deserved winner of the 'Specialized BioTherapeutics Company of the Year.'"

“Lisata通过发现、开发和商业化晚期实体瘤创新疗法,继续改变患者的生活。Biotech Breakthrough董事总经理Bryan Vaughn说,该公司的新型候选产品certepedite目前正在几项正在进行的临床试验中接受评估,用于治疗晚期实体瘤,包括PDAC、CCA、gBM、结肠癌、阑尾癌和黑色素瘤。“Lisata还在探索certepedite在治疗子宫内膜异位症等非肿瘤学应用中的潜力。这进一步表明他们致力于开发尖端疗法,以满足未满足的关键医疗需求,使他们成为我们当之无愧的'年度专业生物治疗公司'的赢家。”

The mission of the annual BioTech Breakthrough Awards program is to conduct the industry's most comprehensive analysis and evaluation of the world's top companies, solutions, and products in the life sciences and biotechnology markets today. This year's program attracted thousands of nominations from over 14 different countries throughout the world, serving as a global recognition platform that encourages bold ideas and solutions that will shape the future of biotechnology.

年度生物技术突破奖计划的使命是对当今生命科学和生物技术市场的世界顶级公司、解决方案和产品进行业内最全面的分析和评估。今年的项目吸引了来自全球超过14个不同国家的数千名提名,是一个全球认可平台,鼓励塑造生物技术未来的大胆想法和解决方案。

About Certepetide

关于 Certepetide

Certepetide is an investigational drug designed to selectively activate the C-end rule active transport mechanism in a tumor specific manner, resulting in systemically co-administered anti-cancer agents more efficiently penetrating and accumulating in the tumor. Additionally, certepetide has been shown to modify the tumor microenvironment, diminishing its immunosuppressive nature and inhibiting the metastatic cascade. Lisata and its collaborators have amassed significant non-clinical data demonstrating enhanced delivery of various existing and emerging anti-cancer therapies, including chemotherapies, immunotherapies and RNA-based therapeutics. To date, certepetide has also demonstrated favorable safety, tolerability, and clinical activity in completed and ongoing clinical trials designed to demonstrate its ability to enhance the effectiveness of standard-of-care chemotherapy for pancreatic cancer as well as the combination of chemotherapy and immunotherapy in a variety of solid tumors. Certepetide has been awarded Fast Track designation (U.S.) and Orphan Drug Designation for pancreatic cancer (U.S. and E.U.), as well as Orphan Drug Designation for glioma, osteosarcoma, and cholangiocarcinoma (U.S.). Additionally, certepetide has received Rare Pediatric Disease Designation for osteosarcoma (U.S.).

Certepetide是一种在研药物,旨在以肿瘤特异性方式选择性激活C端规则的主动转运机制,从而使全身共用的抗癌药物更有效地穿透和积聚在肿瘤中。此外,certepetide已被证明可以改变肿瘤微环境,降低其免疫抑制性质并抑制转移级联。Lisata及其合作者已经积累了大量的非临床数据,表明各种现有和新兴的抗癌疗法(包括化疗、免疫疗法和基于RNA的疗法)的交付得到了加强。迄今为止,certepetide在已完成和正在进行的临床试验中也显示出良好的安全性、耐受性和临床活性,这些试验旨在证明其能够增强胰腺癌标准护理化疗的有效性,以及对各种实体瘤进行化疗和免疫疗法的组合。Certepetide已被授予胰腺癌快速通道称号(美国)和孤儿药称号(美国和欧盟),以及神经胶质瘤、骨肉瘤和胆管癌的孤儿药称号(美国)。此外,certepetide已获得骨肉瘤罕见儿科疾病认定(美国)。

About Lisata Therapeutics

关于 Lisata Therapeu

Lisata Therapeutics is a clinical-stage pharmaceutical company dedicated to the discovery, development and commercialization of innovative therapies for the treatment of advanced solid tumors and other major diseases. Lisata's internalizing RGD, or Arginylglycylaspartic acid, (iRGD) cyclic peptide product candidate, certepetide, is an investigational drug designed to activate a novel uptake pathway that allows co-administered or tethered anti-cancer drugs to selectively target and penetrate solid tumors more effectively. Lisata has already established noteworthy commercial and R&D partnerships based on its CendR Platform technology. The Company expects to announce numerous milestones over the next 1.5 years and believes that its projected capital will fund operations into early 2026, encompassing anticipated data milestones from its ongoing and planned clinical trials. Learn more about certepetide's mechanism of action in our short film. For more information on the Company, please visit .

Lisata Therapeutics 是 处于临床阶段的制药公司 致力于发现、开发和商业化治疗晚期实体瘤和其他主要疾病的创新疗法。Lisata的内化RGD或精氨酰甘氨酸(iRGD)的循环肽候选产品赛替肽是一种在研药物,旨在激活一种新的摄取途径,该途径允许共同给药或联用抗癌药物更有效地选择性靶向和穿透实体瘤。Lisata已经在其基础上建立了值得注意的商业和研发合作伙伴关系 CendR 平台技术。该公司预计将在未来1.5年内宣布众多里程碑,并相信其预计资本将为2026年初的运营提供资金,其中包括正在进行和计划中的临床试验的预期数据里程碑。在我们的短片中详细了解赛替肽的作用机制。有关该公司的更多信息,请访问 .

About BioTech Breakthrough

关于《生物技术突破》

Part of Tech Breakthrough, a leading market intelligence and recognition platform for global technology innovation and leadership, the BioTech Breakthrough Awards program is devoted to honoring excellence in life science and biotechnology solutions, services and companies. The BioTech Breakthrough Awards provide public recognition for the achievements of biotechnology companies and products in categories including BioPharma, Genomics, Therapeutics, Immunology, Food Science and BioAgriculture, and more. For more information visit BioTechBreakthroughAwards.com

的一部分 科技突破作为全球技术创新和领导力的领先市场情报和表彰平台,生物技术突破奖计划致力于表彰生命科学和生物技术解决方案、服务和公司的卓越表现。生物技术突破奖旨在公开表彰生物技术公司和产品在生物制药、基因组学、治疗学、免疫学、食品科学和生物农业等领域取得的成就。欲了解更多信息,请访问 生物技术突破Awards.com

Tech Breakthrough LLC does not endorse any vendor, product or service depicted in our recognition programs, and does not advise technology users to select only those vendors with award designations. Tech Breakthrough LLC recognition consists of the opinions of the Tech Breakthrough LLC organization and should not be construed as statements of fact. Tech Breakthrough LLC disclaims all warranties, expressed or implied, with respect to this recognition program, including any warranties of merchantability or fitness for a particular purpose.

Tech Breakthrough LLC 不认可我们的表彰计划中描述的任何供应商、产品或服务,也不建议技术用户只选择具有奖项名称的供应商。Tech Breakthrough LLC的认可包括Tech Breakthrough LLC组织的观点,不应被解释为事实陈述。Tech Breakthrough LLC对本认可计划不作任何明示或暗示的担保,包括对适销性或特定用途适用性的任何担保。

Forward-Looking Statements

前瞻性陈述

This communication contains "forward-looking statements" that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical facts, included in this communication regarding the Company's clinical development programs are forward-looking statements. In addition, when or if used in this communication, the words "may," "could," "should," "anticipate," "believe," "estimate," "expect," "intend," "plan," "predict" and similar expressions and their variants, as they relate to Lisata or its management, may identify forward-looking statements. Examples of forward-looking statements include, but are not limited to, the potential efficacy of certepetide as a treatment for patients with melanoma and other solid tumors; statements relating to Lisata's continued listing on the Nasdaq Capital Market; expectations regarding the capitalization, resources and ownership structure of Lisata; the approach Lisata is taking to discover and develop novel therapeutics; the adequacy of Lisata's capital to support its future operations and its ability to successfully initiate and complete clinical trials; and the difficulty in predicting the time and cost of development of Lisata's product candidates. Actual results could differ materially from those contained in any forward-looking statement as a result of various factors, including, without limitation: results observed from a single patient case study are not necessarily indicative of final results and one or more of the clinical outcomes may materially change following more comprehensive reviews of the data and as more patient data becomes available, including the risk that unconfirmed responses may not ultimately result in confirmed responses to treatment after follow-up evaluations; the risk that product candidates that appeared promising in early research and clinical trials do not demonstrate safety and/or efficacy in larger-scale or later clinical trials; the safety and efficacy of Lisata's product candidates, decisions of regulatory authorities and the timing thereof, the duration and impact of regulatory delays in Lisata's clinical programs, Lisata's ability to finance its operations, the likelihood and timing of the receipt of future milestone and licensing fees, the future success of Lisata's scientific studies, Lisata's ability to successfully develop and commercialize drug candidates, the timing for starting and completing clinical trials, rapid technological change in Lisata's markets, the ability of Lisata to protect its intellectual property rights; and legislative, regulatory, political and economic developments. The foregoing review of important factors that could cause actual events to differ from expectations should not be construed as exhaustive and should be read in conjunction with statements that are included herein and elsewhere, including the risk factors included in Lisata's Annual Report on Form 10-K filed with the SEC on February 29, 2024, and in other documents filed by Lisata with the Securities and Exchange Commission. Except as required by applicable law, Lisata undertakes no obligation to revise or update any forward-looking statement, or to make any other forward-looking statements, whether as a result of new information, future events or otherwise.

本通信包含 “前瞻性陈述”,这些陈述涉及重大风险和不确定性,以实现1995年《私人证券诉讼改革法》提供的安全港。除历史事实陈述外,本通讯中包含的有关公司临床开发计划的所有陈述均为前瞻性陈述。此外,当或如果在本通信中使用 “可能”、“可以”、“应该”、“预测”、“相信”、“估计”、“期望”、“打算”、“计划”、“预测” 等词语以及与Lisata或其管理层相关的类似表述及其变体,可能代表前瞻性陈述。前瞻性陈述的例子包括但不限于:certepetide治疗黑色素瘤和其他实体瘤患者的潜在疗效;与Lisata继续在纳斯达克资本市场上市有关的陈述;对Lisata资本、资源和所有权结构的预期;Lisata为发现和开发新疗法所采取的方法;Lisata支持其未来运营的足够资金及其成功启动和完成的能力临床试验;以及难以预测Lisata候选产品的开发时间和成本。由于各种因素,实际结果可能与任何前瞻性陈述中包含的结果存在重大差异,包括但不限于:从单个患者案例研究中观察到的结果不一定代表最终结果,在对数据进行更全面的审查之后,随着更多患者数据的出现,包括未经证实的反应在后续评估后可能最终无法导致对治疗产生确认反应的风险;该产品的风险在早期研究和临床试验中表现出前景的候选药物在更大规模或以后的临床试验中并未表现出安全性和/或有效性;Lisata候选产品的安全性和有效性、监管机构的决定及其时间、Lisata临床项目监管延误的持续时间和影响、Lisata为其运营融资的能力、收到未来里程碑和许可费的可能性和时机、Lisata科学研究的未来成功、Lisata科学研究的未来成功、Lisata的未来成功成功开发的能力和候选药物的商业化、开始和完成临床试验的时机、Lisata市场的快速技术变革、Lisata保护其知识产权的能力;以及立法、监管、政治和经济发展。上述对可能导致实际事件与预期不同的重要因素的审查不应解释为详尽无遗,应与本文和其他地方的陈述一起阅读,包括Lisata于2024年2月29日向美国证券交易委员会提交的10-k表年度报告以及Lisata向美国证券交易委员会提交的其他文件中包含的风险因素。除非适用法律要求,否则Lisata没有义务修改或更新任何前瞻性陈述,也没有义务做出任何其他前瞻性陈述,无论是由于新信息、未来事件还是其他原因。

Lisata Therapeutics Contact:

Lisata 疗法联系人:

Investors:
Lisata Therapeutics
John Menditto
Vice President, Investor Relations and Corporate Communications
Phone: 908-842-0084
Email: jmenditto@lisata.com

投资者:
Lisata 疗法
约翰·门迪托
投资者关系和企业传播副总裁
电话:908-842-0084
电子邮件:jmenditto@lisata.com

Media:
ICR Healthcare
Elizabeth Coleman
Senior Associate
Phone: 203-682-4783
Email: elizabeth.coleman@westwicke.com

媒体:
ICR 医疗保健
伊丽莎白·科尔曼
高级助理
电话:203-682-4783
电子邮件:elizabeth.coleman@westwicke.com

A photo accompanying this announcement is available at

本公告附带的照片可在以下网址获得


声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息
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