和铂医药与Cullinan Oncology就B7H4x4-1BB双特异性抗体签订授权及合作协议

EQS 新闻 via SEAPRWire.com / 2023-02-14 / 11:12 UTC+8 和铂医药与Cullinan Oncology就B7H4x4-1BB双特异性抗体签订授权及合作协议 HBM7008是一款针对B7H4x4-1BB的双特异性抗体,由和铂医药创新的免疫细胞衔接器HBICE®平台开发 和铂医药将获得2500万美元预付款和最高达6亿美元里程碑付款,以及最高近20%销售额百分比的分级特许使用权费 和铂医药保留美国地区以外HBM7008的所有权利,以此为前提,Cullinan Oncology亦有权在欧盟或澳大利亚进行人体临床研究,并与和铂医药共享相关临床资料 和铂医药(股票代码:02142.HK)今日宣布与Cullinan Oncology, Inc.(纳斯达克:CGEM)签订授权及合作协议,授予Cullinan Oncology在美国(包括哥伦比亚特区和波多黎各)开发及商业化HBM7008(Cullinan Oncology产品代号为CLN-418)的独家许可权。HBM7008是一款针对B7H4x4-1BB的双特异性抗体,由和铂医药创新的免疫细胞衔接器HBICE®平台开发,目前正处于I期临床开发阶段。 根据协议,和铂医药将获得2500万美元预付款和最高达6亿美元里程碑付款,以及最高近20%销售额百分比的分级特许使用权费。Cullinan Oncology将承担在美国地区开发及商业化HBM7008的所有费用,和铂医药保留美国地区以外HBM7008的所有权利。此外,Cullinan Oncology亦有权在欧盟或澳大利亚进行人体临床研究(前提为和铂医药将保留HBM7008的所有权利)并与和铂医药共享相关临床资料。 和铂医药创始人、董事长兼首席执行官及HBMAT董事会主席王劲松博士表示:“此次合作是全球领先的合作伙伴对我们的技术平台和创新能力的又一次认可,也是和铂医药向这一潜在全球首创肿瘤免疫疗法迈出的坚实脚步。得益于其独特的肿瘤表达特异性和免疫调控活性,HBM7008表现出强大的抗肿瘤疗效,我们相信Cullinan Oncology是进一步开发HBM7008的最佳合作伙伴,他们拥有专业的临床开发团队、强大的肿瘤药物开发能力以及配套的设备资源。我们期待与Cullinan Oncology紧密合作将这个具有巨大潜力的创新产品全速推进。” Cullinan Oncology 首席执行官Nadim Ahmed先生表示:“我们很高兴将HBM7008(CLN-418)这款潜在全球首创且进入临床阶段的双特异性抗体引入Cullinan Oncology多元化的产品管线。B7H4是一种肿瘤相关抗原,在多种癌症中高表达,与PD-L1的表达重叠度极小,我们相信B7H4x4-1BB是针对B7H4的最佳通路之一。HBM7008的引进是Cullinan Oncology战略布局的一部分,将充分发挥我们在双特异性方面的专长,巩固我们在针对实体瘤的双特异性抗体开发领域的地位。和铂医药拥有丰富的抗体疗法创新能力并具备广泛的全球合作网络,我们期待与其共同推进CLN-418/HBM7008的临床开发工作,从而最大化激发该产品的潜力与价值。” 关于HBM7008 HBM7008是一种针对肿瘤相关抗原B7H4x4-1BB的双特异性抗体,由于其高度依赖以肿瘤相关抗原为介导,与T细胞活化进行交叉链接,因此在T细胞共刺激及抑制肿瘤生长方面的功效显著,同时提高安全性。HBM7008基于和铂医药创新的HBICE®平台开发的全人源双特异性抗体,也是目前全球针对这两个靶点的唯一双特异性抗体。其独特的肿瘤表达特异性和免疫调控活性,有望在PD-L1阴性或对PD-1/PD-L1免疫治疗药物具耐药性的患者中,产生更好的疗效。凭借其新型生物学作用机制及双抗设计,有望避免4-1BB可能引发的肝毒性风险。 关于和铂医药 和铂医药(股票代码:02142.HK)是一家专注于肿瘤及免疫性疾病领域创新药研发及商业化的全球化生物制药企业。公司通过自主研发、联合开发及多元化的合作模式快速拓展创新药研发管线。 和铂自有的抗体技术平台Harbour Mice®可生成双重、双轻链(H2L2)和仅重链(HCAb)形式的全人源单克隆抗体。基于HCAb抗体平台开发的免疫细胞衔接器(HBICE®)能够实现传统药物联合疗法无法达到的抗肿瘤疗效。Harbour Mice®,HBICE®与单B细胞克隆筛选平台共同组成了和铂的下一代创新治疗性抗体研发引擎。 更多资讯,请访问 www.harbourbiomed.com 关于CULLINAN ONCOLOGY, INC Cullinan Oncology, Inc.(纳斯达克:CGEM)是一家生物制药公司,致力于为癌症患者创造新的护理标准。其无国界地开展创新,寻找最具前景的可用于临床的癌症疗法,无论是通过自身的发现努力或通过与学术和行业伙伴的特别合作。基于对免疫肿瘤学和癌症转化医学的深刻理解,其利用在小分子和生物制剂方面的科学优势,创造出与众不同的想法,确定独特的目标,并选择最佳方式来开发各种癌症适应症的转型疗法。在新型研究模式的推动下,其突破了从候选药物选择到癌症治疗的传统界限,应用严格的早期实验,只将最具前景的研究成果快速推向临床,最终实现商业化。因此,其多元化的管线是以激活免疫系统或抑制各种模式的关键致癌因素的研究成果策略性地构建而成,每项研究成果均有可能成为同类产品中最佳的或第一产品。 其员工拥有深厚的科学专业知识,寻求开放式创新,并发挥创造力,加紧研发工作,以实现为癌症患者带来新的治疗方案的承诺。 文件: 和铂医药与Cullinan Oncology就B7H4x4-1BB双特异性抗体签订授权及合作协议 2023-02-14 此财经新闻稿由EQS Group via SEAPRWire.com转载。本公告内容由发行人全权负责。原文链接: http://www.todayir.com/sc/index.php
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Novotech at ESMO Congress 2022 – New Data Shows 100% Oncology Trials Growth in APAC ACN Newswire

Novotech at ESMO Congress 2022 – New Data Shows 100% Oncology Trials Growth in APAC

SYDNEY, Sep 5, 2022 - (ACN Newswire via SEAPRWire.com) - Novotech, the leading Asia Pacific biotech specialist CRO, will attend ESMO Congress 2022 with new data showing Asia Pacific has seen a 100% growth in oncology trials during 2017 to 2021 and contributes to more than a third of the global clinical development of immune-oncology drugs.Novotech has experienced CRO operations across APAC and the US offering a unique and unparalleled suite of services for early to late phase biotech clinical research.The clinical data compiled by GlobalData for Novoteoch also found that: "By the end of 2021 40% of active immuno-oncology clinical trials involved at least one location in the Asia-Pacific region, with majority of trials conducted in China, followed by Australia, South Korea, Japan and Taiwan. In the APAC region, the proportion of oncology trials doubled during 2017-2021. In China, the growth in oncology trials was associated with a significant increase in cancer incidence, development of innovative products by domestic companies, focus on immune-oncology, and leadership in cell therapy."Download the Reports Here:IMMUNO-ONCOLOGY - ASIA PACIFIC - CLINICAL TRIAL LANDSCAPE https://novotech-cro.com/whitepapers/immuno-oncology-asia-pacific-clinical-trial-landscapeEVOLUTION OF CLINICAL TRIALS IN THE ASIA PACIFIC REGION COMPARED TO THE US AND THE EU5 https://novotech-cro.com/whitepapers/evolution-clinical-trials-asia-pacific-region-compared-us-and-eu5According to Yooni Kim, Vice President, Global Clinical Services Novotech: "Asia-Pacific offers a compelling solution for expedited clinical trials with its vast patient populations, less competitive clinical trial landscape, and world-class KOLs, in addition, regulatory reforms have accelerated approval processes. Novotech's service delivery model is tailored to the needs of biotech clients. Our local teams have exceptional site and investigator access, our project management approach emphasizes problem-solving, ownership and flexibility, and our investments in data and technology ensure clients have real-time access to trial performance."Novotech has recently been benchmarked as a top 10 CRO among the world's leading CROs, and has signed 45 Leading Site Partnership agreements over the last 3 years.About Novotech Novotech is the leading Asia-Pacific biotech specialist CRO. Novotech has integrated labs and phase I facilities and provides drug development consulting and clinical development services across all phases. It has been instrumental in the success of approximately 4,000 clinical trials across a broad range of therapeutic areas. Novotech is well-positioned to serve biopharma clients conducting clinical trials in Asia-Pacific and the US. For more information visit https://novotech-cro.com/contactMedia ContactDavid JamesE: communications@novotech-cro.comAU: +61 2 8218 2144 USA: +1 415 951 3228Asia: +65 3159 3427 Copyright 2022 ACN Newswire. All rights reserved. (via SEAPRWire)
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