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To benchmark the utility of E06: A half-life extension, single-domain, shark antibody bio-tool, and progress it to a Phase 1 ready candidate clone

To benchmark the utility of E06: A half-life extension, single-domain, shark antibody bio-tool, and progress it to a Phase 1 ready candidate clone
对 E06 的实用性进行基准测试:一种半衰期延长、单域、鲨鱼抗体生物工具,并将其发展为第一阶段就绪的候选克隆
批准号:
BB/K010905/1
负责人:
Andrew Porter
金额:
$55.49万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2013
资助国家:
英国
项目状态:
已结题
起止时间:
2013 至 --

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中文摘要
翻译
从科学上讲,我们正在开发一种“生物工具”,它可以与一系列不同的治疗蛋白/多肽融合,将它们的血清半衰期从几个小时延长到几周,并有可能极大地提高它们的治疗效力。它的工作原理是搭乘血液中其他长寿蛋白质的便车。在商业上,我们的中期目标是在我们独特的单域鲨鱼抗体(VNAR)平台的基础上创建一家药物发现公司,该平台将在内部或与较大公司合作开发治疗剂。要实现这一点,满足科学里程碑是关键,特别是确认非免疫原性(人类免疫系统看不到,使用安全),并验证我们最先进的产品(E06 VNAR半寿命延长生物工具)。实现这一目标的进展还将为新公司的成立和股权融资提供一个平台,并将交付一项能够确保许可和合作收入的多种收入来源的资产。
英文摘要
Scientifically we are developing a "bio-tool" that could be fused to a range of different therapeutic proteins/peptides to extend their serum half-life from hours to weeks, with the potential of greatly increasing their therapeutic potency. It works by hitching a ride on other long-lived proteins in the blood. Commercially, our medium-term goal is to create a Drug Discovery company, based on our unique, single-domain shark antibody (VNAR) platform, which will develop therapeutic agents in-house or in partnership with larger companies. To achieve this, meeting of scientific milestones is key, and in particular confirming non-immunogenicity (not seen by the human immune system & safe for use), and validate the most advanced of our products (E06 VNAR half-life extension bio-tool). Progress towards this goal will also provide a platform for NewCo formation and equity raising, and will deliver an asset capable of securing multiple revenue streams of licensing and partnered income.
期刊论文(10)
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会议论文
DOI: 10.3389/fimmu.2017.01361
发表时间: 2017
期刊: Frontiers in immunology
影响因子: 7.3
作者: [Steven J, Müller MR, Carvalho MF, Ubah OC, Kovaleva M, Donohoe G, Baddeley T, Cornock D, Saunders K, Porter AJ, Barelle CJ]
通讯作者: Barelle CJ
In Vitro ELISA and Cell-Based Assays Confirm the Low Immunogenicity of VNAR Therapeutic Constructs in a Mouse Model of Human RA: An Encouraging Milestone to Further Clinical Drug Development.
体外 ELISA 和基于细胞的测定证实 VNAR 治疗结构在人类 RA 小鼠模型中的低免疫原性:进一步临床药物开发的一个令人鼓舞的里程碑。
DOI: 10.1155/2020/7283239
发表时间: 2020
期刊: Journal of immunology research
影响因子: 4.1
作者: [Ubah OC]
通讯作者: Ubah OC
DOI: 10.4161/19420862.2015.989032
发表时间: 2015
期刊: mAbs
影响因子: 5.3
作者: [Zielonka S, Empting M, Grzeschik J, Könning D, Barelle CJ, Kolmar H]
通讯作者: Kolmar H
DOI: 10.1155/2018/4089459
发表时间: 2018
期刊: Journal of immunology research
影响因子: 4.1
作者: [O'Dwyer R, Kovaleva M, Zhang J, Steven J, Cummins E, Luxenberg D, Darmanin-Sheehan A, Carvalho MF, Whitters M, Saunders K, Barelle CJ]
通讯作者: Barelle CJ
Cell cycle control of DNA double strand break repair and the role of Cdk
  • 批准号:
    BB/H003371/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $40.35万
  • 财政年份:
    2010
  • 负责人:
    Andrew Porter
  • 依托单位:
海外基金