PO.ET02.01 · 实验与分子治疗

通过先进的WuXiDARx偶联技术助力新一代ADC和XDC的研发

Empowering development of next generation ADCs & XDCs through advanced WuXiDARx conjugation technologies

海报缩略图:通过先进的WuXiDARx偶联技术助力新一代ADC和XDC的研发
编号 1688 展板 17 时间 4/20 09:00–12:00 区域 Section 12 主讲 Cindy Cheng, PhD
分会场 Antibody-Drug Conjugates and Linker Engineering 1
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作者与单位 Authors & Affiliations

Qirui Fan, Hu Chen, Jingjie Huang, Lin Zhang, Zekun Wang, Ding Wei, Guoguang Wei, Yanjie Zhao, Laisen Wang, Cindy Cheng, Marie Zhu

Discovery and Development, WuXi XDC, Shanghai, China

摘要 Abstract

中文摘要
背景:抗体偶联药物(ADC)和各类生物偶联物(XDC)在过去十年中受到越来越多的关注。这些新型载荷和载荷组合需要先进的偶联技术才能充分发挥其治疗潜力。传统上,链间半胱氨酸偶联是临床验证最充分的偶联技术。然而,此类方法有两大缺陷:(1)随机偶联导致的异质性(DAR8除外);(2)由于马来酰亚胺逆Michael加成反应导致循环过程中的不稳定性。 解决方案:为满足这些需求,药明合联通过内部研发和外部合作构建了一个平台。该平台包括两部分:(1)WuXiDARx™偶联技术。WuXiDARx™在链间半胱氨酸位点进行偶联,这是临床验证最充分的位点,18种上市ADC中有13种是通过半胱氨酸偶联开发的。该技术具有以下特点:•灵活的DAR选择(WuXiDAR1™、WuXiDAR2™、WuXiDAR4™、WuXiDAR6™)•改善的均一性:DAR1和DAR2≥85%;DAR4和DAR6≥65%•增强的疗效和安全性特征•与IgG1单抗兼容•与新型ADC(如双载荷ADC、双特异性ADC)和XDC(如AOC、APC)兼容•简单而稳健的偶联工艺•经验证的技术:7种ADC处于临床试验阶段,10个CMC项目,批量规模最高可达>2 kg。(2)巯基反应连接子技术。传统的链间半胱氨酸偶联使用马来酰亚胺连接子与抗体的巯基发生反应。然而,逆反应(逆Michael加成)可能导致载荷-连接子在循环中过早释放。为解决此问题,研发了X-LinC连接子以替代马来酰亚胺连接子,其显示出良好的血浆稳定性,并与WuXiDARx™完全兼容。制备均一DAR4 ADC的另一种方法是使用巯基重桥连接子。CysLink技术将稳定的巯基重桥连接子整合到该平台中。与传统连接子不同,CysLink版本生成的ADC具有更少的巯基错配和半抗体比例,并可与WuXiDARx™协同以提供额外的DAR选择(如DAR1)。 结论:WuXiDARx™、X-LinC和CysLink的组合提供了一个整合的解决方案,可利用临床验证最充分的偶联位点,从而帮助加速客户的ADC/XDC管线研发。
查看英文原文 English abstract
Background: Antibody drug conjugates (ADCs) and various types of bioconjugates (XDCs) have garnered increasing attention over the past decade. These novel payloads and payload combinations require advanced conjugation technologies to fully achieve their therapeutic potential. Conventionally, interchain cysteine coupling serves as the most clinically validated conjugation technologies. However, such methods have two major flaws: (1) heterogeneity from stochastic coupling (except for DAR8); and (2) instability during circulation due to maleimide retro-Michael addition. Solutions: To address these needs, WuXi XDC has built a platform through internal development and external collaboration. This platform includes two parts: (1) WuXiDARx™ conjugation technology WuXiDARx™ conjugates at interchain cystines which are the most clinical validated site, as 13 out of 18 commercial ADCs are developed through cysteine conjugation. This technology features: • Flexible DAR choices (WuXiDAR1 TM , WuXiDAR2 TM , WuXiDAR4 TM , WuXiDAR6 TM ) • Improved homogeneity: ≥ 85% for DAR1 and DAR2; or ≥ 65% for DAR4 and DAR6 • Enhanced efficacy and safety profiles • Compatibility with IgG1 mAb • Compatibility with novel ADCs (e.g., dual-payload ADCs, bispecific ADCs) and XDCs (e.g., AOCs, APCs) • Simple and robust conjugation process • Validated technology: 7 ADCs in clinical trials, 10 CMC projects, up to > 2 kg batch size (2) Thiol reactive connector technologies Conventional interchain cysteine conjugation uses maleimide connector to react with the thiol groups from the antibody. However, the reverse reaction (retro-Michael addition) may result in premature release of the payload-linkers in circulation. To solve this problem, X-LinC connector is developed to replace the maleimide connector, which has shown good plasma stability and is fully compatible with WuXiDARx TM . A different way to create homogeneous DAR4 ADCs is by using thiol-rebridging connectors. CysLink technology incorporates a stable thiol-rebridging connector into the platform. Unlike traditional connectors, the CysLink version produces ADCs with fewer thiol mismatches and half-antibody ratios, and it works with WuXiDARx TM to offer additional DAR options (e.g., DAR1). Conclusion: The combination of WuXiDARx TM , X-LinC, and CysLink offers an integrated solution to utilize the most clinically validated conjugation sites, which is helping accelerate ADCs/XDCs pipeline development from clients.
利益披露 Disclosure
Q. Fan, None.. H. Chen, None.. J. Huang, None.. L. Zhang, None.. Z. Wang, None.. D. Wei, None.. G. Wei, None.. Y. Zhao, None.. L. Wang, None.. C. Cheng, None.. M. Zhu, None.

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