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使用位点特异性化学偶联法合成抗体药物偶联物的良好生产规范策略:第一代AJICAP

Good Manufacturing Practice Strategy for Antibody-Drug Conjugate Synthesis Using Site-Specific Chemical Conjugation: First-Generation AJICAP.

作者信息

Matsuda Yutaka, Clancy Colin, Tawfiq Zhala, Robles Veronica, Mendelsohn Brian A

机构信息

Ajinomoto Bio-Pharma Services, 11040 Roselle Street, San Diego, California 92121, United States.

出版信息

ACS Omega. 2019 Nov 26;4(24):20564-20570. doi: 10.1021/acsomega.9b02419. eCollection 2019 Dec 10.

Abstract

The development of antibody-drug conjugates (ADCs) is in great demand in the oncology field. With the goal of maximizing the therapeutic index, the conjugation technology to produce ADCs has been shifted to a site-specific manner; however, it is still challenging to establish robust and scalable synthetic processes. We have developed a chemical conjugation platform termed AJICAP for site-specific ADC synthesis using IgG Fc-affinity peptides. Here, we report the preparation of site-specific ADCs based on first-generation AJICAP technology for use in good laboratory practice studies. Analysis of the final ADC product was conducted using validated systems and good manufacturing practice. This work may not only prompt further biological studies of AJICAP-ADC but also establish a strategy to provide well-documented manufacturing data to enable new drug application filings (e.g., investigational new drug applications) for site-specific ADCs.

摘要

抗体药物偶联物(ADC)的研发在肿瘤学领域有着巨大需求。为了实现治疗指数最大化,用于生产ADC的偶联技术已转向位点特异性方式;然而,建立稳健且可扩展的合成工艺仍具有挑战性。我们开发了一种名为AJICAP的化学偶联平台,用于使用IgG Fc亲和肽进行位点特异性ADC合成。在此,我们报告基于第一代AJICAP技术制备的位点特异性ADC,用于良好实验室规范研究。使用经过验证的系统和良好生产规范对最终的ADC产品进行了分析。这项工作不仅可能促使对AJICAP-ADC进行进一步的生物学研究,还可能建立一种策略,提供详细记录的生产数据,以便为位点特异性ADC进行新药申请备案(例如,研究性新药申请)。

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