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Challenges in developing bioanalytical assays for characterization of antibody-drug conjugates.

机译:开发用于表征抗体-药物偶联物的生物分析测定法面临的挑战。

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摘要

With more than 34 targets being investigated and nearly 20 clinical trials at various phases of development, antibody-drug conjugates (ADCs) hold a lot of promise for improving oncological malignancy therapy. This therapeutic strategy designed to specifically or preferentially deliver a cytotoxic agent to tumor cells through conjugation to a monoclonal antibody is not new. Although this approach is relatively simple conceptually, the history of ADCs clearly attests to the high degree of complexity in their development. Each component of an ADC is important to achieve efficacy with minimal toxicity, and the ability to monitor this multicomponent therapeutic entity is deemed to be critical for their successful optimization. In this article we review the different bioanalytical strategies that have been implemented to characterize various ADCs and discuss the challenges and issues associated with these approaches.
机译:抗体药物偶联物(ADC)的研发目标涉及34个以上的靶标,并且在不同的开发阶段进行了近20项临床试验,因此有望改善肿瘤的恶性肿瘤治疗。通过与单克隆抗体结合而专门或优先向肿瘤细胞递送细胞毒剂的这种治疗策略并不是什么新鲜事。尽管此方法在概念上相对简单,但ADC的历史清楚地证明了其开发的高度复杂性。 ADC的每个成分对于以最小的毒性实现功效都很重要,并且监视这种多成分治疗实体的能力被视为对其成功进行优化至关重要。在本文中,我们回顾了已实现的表征各种ADC的不同生物分析策略,并讨论了与这些方法相关的挑战和问题。

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