从抗体-药物偶联物的临床发展中吸取教训

Q1 Pharmacology, Toxicology and Pharmaceutics
Robert Lyon
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引用次数: 40

摘要

抗体-药物偶联物(ADC)领域的临床研究进入者数量显著增加。这些药物中的许多采用了在过去十年中发展起来的较新的偶联技术,这些技术赋予了用它们制备的adc各种属性,包括稳定性、效力和均匀性。在许多情况下,这些新的adc在活性和毒理学的临床前模型中明显优于早期的技术,但这些改进转化为临床的程度才刚刚开始被看到。目前,这些技术中的许多都是通过在相似的患者群体中针对相同的抗原进行正面竞争,从而可以直接比较它们的临床性能。随着这些经验的教训反馈到发现研究中,未来的ADC设计迭代有望将改进的治疗方法带入临床。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drawing lessons from the clinical development of antibody-drug conjugates

The antibody-drug conjugate (ADC) field has seen a remarkable expansion in the number of entrants in clinical studies. Many of these agents employ newer conjugation technologies that have been developed over the last decade that confer various attributes to the ADCs prepared with them, including stability, potency, and homogeneity. In many cases, these new ADCs appear demonstrably superior to earlier technologies in preclinical models of activity and toxicology, but the degree to which these improvements will translate to the clinic is only starting to be seen. Many of these technologies are now competing head-to-head by targeting the same antigen in similar patient populations, allowing for a direct comparison of their clinical performance properties. As lessons from these experiences feed back into discovery research, future iterations of ADC design may be expected to bring improved therapeutics into the clinic.

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来源期刊
Drug Discovery Today: Technologies
Drug Discovery Today: Technologies Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
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期刊介绍: Discovery Today: Technologies compares different technological tools and techniques used from the discovery of new drug targets through to the launch of new medicines.
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