Suppr超能文献

美国药学家协会全国生物技术会议短期课程:开发抗体药物偶联物的转化挑战:2012 年 5 月 24 日,加利福尼亚州圣地亚哥。

American Association of Pharmaceutical Scientists National Biotechnology Conference Short Course: Translational Challenges in Developing Antibody-Drug Conjugates: May 24, 2012, San Diego, CA.

机构信息

Novartis Pharmaceuticals, Clinical Pharmacology, Oncology Business Unit, Florham Park, NJ, USA.

出版信息

MAbs. 2013 Jan-Feb;5(1):5-12. doi: 10.4161/mabs.22909. Epub 2012 Dec 19.

Abstract

The American Association of Pharmaceutical Scientists (AAPS) National Biotechnology Conference Short Course "Translational Challenges in Developing Antibody-Drug Conjugates (ADCs)," held May 24, 2012 in San Diego, CA, was organized by members of the Pharmacokinetics, Pharmacodynamics and Drug Metabolism section of AAPS. Representatives from the pharmaceutical industry, regulatory authorities, and academia in the US and Europe attended this short course to discuss the translational challenges in ADC development and the importance of characterizing these molecules early in development to achieve therapeutic utility in patients. Other areas of discussion included selection of target antigens; characterization of absorption, distribution, metabolism, and excretion; assay development and hot topics like regulatory perspectives and the role of pharmacometrics in ADC development. MUC16-targeted ADCs were discussed to illustrate challenges in preclinical development; experiences with trastuzumab emtansine (T-DM1; Genentech) and the recently approved brentuximab vedotin (Adcetris; Seattle Genetics) were presented in depth to demonstrate considerations in clinical development. The views expressed in this report are those of the participants and do not necessarily represent those of their affiliations.

摘要

美国制药科学家协会(AAPS)国家生物技术会议短期课程“开发抗体药物偶联物(ADC)的转化挑战”于 2012 年 5 月 24 日在加利福尼亚州圣地亚哥举行,由 AAPS 药代动力学、药效学和药物代谢分会的成员组织。来自美国和欧洲的制药行业、监管机构和学术界的代表参加了这个短期课程,讨论 ADC 开发中的转化挑战,以及在开发早期对这些分子进行特征描述的重要性,以实现对患者的治疗效果。其他讨论领域包括靶抗原的选择;吸收、分布、代谢和排泄的特征;检测方法的开发,以及监管观点和药物代谢动力学在 ADC 开发中的作用等热门话题。讨论了 MUC16 靶向 ADC 以说明临床前开发中的挑战;深入介绍了曲妥珠单抗美坦新(T-DM1;基因泰克)和最近批准的 Brentuximab vedotin(Adcetris;西雅图遗传学)的经验,以展示临床开发中的考虑因素。本报告中表达的观点是与会者的观点,不一定代表他们所在机构的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b55/3564886/256c17ceb27c/mabs-5-5-g1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验