生物分析
双特异性抗体
表征(材料科学)
药物开发
纳米技术
药代动力学
药品
计算生物学
药理学
化学
医学
生物
材料科学
抗体
单克隆抗体
免疫学
作者
Mark Ma,Kelly Colletti,Tong‐Yuan Yang,Sheldon S. Leung,Susan Pederson,Charles Hottenstein,Xiaohui Xu,Dominic Warrino,Eric Wakshull
出处
期刊:Bioanalysis
[Newlands Press Ltd]
日期:2019-03-01
卷期号:11 (5): 427-435
被引量:10
标识
DOI:10.4155/bio-2018-0146
摘要
Compared with conventional (monospecific) therapeutics, bispecific protein therapeutics present unique challenges for pharmacokinetic (PK) characterization – namely, the characterization of multiple functional domains as well as the consideration of biotransformation or interference by the formation of antitherapeutic antibodies against each functional domain. PK characterization is essential to the success of the overall drug development plan and for molecules with multiple binding domains; multiple bioanalytical methods may be needed to answer critical questions for each phase of drug development. The number of bispecific protein therapeutics entering drug development continues to increase, and therefore, a bioanalytical strategy for the PK characterization of bispecific molecules and study of their in vivo structure–function relationship is needed. This review presents case studies and a regulatory perspective.
科研通智能强力驱动
Strongly Powered by AbleSci AI