Genentech Research and Early Development, South San Francisco, California, USA.
Genentech Pharmaceutical Technical Development, South San Francisco, California, USA.
AAPS J. 2020 Jan 3;22(2):22. doi: 10.1208/s12248-019-0392-0.
Immuno-PET is a molecular imaging technique utilizing positron emission tomography (PET) to measure the biodistribution of an antibody species labeled with a radioactive isotope. When applied as a clinical imaging technique, an immuno-PET imaging agent must be manufactured with quality standards appropriate for regulatory approval. This paper describes methods relevant to the chemistry, manufacturing, and controls component of an immuno-PET regulatory filing, such as an investigational new drug application. Namely, the production, quality control, and characterization of the immuno-PET clinical imaging agent, ZED8, an Zr-labeled CD8-specific monovalent antibody as well as its desferrioxamine-conjugated precursor, CED8, is described and evaluated. PET imaging data in a human CD8-expressing tumor murine model is presented as a proof of concept that the imaging agent exhibits target specificity and comparable biodistribution across a range of desferrioxamine conjugate loads.
免疫 PET 是一种利用正电子发射断层扫描(PET)测量放射性同位素标记的抗体种类的生物分布的分子成像技术。当作为临床成像技术应用时,免疫 PET 成像剂必须按照适合监管批准的质量标准制造。本文描述了与免疫 PET 监管申报(如研究性新药申请)的化学、制造和控制部分相关的方法。具体而言,描述和评估了免疫 PET 临床成像剂 ZED8 的生产、质量控制和特性,ZED8 是一种 Zr 标记的 CD8 特异性单价抗体及其去铁胺缀合物前体 CED8。在人 CD8 表达肿瘤鼠模型中呈现 PET 成像数据,作为该成像剂表现出靶向特异性和在一系列去铁胺缀合物负载下可比生物分布的概念验证。