| Literature DB >> 31900688 |
Herman Gill1, Richard Seipert2, Vincent M Carroll3, Alexandra Gouasmat3, Jian Yin2, Annie Ogasawara4, Isabella de Jong2, Minh Michael Phan4, Xiangdan Wang4, Jihong Yang4, Ohad Ilovich3, Jan Marik4, Simon-Peter Williams4.
Abstract
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 89Zr-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.Entities:
Keywords: Immuno-PET; Positron Emission Tomography; cancer immunotherapy; chemistry; clinical trial; manufacturing, and controls
Year: 2020 PMID: 31900688 DOI: 10.1208/s12248-019-0392-0
Source DB: PubMed Journal: AAPS J ISSN: 1550-7416 Impact factor: 4.009