| Literature DB >> 25821140 |
Alexander Jarasch1, Hans Koll1, Joerg T Regula1, Martin Bader1, Apollon Papadimitriou1, Hubert Kettenberger2.
Abstract
Therapeutic antibodies and antibody derivatives comprise the majority of today's biotherapeutics. Routine methods to generate novel antibodies, such as immunization and phage-display, often give rise to several candidates with desired functional properties. On the contrary, resource-intense steps such as the development of a cell line, a manufacturing process, or a formulation, are typically carried out for only one candidate. Therefore, "developability," that is, the likelihood for the successful development of a lead candidate into a stable, manufacturable, safe, and efficacious drug, may be used as an additional selection criterion. Employing a set of small-scale, fast, and predictive tests addressing biochemical and biophysical features, as well as in vivo fate can help to identify a clinical candidate molecule with promising properties at an early stage of drug development. This article gives an overview of existing methods for developability testing and shows how these assays can be interlaced in the lead selection process.Keywords: analytical biochemistry; bioinformatics; biotechnology; deamidation; degradation products; immune response; in silico modeling; monoclonal antibody; oxidation; pharmacokinetics
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Year: 2015 PMID: 25821140 DOI: 10.1002/jps.24430
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534