Assessment of Functional Characterization and Comparability of Biotherapeutics: a Review

The development of monoclonal antibody (mAb) biosimilars is a complex process. The key to their successful development and commercialization is an in-depth understanding of the key product attributes that impact safety and efficacy and the strategies to control them. Functional assessment of mAb is a crucial part of the comparability of biopharmaceutical drugs. The development of a relevant and robust functional assay requires an interdisciplinary approach and sufficient flexibility to balance regulatory concerns as well as dynamics and variability during the manufacturing process. Although many advanced tools are available to study and compare the potency and bioactivity of the protein, most of these techniques suffer from major shortcomings that limit their routine use. These include the complexity of the task, establishment of the relevance of the chosen method with the mechanism of action (MOA) of the biosimilar, cost and extended time of analysis, and often the ambiguity in interpretation of the resulting data. To overcome or to address these challenges, the use of multiple orthogonal state-of-the-art techniques is a necessary prerequisite.

Automated summary

The development of monoclonal antibody (mAb) biosimilars is a complex process that requires a deep understanding of key product attributes affecting safety and efficacy, as well as strategies to control them. Establishing a relevant and robust functional assay for mAb comparability demands an interdisciplinary approach and flexibility. However, current advanced tools often have major shortcomings limiting their routine use, highlighting the need for multiple orthogonal state-of-the-art techniques to address these challenges.