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Current and future issues in the manufacturing and development of monoclonal antibodies

Journal

ADVANCED DRUG DELIVERY REVIEWS
Volume 58, Issue 5-6, Pages 707-722

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.addr.2006.05.002

Keywords

monoclonal antibodies; manufacturing; product testing; biological characterization; quality by design

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Despite a slow beginning, monoclonal antibodies have had many successes over the past decade. It is important that these successes continue, bringing more products for more indications to market. Although manufacturing is not the most common cause of product failure, product quality issues can delay antibody development. Manufacturing has depended on the triad of process validation, process control and product testing. Applying product knowledge proactively to manufacturing (quality by design) may allow greater flexibility and maintain or improve product quality. An integrated approach to biological characterization is an important aspect of product knowledge. Greater product knowledge also facilitates development in other disciplines. Independent of manufacturing strategy, there are a number of regulatory hurdles in initial and ongoing antibody development. These are described to help prevent unnecessary delays. Published by Elsevier B.V.

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