Abstract
Biosimilar monoclonal antibodies directed against TNF-a for the treatment of IBD are being developed, yet the complexity of these molecules, together with factors related to their manufacture, have the potential to translate into clinically relevant differences in efficacy, safety and immunogenicity in biosimilar agents. It is important for the Canadian gastroenterology community to gain a full understanding of the important issues in the context of the development and entry into the marketplace of such biologic agents. © 2013 Pulsus Group Inc.
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CITATION STYLE
Devlin, S. M., Bressler, B., Bernstein, C. N., Fedorak, R. N., Bitton, A., Singh, H., & Feagan, B. G. (2013). Overview of subsequent entry biologics for the management of inflammatory bowel disease and Canadian Association of Gastroenterology position statement on subsequent entry biologics. Canadian Journal of Gastroenterology, 27(10), 567–571. https://doi.org/10.1155/2013/327120
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