Biosimilar monoclonal antibodies approved for use in the EU

Journal Title: Generics and Biosimilars Initiative Journal - Year 2014, Vol 3, Issue 1

Abstract

Two biosimilar TNF-alfa monoclonal antibody (mAb) products were approved for clinical use in the European Union on 10 September 2013, following a positive opinion by the Committee for Medicinal Products for Human Use (CHMP) in July 2013. The products, with trade names Remsima and Inflectra (INNs infliximab) contain an identical mAb. This approval shows the feasibility of using the biosimilar pathway for mAbs and paves the way for further biosimilar mAb products.

Authors and Affiliations

Meenu Wadhwa, Robin Thorpe

Keywords

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  • EP ID EP354141
  • DOI 10.5639/gabij.2014.0301.004
  • Views 169
  • Downloads 0

How To Cite

Meenu Wadhwa, Robin Thorpe (2014). Biosimilar monoclonal antibodies approved for use in the EU. Generics and Biosimilars Initiative Journal, 3(1), 9-10. https://www.europub.co.uk/articles/-A-354141