On 13 July 2017, three rituximab biosimilars, Blizima, Rituzena (previously Tuxella) and Ritemvia, received European Commission (EC) approval.
EC approval for three rituximab biosimilars
Biosimilars/News
|
Posted 08/09/2017
0
Post your comment
Rituximab is a chimeric monoclonal antibody against the protein CD20, which is primarily found on the surface of immune system B cells. Rituximab destroys B cells and is therefore used to treat diseases that are characterized by excessive number of B cells, overactive B cells or dysfunctional B cells. This includes many lymphomas, leukaemias, transplant rejection, and autoimmune disorders.
The approval by the EC follows the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) positive recommendation on 19 May 2017 [1].
All three rituximab biosimilars are produced by South Korean biotechnology company Celltrion. The company also has an infliximab biosimilar approved in Europe, as well as another rituximab biosimilar. Remsima (infliximab) was approved in September 2013 and Truxima (rituximab) was approved in February 2017 [2].
The four-name strategy for rituximab is believed to be a tactic to generate greater total market share for its biosimilar and allow Celltrion to hand out distribution rights to several different companies. The company has already used a similar strategy for its infliximab biosimilar, which has two names – Inflectra and Remsima – with Hospira (now Pfizer) using Inflectra and Celltrion Remsima.
Related article
Biosimilars of rituximab
References
1. GaBI Online - Generics and Biosimilars Initiative. EMA approval for insulin and rituximab biosimilars [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Sep 8]. Available from: www.gabionline.net/Biosimilars/News/EMA-approval-for-insulin-and-rituximab-biosimilars
2. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in Europe [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Sep 8]. Available from: www.gabionline.net/Biosimilars/General/Biosimilars-approved-in-Europe
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2017 Pro Pharma Communications International. All Rights Reserved.
Source: EMA
Research
HHS push to ‘genericize’ biosimilars sparks backlash
Biosimilar interchangeability: a necessary fix, but not a silver bullet
General
Medicines for Europe calls for Biotech Act reforms to address ‘biosimilar void’
SBR issues position statement on safe originator biological/biosimilar interchangeability
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Related content
Canada approves multiple denosumab and ustekinumab biosimilars as global competition grows
FDA approves Zimrixby (rituximab) and Garzulys (insulin aspart) biosimilars
EMA recommends approval for biosimilar pegfilgrastim Cavoley
FDA approves first interchangeable ranibizumab biosimilar Ranluspec
Canada approves multiple denosumab and ustekinumab biosimilars as global competition grows
Biosimilars/News Posted 15/09/2026
FDA approves Zimrixby (rituximab) and Garzulys (insulin aspart) biosimilars
Biosimilars/News Posted 02/09/2026
FDA approves first interchangeable ranibizumab biosimilar Ranluspec
Biosimilars/News Posted 04/08/2026
The best selling biotechnology drugs of 2008: the next biosimilars targets
Post your comment