US biotechnology company Biogen Idec (Biogen) and Korean electronics giant Samsung announced on 17 December 2013 that Biogen has exercised its right to enter into an agreement to commercialize anti-tumour necrosis factor (TNF) biosimilar product candidates in Europe.
Biogen and Samsung make deal for marketing anti-TNF biosimilars
Biosimilars/News
|
Posted 17/01/2014
0
Post your comment
Biogen will manufacture and market in Europe a number of anti-TNF biosimilars for inflammatory diseases such as rheumatoid arthritis and Crohn’s disease. The agreement is part of the joint venture (called Samsung Bioepis) Biogen made back in December 2011 with Samsung’s specialized biologicals unit, Samsung Biologics [1].
Mr Tony Kingsley, Biogen’s Executive Vice President of Global Commercial Operations viewed the deal as ‘a unique opportunity for us to leverage our experience in developing and manufacturing high-quality biologic[al]s in therapeutic areas where we are deeply focused’. While Mr Christopher Hansung Ko, CEO of Samsung Bioepis, believes that ‘this agreement will further serve as a solid foundation for Samsung Bioepis to develop into a worldwide biosimilar leader’.
Samsung plans to launch biosimilars by 2015 at half the price that patients in the US and Europe currently pay and is expecting to achieve annual revenues from biologicals of US$1.8 trillion by 2020 [2].
Related article
Samsung to launch biosimilars by 2015 at half the current prices
References
1. GaBI Online - Generics and Biosimilars Initiative. Samsung makes biosimilars deal with Biogen Idec [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2014 Jan 17]. Available from: www.gabionline.net/Biosimilars/News/Samsung-makes-biosimilars-deal-with-Biogen-Idec
2. GaBI Online - Generics and Biosimilars Initiative. Samsung halts biosimilar rituximab development [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2014 Jan 17]. Available from: www.gabionline.net/Biosimilars/News/Samsung-halts-biosimilar-rituximab-development
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 © 2014 Pro Pharma Communications International. All Rights Reserved.
Source: Biogen Idec, Samsung Bioepis
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