South Korean electronics giant Samsung and biotechnology company Biogen Idec’s joint venture Samsung Bioepis announced on 20 November 2017 that it had received European Commission (EC) approval for its biosimilar trastuzumab product Ontruzant (SB3).
EC approval for trastuzumab biosimilar Ontruzant
Biosimilars/News
|
Posted 01/12/2017
0
Post your comment

Trastuzumab is a monoclonal antibody that interferes with the human epidermal growth factor receptor 2 (HER2)/neu receptor. In some cancers, notably certain types of breast cancer, HER2 is overexpressed, and causes cancer cells to reproduce uncontrollably. Trastuzumab is therefore used to treat certain breast cancers.
The approval by the EC follows the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) positive recommendation on 15 September 2017 [1].
Ontruzant is the first trastuzumab biosimilar to be approved in Europe. It has been approved for the treatment of early breast cancer, metastatic breast cancer and metastatic gastric cancer
The approval marks the fourth biosimilar approved in Europe for Samsung Bioepis. The company has also received approval for Benepali (etanercept), Flixabi (infliximab) and Imraldi (adalimumab) [2].
Ontruzant will be commercialized in the EU by Merck Sharp and Dohme (MSD), which is known as Merck in the US and Canada.
Related article
Biosimilars of trastuzumab
References
1. GaBI Online - Generics and Biosimilars Initiative. Adalimumab and trastuzumab biosimilars approved in South Korea [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Dec 1]. Available from: www.gabionline.net/Biosimilars/News/Adalimumab-and-trastuzumab-biosimilars-approved-in-South-Korea
2. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in Europe [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2017 Dec 1]. 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: Samsung Bioepis
Research
Positive safety and efficacy primary endpoint results for AVT05 (golimumab proposed biosimilar)
General
Biologicals and biosimilars available for IBD in Canada
Biosimilar medicines on the Pharmaceutical Benefits Scheme in Australia
EC approves eight biosimilars, eight more await final authorization

Biosimilars/News Posted 18/02/2025
EMA recommends approval for tocilizumab biosimilar Avtozma and filgrastim biosimilar Zefylti

Biosimilars/News Posted 28/01/2025
The best selling biotechnology drugs of 2008: the next biosimilars targets

Post your comment