Samsung Bioepis and AffaMed to start trastuzumab trial in China

Biosimilars/News | Posted 17/01/2020 post-comment0 Post your comment

China’s National Medical Products Administration (NMPA), formerly the China Food and Drug Administration (CFDA) has granted approval for partners Samsung Bioepis and AffaMed Therapeutics (AffaMed) to start a phase III trial for their trastuzumab product, SB3.

Breast cancer V15J22

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 and gastric cancers, HER2 is overexpressed, and causes cancer cells to reproduce uncontrollably. Trastuzumab is therefore used to treat certain breast and gastric cancers.

SB3 has already been approved as Samfenet in Korea in November 2017 [1] and as Ontruzant in Europe and the US in November 2017 and January 2019, respectively [2, 3].

The clinical trial will be the first that Samsung Bioepis has carried out in China. It is planned to enrol 208 breast cancer patients and is expected to start in the first quarter of 2020. The aim of the trial is to demonstrate that SB3 is not different from the reference drug, Herceptin (trastuzumab), in terms of safety and efficacy.

The trial will be conducted in collaboration with AffaMed, a biopharmaceutical company focused on identifying and licensing late-stage candidates for commercialization. AffaMed was founded and funded by C-Bridge Capital. Samsung Bioepis signed a licensing agreement with China-based C-Bridge Capital in February 2019 to develop and commercialize next-generation copy biologicals in China [4].

Related article
Bio-Thera gains Chinese approval for adalimumab copy biological and starts ustekinumab trial

References
1. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in South Korea [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2020 Jan17]. Available from: www.gabionline.net/Biosimilars/General/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 2020 Jan17]. Available from: www.gabionline.net/Biosimilars/General/Biosimilars-approved-in-South-Korea
3. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in the US [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2020 Jan17]. Available from: www.gabionline.net/Biosimilars/General/Biosimilars-approved-in-the-US
4. GaBI Online - Generics and Biosimilars Initiative. Samsung Bioepis makes deals for copy biologicals in China [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2020 Jan17]. Available from: www.gabionline.net/Pharma-News/Samsung-Bioepis-makes-deals-for-copy-biologicals-in-China

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 © 2020 Pro Pharma Communications International. All Rights Reserved.

Source: Korea Biomedical Review, Pulse

comment icon Comments (0)
Post your comment
Related content
Canada approves pegfilgrastim biosimilar Armlupeg
Pegfilgrastim DrugBank V18K30
Biosimilars/News Posted 20/11/2024
FDA approves fifth ustekinumab biosimilar Imuldosa
11453696_l
Biosimilars/News Posted 13/11/2024
Most viewed articles
About GaBI
Home/About GaBI Posted 06/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
Home/Guidelines Posted 08/10/2010