Netherlands-based biopharmaceutical company Synthon announced on 18 July 2012 that it has entered into a global licensing agreement with Amgen and Watson Pharmaceuticals for the clinical development and testing of biosimilar trastuzumab as an alternative to Roche’s blockbuster anticancer agent Herceptin. The deal follows the results of a phase I trial reported on 22 March 2012 showing bioequivalence between Synthon’s trastuzumab and Herceptin [1].
Deal struck over development of Herceptin biosimilar
Biosimilars/News
|
Posted 03/08/2012
0
Post your comment
The deal enables Watson Pharmaceuticals to oversee all phase III clinical testing in breast cancer patients as well as the global manufacturing and commercialisation. Synthon will provide transitional support in return for an undisclosed initial payment, and potentially gains a milestone fee and a portion of net sales.
Meanwhile, Synthon will continue to develop independently a HER2-targeted antibody-drug conjugate candidate using proprietary technology.
Trastuzumab and Synthon’s biosimilar are humanised monoclonal antibodies that target the HER2 receptor, which was originally found to be over expressed on breast cancer cells. Trastuzumab is currently used to treat both breast cancer and gastric cancer.
The patents on Herceptin are set to expire in Europe in July 2014 and in the US in June 2019 [2]. Generics giants Hospira and Stada are also reportedly working on their own biosimilar versions of trastuzumab, so it looks like there will be no shortage of competition once the patents on Herceptin expire.
Related articles
Hospira looks to biosimilars and increased use of generics for growth
The market for global and European biosimilars
References
1. GaBI Online - Generics and Biosimilars Initiative. Also noted on biosimilars: 30 March 2012: Bioequivalence of biosimilar trastuzumab to Herceptin proven in phase I trial [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2012 Aug 3]. Available from: www.gabionline.net/Biosimilars/General/Also-noted-on-biosimilars-30-March-2012
2. GaBI Online - Generics and Biosimilars Initiative. US$54 billion worth of biosimilar patents expiring before 2020 [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2012 Aug 3]. Available from: www.gabionline.net/Biosimilars/Research/US-54-billion-worth-of-biosimilar-patents-expiring-before-2020
Source: Amgen, Synthon
Research
Reaching ESG goals in pharmaceutical development
What is the future for the US biosimilar interchangeability designation
General
Samsung Bioepis wins Pyzchiva case; Regeneron patent rulings threaten foreign biosimilars
Chinese biosimilars go global: growth, partnerships, and challenges
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Related content
EMA recommends approval for insulin glargine biosimilar Ondibta and denosumab biosimilar Osqay
FDA approves denosumab biosimilars Osvyrti and Jubereq, Boncresa and Oziltus
FDA approves aflibercept biosimilar Eydenzelt and label expansion for adalimumab biosimilar Yuflyma
ANVISA approves biosimilars for denosumab, trastuzumab, and aflibercept
EMA recommends approval for insulin glargine biosimilar Ondibta and denosumab biosimilar Osqay
Biosimilars/News Posted 16/01/2026
FDA approves denosumab biosimilars Osvyrti and Jubereq, Boncresa and Oziltus
Biosimilars/News Posted 07/01/2026
FDA approves aflibercept biosimilar Eydenzelt and label expansion for adalimumab biosimilar Yuflyma
Biosimilars/News Posted 05/12/2025
ANVISA approves biosimilars for denosumab, trastuzumab, and aflibercept
Biosimilars/News Posted 05/12/2025
The best selling biotechnology drugs of 2008: the next biosimilars targets
Post your comment