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Article source: Medical Rubik's Cube Info
On December 1, Toyo Pharmaceuticals announced that its self-developed bevacizumab injection TAB008 (trade name: Puxintin, intended to be used in English Pusintin) was approved by the National Medical Products Administration (NMPA) for the treatment of advanced, Metastatic or recurrent non-squamous non-small cell lung cancer and metastatic colorectal cancer
Bevacizumab is an anti-vascular endothelial cell growth factor monoclonal antibody (anti-VEGF mAb) that can specifically bind to VEGF and block the binding of VEGF to its receptors, thereby reducing angiogenesis and inducing existing blood vessels Degenerate, inhibit tumor growth
Avastin was approved by the FDA for the first time in February 2004, and then successively listed in the European Union, Japan, China and other countries
As a broad-spectrum anti-tumor drug, bevacizumab has become a standard program recommended by the global guidelines for the treatment of a variety of malignant tumors.
At present, in addition to the original research, seven biosimilars of bevacizumab have been approved for marketing in China, namely Qilu Pharmaceutical, Cinda Bio, Hengrui Pharmaceutical, Boan Bio, Biotech, Betta Bio and Toyo Pharmaceutical industry
Note: The original text has been deleted