Bio-Thera Reports the EMA’s Approval of Avzivi (Biosimilar, Avastin) for Treating Multiple Indications
Shots:
- The EMA has granted approval to the company’s Avzivi (bevacizumab), a biosimilar version of Avastin. Sandoz is responsible for marketing the drug across the EU
- The license and commercialization agreement b/w Bio-Thera and Sandoz was signed in Sep 2021, under which Bio-Thera had the development and manufacturing rights while Sandoz secured the commercialization rights worldwide
- Avzivi is a humanized mAb that works by inhibiting the binding of VEGF with its receptors to reduces neovascularization & induce blood vessels degradation, inhibiting tumor growth
Ref: Bio-Thera | Image: Bio-Thera| Press Release
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