Biocon Biologics and Viatris get CHMP Nod for Abevmy
It is a Biosimilar to Avastin, Bevacizumab
Biocon Biologics, a subsidiary of Biocon announced that the European
Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending the marketing authoris ation of their biosimilar Bevacizumab, co-developed with Viatris, to be marketed as Abevmy (injection bevacizumab 100mg and 400mg).
Abevmy is a biosimilar to Roche’s
Avastin, prescribed for all indications including metastatic colorectal carcinoma, metastatic breast cancer, non-small-cell lung carcinoma, glioblastoma, ovarian, cervical and renal cancer as part of a specific regimen.
The decision of the European Commission (EC) is expected in May 2021, which, when approved, will grant marketing authorisation in the 27 European Union (EU) member countries and European Economic Area (EEA) member states of Norway, Iceland and Liechtenstein.
For the UK, the Medicines and Healthcare Products Regulatory Agency’s “reliance procedure” will be followed, and the UK marketing authorisation can be expected shortly after the EC decision.
Kiran Mazumdar-Shaw, Executive Chairperson, Biocon Biologics, said, “CHMP’s decision to recommend approval of our biosimilar Bevacizumab brings us a step closer to enable affordable access to this biologic therapy for cancer patients in the EU along with our partner Viatris. It is an outcome of our commitment to expand access for patients leveraging our science and global scale manufacturing for a range of biosimilars. Through Trastuzumab and Pegfilgrastim we are already making a
difference to the lives of cancer patients in several EU countries. We look forward to a final decision from the European Commission approving biosimilar Bevacizumab, which will add to our efforts in cancer care.”
Abevmy, Bevacizumab, is a recombinant “humanised” monoclonal antibody that selectively binds to human vascular endothelial growth factor (VEGF) and neutralises its biologic activity. Bevacizumab inhibits the formation of tumor vasculature, thereby inhibiting tumor growth.