作者
Parag Goyal,Bhavesh Vats,Malini Subbarao,Chethan Gejjalagere Honnappa,Pradeep Kabadi,Sheija Rohil,Arnab Bera,Gaurav R Mehta,Harish V. Pai,Laxmi Adhikari,Ranitendranath Tagore,Shulagna Sharma,Roopa Venkatachala,Pradip Nair,Shankara Annegowda,Abhilashi Sahu,Shruti Trivedi,Namrata Shastri,Yatika Gokhale,Roshni Thomas,Anushikha Thakur,Melepurath Deepa,Umamaheshwara Rao K,Ramakrishnan Melarkode,Rajesh Ullanat
摘要
Bevacizumab (BEV) is a recombinant humanized monoclonal immunoglobulin G1 antibody that binds to vascular endothelial growth factor (VEGF)-A and acts as an antiangiogenic agent. It is approved for treatment of many cancer indications, including metastatic colorectal cancer and nonsquamous non-small cell lung cancer.The analytical similarity of the BEV biosimilar MYL-1402O to reference BEV sourced from the European Union and United States was assessed using physicochemical and functional tests to support the clinical development of MYL-1402O. Assessment of physicochemical and analytical similarity showed that MYL-1402O has the same amino acid sequence and similar posttranslational modification profile as the reference BEV products.The functional and biologic activity of MYL-1402O assessed using inhibition of VEGF-induced cell proliferation in human umbilical vein endothelial cells, inhibition of VEGF-induced VEGF receptor 2 phosphorylation, and fragment antigen and fragment crystallizable receptor binding, was comparable to reference BEV products.The totality of the data assessment confirms the high degree of similarity of MYL-1402O to reference BEV with respect to physicochemical and in vitro functional properties. The product quality data presented here, along with data from phase 1 clinical studies, demonstrate the similarity of MYL-1402O to reference BEV products, supporting further clinical development of this BEV biosimilar.