Bevacizumab biosimilar is under clinical development by Biocad and currently in Phase III for Non-Small Cell Lung Cancer. According to GlobalData, Phase III drugs for Non-Small Cell Lung Cancer have a 46% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Bevacizumab biosimilar’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Bevacizumab biosimilar overview
Bevacizumab biosimilar (Avegra) is a recombinant humanized monoclonal IgG1 antibody acts as an anti neoplastic agent. It is formulated as concentrate solution for intravenous route of administration. Bevacizumab is indicated for the treatment of cervical cancer, colorectal cancer, fallopian tube cancer, glioblastoma multiforme (gbm), kidney cancer (renal cell cancer), lung cancer, mammary ductal carcinoma, metastatic renal cell carcinoma, non-small cell lung cancer and peritoneal cancer
The drug candidate is under development for the treatment of non-small cell lung cancer, colorectal cancer and it was also under development for wet macular degeneration.
Biocad overview
JSC Biocad (Biocad) is a biotechnology company that conducts research and development services. The company develops, manufactures, and distributes generic pharmaceutical products. Its products portfolio comprise rituximab, bevacizumab, trastuzumab, prolgolimab, levilimab, netakimab and eculizumab. Biocad develops products in the form of suppositories, spray, and drops. The compay provides products under the brands Avegra, Herticad, Gerticad, Forteka, Extimia and Leucostim. It manufactures products in the therapeutic areas such as oncology, rare disease, autoimmune diseases, and infectious diseases. The company’s R&D centers are located in Lyubuchany, Neudorf and Frontovaya. It operates in Brazil, China, Russia, the UAE and Vietnam. Biocad is headquartered in Saint-Petersburg, Russia.
For a complete picture of Bevacizumab biosimilar’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
