Biosimilars Therapeutics Pipeline Analysis 2018, Clinical Trials & Results, Patents, Designations, Collaborations, and Other Developments

CITY, Country, 2019-Jul-16 — /EPR Network/ —

Biosimilar are biological products that show similar biological action as the U.S. Food and Drug Administration (USFDA) approved biologics. According to the U.S. Federal Code of Regulation, the biologic is a virus, toxin, antitoxin, or therapeutic serum valid for the treatment of a disease.

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Biosimilars become a potential cost-saving alternative and provide the similar effects as biologics, thus, are being prescribed with confidence. M923 of Momenta Pharmaceuticals Inc. is a proposed adalimumab biosimilar for the treatment of plaque psoriasis. Biocon Ltd. is also developing a wide portfolio of monoclonal antibody biosimilars for the treatment of cancer, diabetes, and rheumatoid arthritis.

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Novartis AG is developing GP2018 for the treatment of autoimmune diseases, such as rheumatoid arthritis and psoriasis. Samsung Bioepis Co. Ltd. has a robust biosimilar pipeline and is developing two major biosimilars, which are currently in the Phase III stage of development, including SB8 (bevacizumab biosimilar) for the treatment of non-small lung cancer, and SB11 (ranibizumab biosimilar) for the treatment of age-related macular degeneration. Some other companies having the pipeline of biosimilars include Biogen Inc., and Celltrion Inc. among others.

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  • The report provides a comprehensive understanding of the pipeline activities covering all drug candidates under various stages of development, with the detailed analysis of pipeline and clinical trials.
  • Pipeline analysis of drugs by phases includes product description and development activities including information about clinical results, designations, collaborations, licensing, grants, technology, and others.

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