Remicade Simponi Legal Memorandum
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Remicade (Inflectra®), made by Regeneron Pharmaceuticals, is a biologic medicine, which is a form of biotechnology. It is used to treat arthritis, psoriasis, psoriatic arthritis, and juvenile idiopathic arthritis (JIA). The drug is composed of biologic agent, pegylated interferon alpha (PegAsn) and adalimumab (Humira®). The therapy works by activating
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The world’s first humanized anti-TNF antibody, Remicade Simponi is a 2018 approved medication, approved by FDA and EMA, for the treatment of rheumatoid arthritis, psoriasis, and ankylosing spondylitis. Its development and approval process was a significant milestone in the history of biopharmaceuticals. Remicade Simponi is made of purified proteins, which are modified from animal antibodies to ensure
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Remicade Simponi, which is a medicine created by Biogen, was launched in Europe and the US in 2012. It is one of the two types of humanized monoclonal antibodies, an immune checkpoint inhibitor designed to stop the immune system from attacking the body’s cells and tissues. Its first use in the US was for the treatment of psoriasis, and its marketed version was used for RA (osteoarthritis), a chronic inflammatory disease that affect
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Topic: Remicade Simponi Legal Memorandum Section: Evaluation of Alternatives Now I’d like to present a legal memorandum that evaluates Remicade Simponi: Section I: Legal Memorandum Overview Title of legal memorandum: Remicade Simponi Legal Memorandum Date: XXXX/XXXX/XXXX This legal memorandum evaluates Remicade Simponi (Infliximab) for the treatment of adult
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1. Remicade (Simponi) is an anti-tumor necrosis factor (TNF) medication. It was approved by the FDA in 2016, and as such, has significant market share. Remicade’s main competitors are Humira (AbbVie), Enbrel (EMD) and Erelzi (Novartis). However, these competitors are in the process of losing market share, and Remicade seems to be gaining share. 2. Historical background