| Literature DB >> 26395532 |
Shomron Ben-Horin1, Graham A Heap2,3, Tariq Ahmad2,4, HoUng Kim5, TaekSang Kwon5, Yehuda Chowers6.
Abstract
Biopharmaceuticals or 'biologics' have revolutionized the treatment of many diseases. However, some patients generate an immune response to such drugs, potentially limiting clinical efficacy and safety. Infliximab (Remicade(®)) is a monoclonal antibody used to treat several immune-mediated inflammatory disorders. A biosimilar of infliximab, CT-P13 (Remsima(®), Inflectra(®)), has recently been approved in Europe for all indications in which infliximab is approved. Approval of CT-P13 was based in part on extrapolation of clinical trial data from two indications (rheumatoid arthritis and ankylosing spondylitis) to all other indications, including inflammatory bowel disease. This review discusses the validity of extrapolating immunogenicity data across indications - a process adopted by the EMA as part of their biosimilar approval process - with a focus on CT-P13.Entities:
Keywords: CT-P13; biologics; biosimilars; extrapolation; immunogenicity; inflammatory bowel disease; infliximab
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Year: 2015 PMID: 26395532 DOI: 10.1586/17474124.2015.1091307
Source DB: PubMed Journal: Expert Rev Gastroenterol Hepatol ISSN: 1747-4124 Impact factor: 3.869