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ECCO position statement: The use of biosimilar medicines in the treatment of inflammatory bowel disease (IBD)

机译:ECCO立场声明:使用生物仿制药治疗炎症性肠病(IBD)

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摘要

Biologics have become key agents for the management of Crohn's disease and ulcerative colitis. Biosimilars are biological medicines similar to previously authorized biologics and are already available in some countries. This ECCO Position Statement defines the collective view of European specialist in inflammatory bowel disease (IBD) concerning biosimilars. Biosimilars are not comparable to generic small molecules, since both efficacy and toxicity are difficult to predict due to subtle molecular changes that can have profound effects on clinical efficacy and immunogenicity. Direct evidence of safety and benefit from clinical trials in IBD, post-marketing pharmacoviligance, and unequivocal identification of the product as a biosimilar should be requirements before approval. Switching from an established biologic to a biosimilar to save costs is likely to be as inappropriate and inefecctive as switching between current biologics that act on the same target, except when there is loss of response.
机译:生物制剂已成为克罗恩氏病和溃疡性结肠炎治疗的关键药物。生物仿制药是与先前授权的生物仿制药相似的生物药品,并且在某些国家已经可用。该ECCO立场声明定义了欧洲炎症性肠病(IBD)专家有关生物仿制药的集体观点。生物仿制药无法与通用小分子药物相比,因为由于细微的分子变化难以预测疗效和毒性,而这些细微变化会对临床疗效和免疫原性产生深远影响。在批准之前,应要求提供直接安全性证据并能从IBD中的临床试验,上市后的药敏性以及将产品明确标识为生物仿制药中受益。从既有的生物制剂转换为生物仿制药以节省成本,就像在当前作用于同一靶标的生物制剂之间进行转换一样,除非失去反应,否则这种做法是不适当的且无效率的。

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