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Biosimilar Therapeutic Monoclonal Antibodies: Gaps in Science Limit Development of an Industry Standard for Their Regulatory Approval, Part 1

机译:生物仿制药单克隆抗体:科学上的空白限制了其监管批准的行业标准的制定,第1部分

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摘要

Biosimilars are biologically derived pharmaceuticals intended to have clinical similarity to a legally marketed innovator product when that product's patent or market exclusivity has expired. By contrast with generic small-molecule drugs, clinical performance of a biologic pharmaceutical is a function of its structural complexity and higher-order structure (HOS). Biomanufacturing controls of such complex products cannot fully ensure chemical similarity between an innovator product and putative biosimilar because minor differences in chemical modifications and HOS can significantly alter a product's safety and efficacy.
机译:生物仿制药是生物衍生的药品,旨在在该产品的专利或市场专有权到期后与合法销售的创新产品具有临床相似性。与普通的小分子药物相比,生物药物的临床性能是其结构复杂性和高阶结构(HOS)的函数。此类复杂产品的生物制造控制无法完全确保创新产品与推定的生物仿制药之间的化学相似性,因为化学修饰和HOS的微小差异会大大改变产品的安全性和有效性。

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