Declerck Paul, Farouk Rezk Mourad
Laboratory for Therapeutic and Diagnostic Antibodies, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven - University of Leuven, Leuven, Belgium.
Biogen International GmbH, Zug, Switzerland.
Rheumatology (Oxford). 2017 Aug 1;56(suppl_4):iv4-iv13. doi: 10.1093/rheumatology/kex279.
Biosimilars are products that contain a similar version of the active substance of an already authorized original biologic medicinal product (reference medicinal product). Their development requires special consideration, as similarity to the reference agent needs to be established through a comprehensive comparability exercise. Given the complex nature of these agents, minor structural differences may emerge, but the process of biosimilarity determination is designed to ascertain that the nature and impact of these differences are not clinically significant. Determination of biosimilarity should follow quality-by-design principles, which provide a deep understanding of the product development process, guided by pre-defined objectives, process control and risk management. Compared with novel biologic development, biosimilar development places greater emphasis on establishing preclinical quality characteristics. Determination of comparability of quality characteristics includes assessment of physicochemical properties, biological activity, immunochemical properties, purity, impurity and quantity, with appropriate in vivo pharmacology studies being conducted thereafter. Head-to-head comparisons are then conducted to determine pharmacokinetic and pharmacodynamic characteristics, and efficacy, safety and tolerability in phase I and phase III clinical studies. Post-approval risk management requirements include implementation of pharmacovigilance systems and risk management through, for example, the conduct of pharmacoepidemiological studies. There are several biosimilars used in the field of rheumatology that are available in the European Union, or in development, that offer the potential to increase affordability/accessibility of biological treatment. The role of these agents in rheumatology will be determined by the confidence placed in them by rheumatologists. These prescribers should expect high-quality data evaluated by an extensive assessment process.
生物类似药是含有已获授权的原创生物药品(参比药品)活性物质类似版本的产品。其研发需要特殊考量,因为需要通过全面的可比性研究来确定与参比制剂的相似性。鉴于这些制剂的复杂性质,可能会出现微小的结构差异,但生物类似性的确定过程旨在确保这些差异的性质和影响在临床上不具有显著意义。生物类似性的确定应遵循设计质量原则,该原则在预定义目标、过程控制和风险管理的指导下,对产品研发过程有深入理解。与新型生物药研发相比,生物类似药研发更强调确立临床前质量特征。质量特征可比性的确定包括对物理化学性质、生物活性、免疫化学性质、纯度、杂质和含量的评估,随后进行适当的体内药理学研究。然后进行直接比较以确定药代动力学和药效学特征,以及在I期和III期临床研究中的疗效、安全性和耐受性。批准后的风险管理要求包括实施药物警戒系统以及通过开展例如药物流行病学研究进行风险管理。在欧盟有几种用于风湿病领域的生物类似药已上市或正在研发中,它们有可能提高生物治疗的可承受性/可及性。这些药物在风湿病学中的作用将由风湿病学家对它们的信心来决定。这些开处方者应期望通过广泛评估过程评估的高质量数据。