Kiesman William F, McPherson Andrew K, Diorazio Louis J, Van den Bergh Leo, Smith Peter D, Northall John M, Fettes Alec, Wang Tiejun, Mehlmann Martin, Raza Syed, Held Gary
Antisense Oligonucleotide Development and Manufacturing, Biogen, Inc., Cambridge, Massachusetts, USA.
Process Organic Chemistry, Ionis Pharmaceuticals, Inc., Carlsbad, California, USA.
Nucleic Acid Ther. 2021 Apr;31(2):93-113. doi: 10.1089/nat.2020.0909. Epub 2021 Feb 2.
The designation of starting materials (SMs) for pharmaceuticals has been a topic of great interest and debate since the first ICH quality guidance was published. The increase in the number and variety of commercialized oligonucleotides (antisense oligonucleotides-ASOs, small interfering RNAs-siRNAs, etc.) in recent years has reignited dialogue on this topic because of the unique complexity of the monomeric nucleotides and other contributory materials used to manufacture oligonucleotides. The SM working group in the European Pharma Oligonucleotide Consortium (EPOC) was formed to help establish simple, risk-based criteria to guide the justification of oligonucleotide SMs. This article provides a description of the common types of SMs, classes of SM impurities, and control strategies that will be helpful to maintain manufacturing consistency.
自首份国际人用药品注册技术协调会(ICH)质量指南发布以来,药品起始物料(SMs)的指定一直是备受关注和争议的话题。近年来,商业化寡核苷酸(反义寡核苷酸-ASOs、小干扰RNA-siRNAs等)的数量和种类不断增加,由于用于制造寡核苷酸的单体核苷酸和其他辅助材料具有独特的复杂性,这一话题的讨论再度升温。欧洲制药寡核苷酸联盟(EPOC)的起始物料工作组旨在帮助建立简单的、基于风险的标准,以指导寡核苷酸起始物料的合理性论证。本文介绍了常见的起始物料类型、起始物料杂质类别和控制策略,这些将有助于保持生产的一致性。