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2020 年生物分析近期问题白皮书:混合测定法的生物变异度、声质谱、高分辨质谱、数据完整性、内源性化合物、微采样和微生物组(-关于行业/监管机构对 LCMS 生物疗法的生物变异度的共识建议、混合测定法中的高级应用、质谱法规挑战、小分子、肽和寡核苷酸的创新)。

2020 White Paper on Recent Issues in Bioanalysis: BMV of Hybrid Assays, Acoustic MS, HRMS, Data Integrity, Endogenous Compounds, Microsampling and Microbiome ( - Recommendations on Industry/Regulators Consensus on BMV of Biotherapeutics by LCMS, Advanced Application in Hybrid Assays, Regulatory Challenges in Mass Spec, Innovation in Small Molecules, Peptides and Oligos).

机构信息

Pfizer, Andover, MA, USA.

Seattle Genetics, Bothell, WA, USA.

出版信息

Bioanalysis. 2021 Feb;13(4):203-238. doi: 10.4155/bio-2020-0324. Epub 2021 Jan 20.

DOI:10.4155/bio-2020-0324
PMID:33470871
Abstract

The 14 edition of the Workshop on Recent Issues in Bioanalysis (14 WRIB) was held virtually on June 15-29, 2020 with an attendance of over 1000 representatives from pharmaceutical/biopharmaceutical companies, biotechnology companies, contract research organizations, and regulatory agencies worldwide. The 14 WRIB included three Main Workshops, seven Specialized Workshops that together spanned 11 days in order to allow exhaustive and thorough coverage of all major issues in bioanalysis, biomarkers, immunogenicity, gene therapy, cell therapy and vaccine. Moreover, a comprehensive vaccine assays track; an enhanced cytometry track and updated Industry/Regulators consensus on BMV of biotherapeutics by Mass Spectrometry (hybrid assays, LCMS and HRMS) were special features in 2020. As in previous years, this year's WRIB continued to gather a wide diversity of international industry opinion leaders and regulatory authority experts working on both small and large molecules to facilitate sharing and discussions focused on improving quality, increasing regulatory compliance and achieving scientific excellence on bioanalytical issues. This 2020 White Paper encompasses recommendations emerging from the extensive discussions held during the workshop and is aimed to provide the Global Bioanalytical Community with key information and practical solutions on topics and issues addressed, in an effort to enable advances in scientific excellence, improved quality and better regulatory compliance. Due to its length, the 2020 edition of this comprehensive White Paper has been divided into three parts for editorial reasons. This publication covers the recommendations on (Part 1) Hybrid Assays, Innovation in Small Molecules, & Regulated Bioanalysis. Part 2A (BAV, PK LBA, Flow Cytometry Validation and Cytometry Innovation), Part 2B (Regulatory Input) and Part 3 (Vaccine, Gene/Cell Therapy, NAb Harmonization and Immunogenicity) are published in volume 13 of Bioanalysis, issues 5, and 6 (2021), respectively.

摘要

第 14 届生物分析最新问题研讨会(14 WRIB)于 2020 年 6 月 15 日至 29 日以虚拟方式举行,来自全球制药/生物制药公司、生物技术公司、合同研究组织和监管机构的代表超过 1000 人出席了会议。第 14 届 WRIB 包括三个主要研讨会和七个专业研讨会,共为期 11 天,以便全面深入地涵盖生物分析、生物标志物、免疫原性、基因治疗、细胞治疗和疫苗所有主要问题。此外,2020 年还特别设立了一个全面的疫苗分析方法学专题、一个强化的细胞分析专题和更新的行业/监管机构对生物疗法生物标志物的共识(通过质谱法的杂交分析、LCMS 和 HRMS)。与前几年一样,今年的 WRIB 继续聚集了广泛的国际行业意见领袖和监管机构专家,他们从事小分子和大分子药物的工作,以促进分享和讨论,重点是提高质量、增加监管合规性并在生物分析问题上实现科学卓越。本白皮书涵盖了研讨会期间广泛讨论中提出的建议,旨在为全球生物分析社区提供有关所讨论主题和问题的关键信息和实用解决方案,努力推动科学卓越、提高质量和更好的监管合规性。由于篇幅较长,出于编辑原因,2020 年版的这份全面白皮书分为三部分。本出版物涵盖了(第 1 部分)杂交分析、小分子创新和监管生物分析方面的建议。第 2 部分 A(BAV、PK LBA、流式细胞术验证和细胞术创新)、第 2 部分 B(监管投入)和第 3 部分(疫苗、基因/细胞治疗、中和抗体分析的协调和免疫原性)分别发表在 Bioanalysis 第 13 卷第 5 期和第 6 期(2021 年)。

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Pharm Res. 2022 Oct;39(10):2541-2554. doi: 10.1007/s11095-022-03371-2. Epub 2022 Aug 19.
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Bioanalytical Methods and Strategic Perspectives Addressing the Rising Complexity of Novel Bioconjugates and Delivery Routes for Biotherapeutics.生物分析方法与战略视角:应对新型生物缀合物和生物治疗药物传递途径日益增加的复杂性。
BioDrugs. 2022 Mar;36(2):181-196. doi: 10.1007/s40259-022-00518-w. Epub 2022 Apr 1.
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Bioanalysis in the Age of New Drug Modalities.新药模式时代的生物分析。
AAPS J. 2021 May 3;23(3):64. doi: 10.1208/s12248-021-00594-w.