EBF recommendation on practical management of critical reagents for antidrug antibody ligand-binding assays

被引:15
|
作者
Pihl, Susanne [1 ]
van der Strate, Barry W. A. [2 ,9 ]
Golob, Michaela [3 ]
Ryding, Janka [4 ]
Vermet, Laurent [5 ]
Jaitner, Birgit [6 ]
Goodman, Joanne [7 ]
Timmerman, Philip [8 ]
机构
[1] Ascendis Pharma AS, Copenhagen, Denmark
[2] Univ Med Ctr Groningen, Groningen, Netherlands
[3] Nuvisan GmbH, Grafing, Germany
[4] Svar Life Sci Wieslab AB, Malmo, Sweden
[5] Sanofi Res & Dev, Montpellier, France
[6] Novartis Pharma AG, Basel, Switzerland
[7] AstraZeneca, Cambridge, England
[8] European Bioanal Forum, Havenlaan 86c B204, B-1000 Brussels, Belgium
[9] PRA Hlth Sci, Assen, Netherlands
关键词
antidrug antibody assay; critical reagents; major change; minor change; HOST ANTIBODIES; BIOANALYSIS; STABILITY;
D O I
10.4155/bio-2019-0248
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Immunogenicity assays are required to measure antidrug antibodies that are generated against biotherapeutic modalities. As for any ligand-binding assays, critical reagents (CR) play a crucial role in immunogenicity assays, as the robustness and reliability of an assay are defined by the quality and long-term availability of these reagents. The current regulatory guidelines do not provide clear directions on how to implement and verify lot-to-lot changes of CR during an assay life cycle, or the acceptance criteria that should be used when implementing new lots of CR. These aspects were extensively discussed within the European Bioanalysis Forum community. In this paper, CR for immunogenicity assays are identified and the minimum requirements for introducing new lots of CR in immunogenicity assays are described.
引用
收藏
页码:1787 / 1798
页数:12
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