EBF recommendation for stability testing of anti-drug antibodies; lessons learned from anti-vaccine antibody stability studies

被引:13
|
作者
Pihl, Susanne [1 ]
Michaut, Lydia [2 ]
Hendriks, Jenny [3 ]
Loebbert, Ralf [4 ]
Ryding, Janka [5 ]
Nemansky, Martin [6 ]
Vermet, Laurent [7 ]
Companjen, Arjen [3 ]
机构
[1] H Lundbeck & Co AS, Drug Dev ADME, Dept Bioanal, DK-2500 Valby, Denmark
[2] DMPK Biol, Novartis Inst Biomed Res, Bioanalyt, CH-4057 Basel, Switzerland
[3] Crucell Holland BV, NL-2301 CA Leiden, Netherlands
[4] AbbVie Deutschland GmbH & Co KG, DMPK BA, Dev Sci, Ludwigshafen, Germany
[5] Ferring Pharmaceut AS, Bioanal, Int Pharma Sci Ctr, DK-2300 Copenhagen S, Denmark
[6] PRA, Bioanalyt Lab, NL-9405 BJ Assen, Netherlands
[7] Sanofi Res & Dev, Drug Safety Anim Res, Biomarkers & Biol Assays, Montpellier, France
关键词
BIOTECHNOLOGY PRODUCTS; HOST ANTIBODIES;
D O I
10.4155/bio.14.95
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Long- and short-term stability testing of the analyte is one of the key parameters in bioanalytical method validation in support of pharmacokinetics. However, for immunogenicity testing, the scientific rationale for long- and short-term stability testing on quality control samples most often spiked with polyclonal antibody raised in a different species should be questioned. Therefore, the European Bioanalysis Forum (EBF) formed a Topic Team to discuss the scientific rationale for stability testing of anti-drug antibodies (ADAs). A review of EBF member companies' experience on ADA stability and on anti-vaccine antibodies from vaccine projects was the basis of this discussion. EBF recommends to perform short-term stability testing of the positive control, but not to perform long-term stability testing of ADAs in nonclinical and clinical studies.
引用
收藏
页码:1409 / 1413
页数:5
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