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EBF recommendation for stability testing of anti-drug antibodies; lessons learned from anti-vaccine antibody stability studies
Author(s) -
Susanne Pihl,
Lydia Michaut,
Jenny Hendriks,
Ralf Loebbert,
Janka Ryding,
Martin Nemansky,
Laurent Vermet,
Arjen Companjen
Publication year - 2014
Publication title -
bioanalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.566
H-Index - 58
eISSN - 1757-6199
pISSN - 1757-6180
DOI - 10.4155/bio.14.95
Subject(s) - immunogenicity , bioanalysis , polyclonal antibodies , drug , antibody , stability (learning theory) , medicine , medical physics , computer science , biochemical engineering , risk analysis (engineering) , pharmacology , chemistry , immunology , chromatography , engineering , machine learning
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.

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