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Classic and evolving approaches to evaluating cross reactivity of mAb and mAb-like molecules - A survey of industry 2008-2019.
MacLachlan, Timothy K; Price, Shari; Cavagnaro, Joy; Andrews, Laura; Blanset, Diann; Cosenza, Mary Ellen; Dempster, Maggie; Galbreath, Elizabeth; Giusti, Anna Maria; Heinz-Taheny, Kathleen Marie; Fleurance, Renaud; Sutter, Esther; Leach, Michael W.
Affiliation
  • MacLachlan TK; Novartis Institutes for Biomedical Research, Cambridge, MA, 01239, USA. Electronic address: Timothy.maclachlan@novartis.com.
  • Price S; Charles River Laboratories, 15 Worman's Mill Court, Suite I, Frederick, MD, 21701, USA.
  • Cavagnaro J; Access BIO, LC, Boyce, VA, 22620, USA.
  • Andrews L; AbbVie, 100 Research Dr, Worcester, MA, 01520, USA.
  • Blanset D; Boehringer Ingelheim, 900 Ridgebury Road, Ridgefield, CT, 06877, USA.
  • Cosenza ME; MEC Regulatory & Toxicology Consulting, LLC, Moorpark, CA, 93021, USA.
  • Dempster M; GlaxoSmithKline, 1250 South Collegeville Rd, Collegeville, PA, 19426, USA.
  • Galbreath E; Drug Safety Research and Evaluation, Takeda US, Inc., Cambridge, MA, USA.
  • Giusti AM; Roche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Zurich, Switzerland.
  • Heinz-Taheny KM; Toxicology and Pathology, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46285, USA.
  • Fleurance R; UCB BioPharma SRL, B-1420, Braine L'Alleud, Belgium.
  • Sutter E; Novartis Institutes for Biomedical Research, Basel, Switzerland.
  • Leach MW; Drug Safety Research and Development, Pfizer, Inc, 300 Technology Square, Cambridge, MA, 02139, USA.
Regul Toxicol Pharmacol ; 121: 104872, 2021 Apr.
Article in En | MEDLINE | ID: mdl-33485926
ABSTRACT
Monoclonal antibodies (mAbs) and mAb derivatives have become mainstay pharmaceutical modalites. A critical assessment is to ascertain the specificity of these molecules prior to human clinical trials. The primary technique for determining specificity has been the immunohistochemistry (IHC)-based "Tissue Cross-Reactivity" (TCR) assay, where the candidate molecule is applied to > 30 tissues to look for unexpected staining. In the last few years, however, non-IHC array-based platforms have emerged that allow for screening 75-80% of the human membrane proteome, indicating a viable alternative and/or addition to the IHC methods. The preclinical sciences subcommittee of the Biotechnology Innovation Organization (BIO), "BioSafe", conducted a survey of 26 BIO member companies to understand current sponsor experience with the IHC and array techniques. In the last ten years, respondents noted they have conducted more than 650 IHC TCR assays, largely on full length mAbs, with varying impacts on programs. Protein/cell arrays have been utilized by almost half of the companies and sponsors are gaining familiarity and comfort with the platform. Initial experience with recent versions of these arrays has been largely positive. While most sponsors are not prepared to eliminate the IHC TCR assay, growing experience with these alternatives allows them to confidently choose other approaches with or without TCR assays.
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Full text: 1 Database: MEDLINE Main subject: Cross Reactions / Drug Evaluation, Preclinical / Antibodies, Monoclonal Limits: Animals / Humans Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Cross Reactions / Drug Evaluation, Preclinical / Antibodies, Monoclonal Limits: Animals / Humans Language: En Year: 2021 Type: Article