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Perspective

Waiving in vivo studies for monoclonal antibody biosimilar development: National and global challenges

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Pages 427-435 | Received 06 Nov 2015, Accepted 19 Jan 2016, Published online: 24 Mar 2016

References

  • EU Guideline on Similar Biological Medicinal Products (CHMP/437/04) (http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2009/09/WC500003517.pdf)
  • EU Guideline on similar biological medicinal products containing monoclonal antibodies – nonclinical and clinical issues (EMA/CHMP/BMWP/403543/2010) (http://www.ema.europa.eu/docs/en_GB /document_library/Scientific_guideline/2012/06/WC500128686.pdf)
  • Scientific Considerations in Demonstrating Biosimilarity to a Reference Product (http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM291128.pdf)
  • Bui LA, Hurst S, Finch GL, Ingram B, Jacobs IA, Kirchhoff CF, Ng CK, Ryan AM. Key considerations in the preclinical development of biosimilars. Drug Discovery Today 2015; 20(1): 3-15; PMID:25912284; http://dx.doi.org/10.1016/j.drudis.2015.03.011
  • http://www.ema.europa.eu/docs/en_GB/document_library/Press_release/2013/06/WC500144941.pdf
  • EU Guideline on similar biological medicinal products containing biotechnology-derived proteins as active substance: nonclinical and clinical issues (EMEA/CHMP/BMWP/42832/2005 Rev1). http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2015/01/WC500180219.pdf
  • Martin PL, Bugelski PJ. Concordance of preclinical and clinical pharmacology and toxicology of monoclonal antibodies and fusion proteins: soluble targets. British Journal of Pharmacology 2012 Jun;166 (3):806-22; PMID:22168335; http://dx.doi.org/10.1111/j.1476-5381.2011.01812.x
  • Bugelski PJ, Martin PL. Concordance of preclinical and clinical pharmacology and toxicology of therapeutic monoclonal antibodies and fusion proteins: cell surface targets. British Journal of Pharmacology 2012 Jun;166 (3):823-46; PMID:22168282; http://dx.doi.org/10.1111/j.1476-5381.2011.01811.x
  • van Meer PJ, Kooijman M, van der Laan JW, Moors EH, Schellekens H. The value of non-human primates in the development of monoclonal antibodies. Nature Biotechnology 2013 Oct;31 (10):882-3; PMID:24104750; http://dx.doi.org/10.1038/nbt.2709
  • Bussiere JL. Species selection considerations for preclinical toxicology studies for biotherapeutics. Expert Opinion in Drug Metabolism and Toxicology 2008; 4(7):871-7; PMID:18624676; http://dx.doi.org/10.1517/17425255.4.7.871
  • Chapman K, Pullen N, Graham M, Ragan I. Preclinical safety testing of monoclonal antibodies: the significance of species relevance. Nature Reviews Drug Discovery 2007; 6: 120-126; PMID:17268483; http://dx.doi.org/10.1038/nrd2242
  • Chapman K, Andrews L, Bajramovic JJ, Baldrick P, Black LE, Bowman CJ, Buckley LA, Coney LA, Couch J, Dempster M, et al. The design of chronic toxicology studies of monoclonal antibodies: implications for the reduction in the use of non-human primates. Regulatory Toxicology and Pharmacology 2012; 62 (2): 347-54; PMID:22100994; http://dx.doi.org/10.1016/j.yrtph.2011.10.016
  • Chapman K, Pullen N, Coney L, Dempster M, Andrews L, Bajramovic J, Baldrick P, Buckley L, Jacobs A, Hale G, et al. Preclinical development of monoclonal antibodies. Considerations for the use of non-human primates. mAbs 2009; 1:5, 505-516; PMID:20065651; http://dx.doi.org/10.4161/mabs.1.5.9676
  • ICH S6 (R1). Preclinical safety evaluation of biotechnology-derived pharmaceuticals. In: International Conference on Harmonisation (ICH). Topic S6 (R1). June 2011.
  • Quality Considerations in Demonstrating Biosimilarity of a Therapeutic Protein Product to a Reference Product (http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM291134.pdf)
  • Krishnan A, Mody R, Malhotra, H. Global regulatory landscape of biosimilars: emerging and established market perspectives. Biosimilars 2015; 5: 19-32; http://dx.doi.org/10.2147/BS.S44052
  • van Aerts LAGJM, Smet K, Reichmann G, van der Laan JW, Schneider CK. Biosimilars entering the clinic without animal studies: A paradigm shift in the European Union. mAbs 2014; 6:5, 1155-1162; PMID:25517301; http://dx.doi.org/10.4161/mabs.29848
  • Van Meer PJK, Ebbers HC, Kooijman M, Gispen-de Wied CC, Silva-Lima B, Moors EHM, Schellekens H. Contribution of animal studies to evaluate the similarity of biosimilars to reference products. Drug Discovery Today 2014; 120(4): 483-490; PMID:25463036; http://dx.doi.org/10.1016/j.drudis
  • European Medicines Agency. Committee for Medicinal Products for Human Use (CHMP) EMA/CHMP/589317/2013. European Public Assessment Report Remsima International non-proprietary name: Infliximab
  • Heim HK. Geneva, April 27 (2015): Session 3: Review of the current WHO SBPs Guidelines: Regulatory perspectives, Federal Institute for Drugs and Medical Devices (BfArM)
  • Leach MW. Regulatory forum opinion piece: differences between protein-based biologic products (biotherapeutics) and chemical entities (small molecules) of relevance to the toxicologic pathologist. Toxicological Pathology 2013; 41(1):128-36; PMID:22744226; http://dx.doi.org/10.1177/0192623312451371
  • Schiestl M, Stangler T, Torella C, Čepeljnik T, Toll H, Grau R. Acceptable Changes in Quality Attributes of Glycosylated Biopharmaceuticals. Nature Biotechnology 2011; 29: 310-312; PMID:21478841; http://dx.doi.org/10.1038/nbt.1839
  • Abdiche YN, Yeung YA, Chaparro-Riggers J, Barman I, Strop P, Chin SM, Pham A, Bolton G, McDonough D, Lindquist K, et al. The neonatal Fc receptor (FcRn) binds independently to both sites of the IgG homodimer with identical affinity. mAbs 2015; 7(2):331-43; PMID:25658443; http://dx.doi.org/10.1080/19420862.2015.1008353
  • Kliwinski C, Cooper PR, Perkinson R, Mabus JR, Tam SH, Wilkinson TM, Giles-Komar J, Scallon B, Powers GD, Hornby PJ. Contribution of FcRn binding to intestinal uptake of IgG in suckling rat pups and human FcRn-transgenic mice. Am J Physiol Gastrointest Liver Physiol 2013; 304(3):262-70; PMID:23220220; http://dx.doi.org/10.1152/ajpgi.00340.2012
  • Ober RJ, Radu CG, Ghetie V, Ward ES. Differences in promiscuity for antibody-FcRn interactions across species: implications for therapeutic antibodies. Int Immunol 2001; 13(12):1551-9; PMID:11717196; http://dx.doi.org/10.1093/intimm/13.12.1551
  • Andersen JT, Daba MB, Berntzen G, Michaelsen TE, Sandlie I. Cross-species binding analyses of mouse and human neonatal Fc receptor show dramatic differences in immunoglobulin G and albumin binding. J Biol Chem. 2010; 12; 285(7):4826-36; PMID:20018855; http://dx.doi.org/10.1074/jbc.M109.081828
  • Ryan AM, Sokolowski SA, Ng C-K, Shirai N, Collinge M, Shen AC, Arrington J, Radi Z, Cummings TR, Ploch SA, et al. Comparative nonclinical assessments of the proposed biosimilar PF-05280586 and rituximab (MabThera®). Toxicological Pathology 2014; 42:1069-1081; PMID:24604381; http://dx.doi.org/10.1177/0192623313520351
  • Hurst S, Ryan AM, Ng C-K, McNally JM, Lorello LG, Finch GL, Leach MW, Ploch SA, Fohey JA, Smolarek TA. Comparative nonclinical assessments of the proposed biosimilar PF05280014 and trastuzumab (Herceptin®). BioDrugs 2014; 28:451-459; PMID:25001079; http://dx.doi.org/10.1007/s40259-014-0103-4
  • Derzi M, Ripp SL, Ng C-K, Shoieb AM, Finch GL, Lorello L, Leach MW. Comparative nonclinical assessments of the potential biosimilar PF-06410293 and adalimumab. SOT Annual Meeting, Phoenix, Arizona, March 24–27 2014
  • Johnson TR, Derzi M, Bolt M, Ng C-K, Kirchhoff CF, Lorello L, McNally J, Leach MW, Smolarek TA. Comparative Nonclinical Assessments of Marketed Infliximab Presentations (Remicade®) and the Potential Biosimilar PF06438179. 14th Annual American Association of Pharmaceutical Scientists (AAPS) National Biotechnology Conference, San Diego, California, May 19–21. 2014
  • Ripp SL, Bolt M, Derzi M, Finch G, Hurst S, Johnson TR, Leach MW, Smolarek TA. A fit-for-purpose approach to nonclinical assessments for adalimumab and infliximab biosimilar development. 19th North American Regional ISSX Meeting and 29th JSSX Annual Meeting, San Francisco, California, October 19–23 2014.
  • Peraza M, Shiue M, Phenix S, Rule K, Finch G, Thibault S, Leach MW. Comparative nonclinical assessment of the potential biosimilar PF-06439535 and bevacizumab. In: 2015 Annual Meeting Abstract Supplement, Society of Toxicology, 2015, Abstract no. 603.