Extensive preclinical evaluation of an infliximab biosimilar candidate

Eur J Pharm Sci. 2017 May 1:102:35-45. doi: 10.1016/j.ejps.2017.01.038. Epub 2017 Feb 7.

Abstract

Infliximab is therapeutic monoclonal antibody (mAb) against TNF-α employed in the treatment of immunoinflammatory diseases. The development of biosimilar mAbs is a global strategy to increase drug accessibility and reduce therapy-associated costs. Herein we compared key physicochemical characteristics and biological activities produced by infliximab and infliximab-Probiomed in order to identify functionally relevant differences between the mAbs. Binding of infliximab-Probiomed to TNF-α was specific and had kinetics comparable to that of the reference product. Both mAbs had highly similar neutralizing efficacy in HUVEC cell cultures stimulated with TNF-α. In vitro induction of CDC and ADCC were also similar between the evaluated products. In vivo comparability was assessed using a transgenic mouse model of arthritis that expresses human TNF-α in a 13-week multiple-administration study. Infliximab and infliximab-Probiomed showed comparable efficacy, safety, and pharmacokinetic profiles. Our results indicate that infliximab-Probiomed has highly similar activities to infliximab in preclinical models, warranting a clinical evaluation of its biosimilarity.

Keywords: Biosimilar; Infliximab; Rheumatoid arthritis; TNF-α; Therapeutic mAb; anti-TNF-α.

MeSH terms

  • Animals
  • Antirheumatic Agents* / pharmacokinetics
  • Antirheumatic Agents* / pharmacology
  • Antirheumatic Agents* / therapeutic use
  • Arthritis / drug therapy
  • Arthritis / metabolism
  • Biosimilar Pharmaceuticals* / pharmacokinetics
  • Biosimilar Pharmaceuticals* / pharmacology
  • Biosimilar Pharmaceuticals* / therapeutic use
  • CHO Cells
  • Cells, Cultured
  • Cricetulus
  • Cytokines / genetics
  • Cytokines / metabolism
  • E-Selectin / metabolism
  • HEK293 Cells
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Infliximab* / pharmacokinetics
  • Infliximab* / pharmacology
  • Infliximab* / therapeutic use
  • Intercellular Adhesion Molecule-1 / metabolism
  • Male
  • Mice
  • Mice, Transgenic
  • Vascular Cell Adhesion Molecule-1 / metabolism

Substances

  • Antirheumatic Agents
  • Biosimilar Pharmaceuticals
  • Cytokines
  • E-Selectin
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1
  • Infliximab