A review of the totality of evidence in the development of ABP 798, a rituximab biosimilar

Immunotherapy. 2022 Jun;14(9):727-740. doi: 10.2217/imt-2022-0024. Epub 2022 May 11.

Abstract

ABP 798 (RIABNI™) is a biosimilar to rituximab reference product (RP), a monoclonal antibody that targets CD20. Approval of ABP 798 was based on the totality of evidence generated using a stepwise approach which began by showing that it is structurally and functionally similar to rituximab RP. This analytical assessment was followed by a demonstration of pharmacokinetic/pharmacodynamic similarity in patients with rheumatoid arthritis. Comparative clinical efficacy and safety of ABP 798 with rituximab RP was demonstrated as a final step in patients with non-Hodgkin lymphoma and in those with rheumatoid arthritis. Overall, the totality of evidence supported the conclusion that ABP 798 is highly similar to rituximab RP and provided scientific justification for extrapolation to other approved indications of rituximab RP.

Keywords: ABP 798; biologics; biosimilars; non-Hodgkin lymphoma; rheumatoid arthritis; rituximab.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal
  • Arthritis, Rheumatoid* / drug therapy
  • Biosimilar Pharmaceuticals* / pharmacology
  • Biosimilar Pharmaceuticals* / therapeutic use
  • Humans
  • Rituximab / pharmacology
  • Rituximab / therapeutic use
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Biosimilar Pharmaceuticals
  • Rituximab