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Pharmacokinetics of a proposed tocilizumab biosimilar (MSB11456) versus US-licensed tocilizumab: results of a randomized, double-blind, single-intravenous dose study in healthy adults.

Monika Tomaszewska-KiecanaMartin UllmannCorinne Petit-FrereJoëlle MonnetChristos DagresAndras Illes
Published in: Expert review of clinical immunology (2023)
Pharmacokinetic similarity of MSB11456 and US-licensed tocilizumab was demonstrated, with comparable immunogenicity and safety profiles, supporting MSB11455 as a biosimilar to US-licensed tocilizumab. The trial is registered at EudraCT, number 2019-003484-22.
Keyphrases
  • rheumatoid arthritis
  • juvenile idiopathic arthritis
  • rheumatoid arthritis patients
  • clinical trial
  • study protocol
  • double blind
  • phase iii
  • phase ii
  • randomized controlled trial
  • high dose
  • systemic lupus erythematosus