Clinical efficacy of the rituximab biosimilar Acellbia® 600 mg in patients with active rheumatoid arthritis in clinical practice

Objective: to evaluate the clinical efficacy of the rituximab biosimilar Acellbia® at a dose of 600 mg intravenously at a 2-week interval in patients with active rheumatoid arthritis (RA) 12 and 24 weeks after initiation of treatment.Subjects and methods. Examinations were made in 20 active seroposi...

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Bibliographic Details
Main Authors: D. A. Kusevich, A. S. Avdeeva, V. V. Rybakova, N. V. Chichasova, E. L. Nasonov
Format: Article
Language:Russian
Published: IMA PRESS LLC 2019-01-01
Series:Научно-практическая ревматология
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Online Access:https://rsp.mediar-press.net/rsp/article/view/2645
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