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Evaluation of efficacy and comparative frequency of adverse events in patients with ulcerative colitis receiving the original infliximab and its biosimilar. One year of observation
Knyazev O.V., Shkurko T.V., Kagramanova A.V., Lishchinskaya A.A., Zvyaglova M.Y., Korneeva I.A., Babayan A.F., Parfenov A.I.
The role of laboratory biomarkers in monitoring of rituximab biosimilar therapy (Acellbia, “BIOCAD”) in patients with rheumatoid arthritis
Avdeeva A.S., Cherkasova M.V., Kusevich D.A., Rybakova V.V., Artyuhov A.S., Dashinimaev E.B., Chichasova N.V., Nasonov E.L.
Results of non-medical switching from original infliximab to its Russian biosimilar in patients with ulcerative colitis
Timanovskaia M.I., Knyzev O.V., Parfenov A.I.
The efficacy and safety of eculizumab biosimilar in patients with paroxysmal nocturnal hemoglobinuria. Results of a phase III randomized open-label comparative clinical trial
Kulagin A.D., Bakirov B.A., Davydkin I.L., Elykomov I.V., Konstantinova T.S., Korobkin A.V., Kosinova M.V., Mazurov V.I., Minaeva N.V., Proidakov A.V., Ptushkin V.V., Shatokhin Y.V., Lin'kova Y.N., Zinkina-Orikhan A.V., Morozova M.A.
Loss of response and frequency of adverse events in patients with ulcerative colitis and Crohn’s disease when switching from the original infliximab to its biosimilars
Knyazev O.V., Zvyaglova M.Y., Kagramanova A.V., Li I.A., Sabelnikova E.A., Lishchinskaya A.A., Kulakov D.S., Parfenov A.I.
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