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. 2020 Oct 29;34(6):809–823. doi: 10.1007/s40259-020-00447-6

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

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Fig. 3 — Proportion of patients achieving EULAR response and proportion of patients with EULAR and Boolean remission over time (SP2 PPS). a EULAR good/moderate responses up to Week 48. b EULAR and Boolean remission up to Week 48. Dotted lines indicate the treatment switch from ref-ADL group to SDZ-ADL group. EULAR European League Against Rheumatism, ref-ADL reference adalimumab, SDZ-ADL Sandoz biosimilar adalimumab, SP2 PPS study period 2 per protocol set, Wk week