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. 2021 Nov 22;9(1):175–189. doi: 10.1007/s40744-021-00396-8

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© The Author(s) 2021

Open Access This 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. 1 — Disposition flow chart of the study population. A total of 905 patients were screened for the study, and 566 eligible patients were randomized into a GB242 group (n = 283) or an infliximab reference product (INF) group (n = 283) to receive 3 mg/kg of GB242 or INF, respectively, coadministered with methotrexate (MTX) and folic acid. The full analysis set (FAS) for GB242 is n = 283 and infliximab reference product (INF) n = 283. The per-protocol set (PPS) for GB242 is n = 237 and INF n = 233