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. 2018 Oct 20;35(11):1894–1904. doi: 10.1007/s12325-018-0799-5

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© The Author(s) 2018

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. 5 — DMTs administered during the follow-up period (as percentage of patients) in a patients stable on any IFN beta therapy* at baseline and b patients stable on IM IFN beta-1a therapy at baseline (switch cohort only). DMT disease-modifying therapy, IFN interferon, IM intramuscular. *IFN beta therapies included SC IFN beta-1a, SC IFN beta-1b, and IM IFN beta-1a