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. 2021 Aug 30;11(5):1763–1776. doi: 10.1007/s13555-021-00596-8

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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. 4 — Deucravacitinib and JAK 1/2/3 inhibitors’ pharmacokinetic parameters and whole blood IC₅₀ values. BID twice daily, C_ave average plasma concentration, C_max maximum plasma concentration, C_min minimum or trough plasma concentration, IC₅₀ half-maximal inhibitory concentration, JAK Janus kinase, QD once daily, TYK2 tyrosine kinase 2