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. 2023 Jun 15;13(7):1517–1534. doi: 10.1007/s13555-023-00942-y

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© The Author(s) 2023

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. 2 — Time course response for EASI clinical outcomes. Percentage of patients (%) achieving EASI-75 (A), EASI-90 (B), EASI-50 (C), and EASI percentage change from baseline (D) through 52 weeks. Missing data due to lack of efficacy were imputed with non-responder imputation. Other missing data were imputed with multiple imputation. Abbreviations: EASI Eczema Area and Severity Index, EASI-50 50% reduction in EASI, EASI-75 75% reduction in EASI, EASI-90 90% reduction in EASI, LEBRI lebrikizumab, Q2W every 2 weeks