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. 2022 Dec 1;28(12):2633–2645. doi: 10.1038/s41591-022-02059-9

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — a, Table summarizing the adverse events (AEs) that occurred at least twice, reported per treatment arm and not showing clear trends in safety. b, Table reporting all of the serious adverse events (SAEs), also not showing safety trends, and with none of them suspected to be related to LNA043. Cohorts 1 and 4–6 are not included as there were no SAEs in these cohorts; however, the final column includes these participants in the total.