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. 2024 Feb 8;3(2):166–185. doi: 10.1038/s44161-023-00418-4

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© The Author(s) 2024

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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Extended Data Fig. 1 — Mean blood loss as a function of (a) dose- and (b) plasma concentration of FVIIa following administration of FVIIa (n = 3–10, dark squares) or FVIIa coformulated with biAb0097 (1:1 mol/mol) (n = 6, red circles) in the tail vein transection model in HA mice carrying the human TLT-1 receptor. Data are mean blood loss ± s.d. FVIIa, activated factor VII; Hb, haemoglobin.

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