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. 2008 Dec 11;67(2):153–160. doi: 10.1111/j.1365-2125.2008.03297.x

Figure 1.

Figure 1

Schematic representation of the process of selecting starting doses in a first-in-human trial of a MAB. Eff1–3 could be predicted human effects such as biomarkers, toxicological effects, etc. HED, human equivalent no adverse event level dose; RO, receptor occupancy