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. 2013 Feb 5;75(3):779–790. doi: 10.1111/j.1365-2125.2012.04386.x

Figure 4.

Figure 4

Pharmacokineticsand pharmacodynamics of GSK2190915 in healthy Japanese subjects. (a) Mean plasma concentration vs. time profiles for GSK2190915 following single dose administration of 10 mg (Inline graphic), 50 mg (Inline graphic), 150 mg (Inline graphic) or 200 mg (Inline graphic) GSK2190915. (B) Median (plus interquartile range) percentage changes from baseline plasma LTB4 following single dose administration of placebo (Inline graphic) or 10 mg (Inline graphic), 50 mg (Inline graphic), 150 mg (Inline graphic) or 200 mg (Inline graphic) GSK2190915. (C) Median (plus interquartile range) of LTE4 excretion in urine as a percentage of the pre‐dose value following single dose administration of placebo (Inline graphic) or 10 mg (Inline graphic), 50 mg (Inline graphic), 150 mg (Inline graphic) or 200 mg (Inline graphic) GSK2190915.