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. 2012 Jan 13;74(1):75–85. doi: 10.1111/j.1365-2125.2012.04173.x

Figure 1.

Figure 1

Arithmetic mean plasma concentration–time profiles of linagliptin 5 mg after single oral doses (A) and at steady-state (B), and of CD1790 after single oral doses of linagliptin (C) and at steady-state (D) in healthy subjects (normal hepatic function) and patients with mild, moderate or severe hepatic impairment. (A and C) Normal hepatic function (n = 8) (Inline graphic); Mild hepatic impairment (n = 8) (Inline graphic); Moderate hepatic impairment (n = 9) (Inline graphic); Severe hepatic impairment (n = 8) (Inline graphic); (B and D) Normal hepatic function (n = 8) (Inline graphic); Mild hepatic impairment (n = 8) (Inline graphic); Moderate hepatic impairment (n = 8*) (Inline graphic); Severe hepatic impairment (median prediction) (Inline graphic); Severe hepatic impairment (5th percentile prediction) (Inline graphic); Severe hepatic impairment (95th percentile prediction) (Inline graphic). *Eight patients only completed the multiple dosing period in the moderate impairment group. †Distribution of predicted arithmetic mean steady-state profiles for severe hepatic impairment group (1000 simulated studies with n = 8)