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. 2004 Apr;57(4):412–415. doi: 10.1111/j.1365-2125.2003.02043.x

Table 2.

Pharmacokinetic parameters for OR-1855 and OR-1896 after an intravenous infusion of levosimendan for 7 days (mean ± SD)

OR-1855 OR-1896
0.05 µg kg−1 min−1 (n = 12) 0.1 µg kg−1 min−1 (n = 12) P value (95% CI) 0.05 µg kg−1 min−1 (n = 12) 0.1 µg kg−1 min−1 (n = 12) P value (95% CI)
Cmax (ng ml−1) 7.8 ± 5.1 18.1 ± 11.2 0.009  (−17.8, −2.9) 9.9 ± 4.7 17.1 ± 9.8 0.030  (−13.7, −0.76)
tmax (h)* 168 (144–314) 170 (144–216) 0.301  (−23.4, 57.6) 180 (144–264) 170 (144–264) 0.873  (−24.4, 28.6)
AUC(0,last)  (ng ml−1 h) 1570 ± 1220 3560 ± 2130 0.011  (−3477, −501) 2120 ± 1260 3450 ± 2050 0.070  (−2770, 118.3)
AUC(0,∞)  (ng ml−1 h) 1650 ± 1260 3950 ± 2420 0.015  (−4085, −505) 2370 ± 1820 3890 ± 2540 0.107  (−3388, 356.8)
t1/2 (h) 72.6 ± 17.8 78.4 ± 27.8 0.579  (−27.4, 15.8) 81.3 ± 37.1 81.2 ± 27.5 0.992  (−27.5, 27.7)
*

median (range). Cmax peak concentration, tmax time to peak concentration, AUC(0,last) area under the curve to the last measured concentration, AUC(0,∞) area under the curve to infinity, t1/2 half-life, 95% CI 95% confidence intervals on the differences.