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. 2016 Jan 20;10:357–370. doi: 10.2147/DDDT.S95934

Table 2.

Pharmacokinetic properties of nemonoxacin in 12 healthy Chinese volunteers after a single oral dose of 500 mg of nemonoxacin alone or with cimetidine

Parameters Nemonoxacin alone (Treatment C) Nemonoxacin with cimetidine (Treatment D) Geometric mean ratio (D:C)a
AUC0−t, h·μg/mL 50.8 (8.9) 55.3 (9.6) 1.08 (1.04–1.13)
AUC0−∞, h·μg/mL 51.2 (9.0) 56.0 (9.8) 1.09 (1.04–1.14)
Cmax, μg/mL 7.20 (1.12) 6.90 (1.26) 0.95 (0.86–1.04)
tmax, h 1 (1–1.5)b 1.5 (0.67–2.5)b
t1/2, h 13.7 (0.8) 13.8 (1.9)
MRT, h 9.74 (1.29) 11.5 (1.6)
CL/F, L/h 10.0 (1.6) 9.21 (1.73)
Vz/F, L 199 (37) 183 (40)
Fe, % 62.5 (7.9) 59.2 (9.9) 0.94 (0.87–1.02)
CLr, L/h 6.32 (1.33) 5.48 (1.24) 0.87 (0.78–0.96)

Notes: Data are mean (standard deviation), except

a

point estimates (90% confidence intervals) and

b

medians (ranges). The dash indicates no data available.

Abbreviations: AUC0−∞, area under the plasma concentration–time curve from time 0 to infinity; AUC0−t, area under the plasma concentration time curve from time 0 to the last time point; Cmax, maximum concentration; CL/F, oral clearance; CLr, renal clearance; Fe, percentage of the administered dose recovered in the urine; MRT, mean residence time; t1/2, terminal elimination half-life; tmax, time to reach Cmax; Vz/F, terminal volume of distribution without correction for bioavailability.