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. 2011 Sep;55(9):4386–4393. doi: 10.1128/AAC.00832-10

Table 3.

Plasma pharmacokinetics of finafloxacin in six healthy volunteers per dose after multiple-dose administration (part B)a

Dose (mg) Day no. Cmax (mg/liter) Cmax,norm [(mg/liter)/mg] AUC24h (h · mg/liter) AUC24h,norm [(h · mg/liter)/mg] tmax (h) t1/2 (h) CL/F (liters/h) Vz/F (liters)
150 1 1.69 ± 0.38 0.011 3.76 ± 0.82 0.025 0.50
150 7 1.50 ± 0.52 0.010 4.01 ± 0.64 0.027 0.50 5.3 ± 0.6 37.4 ± 5.8 282 ± 25
300 1 2.96 ± 0.88 0.0099 8.75 ± 3.50 0.029 1.50
300 7 4.15 ± 2.11 0.014 9.09 ± 3.83 0.030 0.63 6.5 ± 2.5 37.4 ± 17.5 337 ± 155
600 1 7.67 ± 3.42 0.013 18.7 ± 7.63 0.031 0.75
600 7 6.76 ± 2.20 0.011 19.2 ± 6.40 0.032 0.88 8.8 ± 3.1 32.5 ± 10.2 409 ± 175
800 1 8.68 ± 1.96 0.011 20.8 ± 7.42 0.026 0.75
800 7 8.95 ± 3.11 0.011 26.1 ± 8.60 0.033 0.88 14.0 ± 5.5 31.6 ± 10.6 659 ± 467
a

Where indicated, values are means ± standard deviations. AUC24h, area under the plasma concentration-time curve to 24 h after dosing. For the explanation of other symbols, see the footnote to Table 2.