TABLE 4

Pharmacokinetic variables of gemfibrozil and gemfibrozil 1-O-β-glucuronide in nine healthy volunteers after the last dose of 600 mg of gemfibrozil, which was taken 1, 24, 48, or 96 h before time zero (i.e., administration of repaglinide)

Values are mean ± S.D., with the exception of tmax data, which are given as median and range.

VariableTime from the Last Gemfibrozil Dose
1 h24 h48 h96 h
Gemfibrozil
    C0 (μg/ml)17.7 ± 8.50.13 ± 0.060.009 ± 0.007<0.0025
    Cmax (μg/ml)26.2 ± 8.7
    tmax (min)40 (0–80)
    t1/2 (h)1.8 ± 0.33.8 ± 0.97.3 ± 2.4
    AUC0–9 h (μg × h/ml)60.8 ± 19.20.52 ± 0.280.048 ± 0.029<0.023
Gemfibrozil 1-O-β-glucuronide
    C0 (μg/ml)13.8 ± 5.30.18 ± 0.110.008 ± 0.005<0.0025
    Cmax (μg/ml)28.8 ± 7.0
    tmax (min)80 (40–120)
    t1/2 (h)2.0 ± 0.33.7 ± 0.67.8 ± 2.6
    AUC0–9 h (μg × h/ml)105.6 ± 25.40.74 ± 0.430.043 ± 0.023<0.023
  • AUC0–9 h, area under the plasma concentration-time curve from time 0 to 9 h after repaglinide administration, i.e., beginning 1, 24, 48, or 96 h after the last gemfibrozil dose.