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. 2024 Oct 17;15:1414059. doi: 10.3389/fphar.2024.1414059

TABLE 3.

Ezetimibe pharmacokinetic parameters based on sex, biogeographical origin, clinical trial and co-administration of drugs.

N AUC72h/DW (h a ng a kg/mL a mg) Cmax/DW (ng a kg/mL a mg) tmax (h)
Sex
Men 51 702.49 (263.96) 33.24 (14.65) 5.50 (1.25–6.50)
Women 45 750.95 (305.26) 37.07 (20.93) 5.50 (1.50–6.00)
Biogeographical Origin
European 80 737.55 (289.10) 35.84 (18.83) 5.50 (1.50–6.00)
Latin-American 13 639.96 (232.90) 31.03 (12.67) 6.00 (0.50–10.25)
Other b 3 765.45 (370.58) 31.01 (7.51) 1.50 (1.50–2.50) a
Clinical Trial
A 33 737.17 (316.01) 32.50 (17.13) 6.00 (1.50–6.50)
B 11 743.27 (320.04) 31.62 (7.98) 6.00 (1.50–6.50)
C 30 666.81 (252.05) 36.24 (17.44) 2.50 (1.00–6.00)
D 22 777.86 (258.77) 38.91 (22.68) 5.50 (1.69–6.13)
Co-administration of drugs
Ezetimibe 44 738.69 (313.28) 32.28 (15.28) 6.00 (1.50–6.50)
Ezetimibe/Simvastatin 52 713.80 (258.39) 37.37 (19.66) 3.00 (1.25–6.00)

Data are shown as mean (standard deviation) for normal distributions and median (Q25-Q75) for non-normal distributions. AUC: area under the curve. DW: dose/weight ratio. Cmax: maximum concentration. Tmax: time to Cmax.

a

It is not possible to generate quartiles, therefore, the range of the data is shown for this result.

b

Other: one volunteer self-reported as Near Eastern and two as East Asian.