Skip to main content
. 2016 Feb 18;42(1):99–107. doi: 10.1007/s13318-016-0324-7

Table 2.

Comparison of pharmacokinetic parameters of clopidogrel (CLP) and its metabolites according to CYP3A4*1G status. CYP cytochrome P450

Pharmacokinetic parameter wt/wt wt/*1G p
CLP n = 32 n = 6
 AUC0–t (ng·h/mL) 3.88 (2.23–7.80) 4.42 (2.51–6.86) 0.979
 C max (ng/mL) 1.37 (0.61–2.42) 1.60 (1.03–2.09) 0.761
 T max (h) 1.00 (0.50–2.00) 1.00 (0.50–2.00) 0.699
 t 1/2 (h) 1.15 (0.72–2.33) 1.20 (0.76–1.96) 0.816
 Cl (L/h) 15,607 (8657–22,846) 14,365 (8694–26,772) 0.979
 V d (L) 34,652 (13,840–69,963) 28,763 (21,447–35,866) 0.897
CLPM n = 35 n = 9
 AUC0–t (ng·h/mL) 10,137 (6998–12,135) 7712 (7012–8118) 0.282
 C max (ng/mL) 1952 (1449–2802) 2560 (2116–3512) 0.171
 T max (h) 1.00 (0.75–2.00) 1.00 (0.50–2.00) 0.692
 t 1/2 (h) 7.19 (5.13–9.31) 6.55 (3.42–8.56) 0.602
H3 n = 23 n = 6
 AUC0–t (ng·h/mL) 5.69 (3.27–7.69) 5.70 (1.68–10.14) 0.417
 C max (ng/mL) 3.41 (1.97–5.47) 2.07 (1.45–15.55) 0.686
 T max (h) 1.00 (0.50–1.00) 1.00 (0.50–2.00) 0.752
 t 1/2 (h) 0.52 (0.32–0.87) 0.53 (0.37–0.66) 0.976
H4 n = 23 n = 6
 AUC0–t (ng·h/mL) 7.59 (4.73–18.83) 6.52 (2.55–10.01) 0.484
 C max (ng/mL) 5.15 (3.10–10.07) 4.62 (2.15–10.18) 0.979
 T max (h) 1.00 (0.50–1.00) 1.00 (1.00–2.00) 0.286
 t 1/2 (h) 0.65 (0.39–0.99) 0.42 (0.32–1.18) 0.324

Data are presented as medians with interquartile range

AUC 0–t area under time–concentration curve, C max maximum concentration, T max time to reach maximum concentration, k elimination constant, t 1/2 elimination half-life