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. 2008 Apr;65(Suppl 1):60–67. doi: 10.1111/j.1365-2125.2008.03137.x

Table 3.

Summary of maraviroc pharmacokinetic parameters (study 2, cohort 1)

Mean (CV% or SD)
Parameter 3 mg i.v. (n = 8) 10 mg i.v. (n = 8) 30 mg i.v. (n = 8)
AUCt (ng ml−1 h)* 57.6 (15.3%) 201 (12.0%) 670 (12.5%)
AUC (ng ml−1 h)* nc nc 687 (12.0)
Cmax (ng ml−1)* 36.9 (18.6%) 122 (14.6%) 397 (13.8%)
Tmax (h) 0.94 (0.12) 0.94 (0.18) 0.91 (0.19)
t1/2 (h) nc nc 13.2 (2.80)
CL (l h−1) nc nc 44.0 (5.55)
CLR (l h−1) 11.2 (1.52) 10.5 (1.63) 10.2 (1.69)
CLnR (l h−1) nc nc 33.8 (4.67)
Vss (l) nc nc 194 (60.7)
*

Unadjusted geometric means (%CV).

Unadjusted arithmetic means (SD). CV, coefficient of variation; nc, not calculated; SD, standard deviation; Vss, volume of distribution at steady state.

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