Clinical Study

A Randomized, Double-Blind Pilot Study of Dose Comparison of Ramosetron to Prevent Chemotherapy-Induced Nausea and Vomiting

Table 2

Pharmacokinetic parameters of ramosetron after a single intravenous injection of 0.3, 0.45, and 0.6 mg of ramosetron.

0.3 mg0.45 mg0.6 mg
( = 17)( = 15)( = 18)

(ng/mL)3.2 ± 1.34.9 ± 3.37.3 ± 9.3
(h)0.670.670.67
AUClast (ng⋅h/mL)17.9 ± 6.925.9 ± 16.035.2 ± 34.8
(h)6.4 ± 2.26.5 ± 3.26.4 ± 1.8
CL (L/h)17.1 ± 6.621.3 ± 13.622.5 ± 11.8
(L)110.6 ± 38.7128.5 ± 60.6142.3 ± 86.6

Data are presented as mean ± standard deviation.
, maximum concentration; /D, maximum concentration/dose; , time to ; AUClast, area under the concentration-time curve of ramosetron from zero to the last measurable concentration; AUClast/D, area under the concentration-time curve of ramosetron from zero to the last measurable concentration/dose; , terminal half-life; CL, clearance; , volume of distribution at steady state.