TY - JOUR
T1 - Population pharmacokinetic analysis of micafungin in Japanese patients with fungal infections.
AU - Tabata, Kenji
AU - Katashima, Masataka
AU - Kawamura, Akio
AU - Kaibara, Atsunori
AU - Tanigawara, Yusuke
N1 - Funding Information:
Posthoc CL values from the ˆnal model were plotted versus age (Fig. 6A). The body weight-corrected CL show the constant values across the age (Fig. 6B). This observation is supported by the fact that no age-dependence was seen for the weight-corrected posthoc CL value (mLWminWkg).
PY - 2006/8
Y1 - 2006/8
N2 - The object of this analysis was to develop a population pharmacokinetic model of micafungin, a new anti-fungal agent of the echinocandin class, to optimize dosing in Japanese patients with fungal infections. Population pharmacokinetics parameters were determined using NONMEM based on pharmacokinetic data from 198 subjects in seven clinical studies, comprising four phase I, two phase II and one pediatric phase III study. The healthy subjects received intravenous infusion of 2.5-150 mg micafungin. Adult and pediatric patients, age range of 8 month to 15 yeras old, were received 25-150 mg and 1-6 mg/kg daily, respectively. A total of 1825 micafungin plasma samples were available for this analysis. Two-compartment pharmacokinetic model was adopted. The clearance of micafungin was influenced by body weight in children and platelet counts (PLT). However the PLT accounted for less than 20% of the variation of micafungin clearance in Japanese subjects. In conclusions, body weight is the primary covariate factor in pediatric patients. The dose adjustment by body weight would be required only pediatric patients for the micafungin therapy in Japanese patients with fungal infection.
AB - The object of this analysis was to develop a population pharmacokinetic model of micafungin, a new anti-fungal agent of the echinocandin class, to optimize dosing in Japanese patients with fungal infections. Population pharmacokinetics parameters were determined using NONMEM based on pharmacokinetic data from 198 subjects in seven clinical studies, comprising four phase I, two phase II and one pediatric phase III study. The healthy subjects received intravenous infusion of 2.5-150 mg micafungin. Adult and pediatric patients, age range of 8 month to 15 yeras old, were received 25-150 mg and 1-6 mg/kg daily, respectively. A total of 1825 micafungin plasma samples were available for this analysis. Two-compartment pharmacokinetic model was adopted. The clearance of micafungin was influenced by body weight in children and platelet counts (PLT). However the PLT accounted for less than 20% of the variation of micafungin clearance in Japanese subjects. In conclusions, body weight is the primary covariate factor in pediatric patients. The dose adjustment by body weight would be required only pediatric patients for the micafungin therapy in Japanese patients with fungal infection.
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U2 - 10.2133/dmpk.21.324
DO - 10.2133/dmpk.21.324
M3 - Article
C2 - 16946560
AN - SCOPUS:39049193271
SN - 1347-4367
VL - 21
SP - 324
EP - 331
JO - Drug Metabolism And Pharmacokinetics
JF - Drug Metabolism And Pharmacokinetics
IS - 4
ER -