Pharmacokinetics and tolerability of a single inhaled dose of zanamivir inchildren

Citation
Aw. Peng et al., Pharmacokinetics and tolerability of a single inhaled dose of zanamivir inchildren, CURR THER R, 61(1), 2000, pp. 36-46
Citations number
28
Categorie Soggetti
Pharmacology,"Pharmacology & Toxicology
Journal title
CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL
ISSN journal
0011393X → ACNP
Volume
61
Issue
1
Year of publication
2000
Pages
36 - 46
Database
ISI
SICI code
0011-393X(200001)61:1<36:PATOAS>2.0.ZU;2-D
Abstract
Objective: The purpose of this study was to examine the pharmacokinetics, s afety, and tolerability of zanamivir in children, Background: Zanamivir is a potent inhibitor of viral neuraminidase that is effective against both influenza A and B infections, Methods: A pediatric study was conducted to examine the pharmacokinetics, s afety, and tolerability of zanamivir in children who had signs of respirato ry illness. Twenty-four children aged 3 months to 12 years received zanamiv ir administered as a single, orally inhaled, 10-mg dose either by nebulizer (in patients <5 years of age) or by Diskhaler(R) (in patients greater than or equal to 5 years of age), Serum and urine zanamivir concentrations were analyzed both before dosing and from 0.5 to 8 hours after dosing, Results: The rate and extent of absorption of zanamivir were independent, o f the inhalation formulation or of the patient's age, Median maximum serum concentrations were 47 ng/mL in younger patients (aged greater than or equa l to 3 months to <5 years and greater than or equal to 5 to <9 years) and 4 0 ng/mL in older patients (aged greater than or equal to 9 to less than or equal to 12 years). These maximum concentrations were attained by 1.5 hours after dosing. Median values for area under the curve from 0 time after dos ing to infinite time after dosing were 184 ng.h/mL in patients greater than or equal to 3 months to <5 years of age, 192 ng.h/mL in patients greater t han or equal to 5 to <9 years of age, and 167 ng.h/mL in patients greater t han or equal to 9 to less than or equal to 12 years of age. Less than 8% of the inhaled drug was excreted in urine as unchanged drug These results ind icate a low bioavailability of zanamivir after pulmonary delivery and sugge st that zanamivir is not metabolized in children before excretion, Adverse events observed in this: study were mild and resolved spontaneously, Conclusions: Results of the present study suggest that a 10-mg dose of zana mivir is safe and well tolerated when used in children who have signs and s ymptoms of respiratory illness.