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Antimicrobial Agents and Chemotherapy, July 2000, p. 1974-1976, Vol. 44, No. 7
Clinical Pharmacology Department, Glaxo
Wellcome Inc., Research Triangle Park, North Carolina
27709,1 and Glaxo Wellcome
S.p.A., Medicine Research Centre, Verona, Italy2
Received 7 October 1999/Returned for modification 23 January
2000/Accepted 5 April 2000
In a single-center, randomized study, zanamivir (Relenza)
concentrations in induced sputum samples and nasal washings of healthy adults following oral inhalation were measured. Concentrations in
sputum exceeded the median viral neuraminidase 50% inhibitory concentration at 6, 12, and 24 h, and those in nasal washings did
so at 6 and 12 h. There were no zanamivir-related adverse events
or laboratory abnormalities.
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Direct Measurement of the Anti-Influenza Agent
Zanamivir in the Respiratory Tract following Inhalation
*
Corresponding author. Mailing address: Clinical
Pharmacology Department, Glaxo Wellcome Inc., 5 Moore Dr., Research
Triangle Park, NC 27709. Phone: (919) 483-5445. Fax: (919) 483-6380. E-mail: ap4872{at}glaxowellcome.com.
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