Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/35986
Title: Efficacy and Safety of the Neuraminidase Inhibitor Zanamivir in the Treatment of Influenzavirus Infections
Authors: Hayden, F. G.
Osterhaus, A. D. M. E.
Treanor, J. J.
Fleming, D. M.
Aoki, F. Y.
Nicholson, Karl G.
Bohnen, A. M.
Hirst, H. M.
Keene, O.
Wightman, K.
First Published: 25-Sep-1997
Publisher: Massachusetts Medical Society
Citation: New England Journal of Medicine 1997; 337:874-880
Abstract: Background The sialic acid analogue zanamivir (GG167) is a selective inhibitor of influenza A and B virus neuraminidases. These viral enzymes are essential for the release of virus from infected cells, and they may also reduce the inactivation of virus by respiratory secretions. When administered experimentally directly to the respiratory tract, zanamivir has potent antiviral effects. We assessed the therapeutic activity of zanamivir in adults with acute influenza. Methods We conducted separate randomized, double-blind studies in 38 centers in North America and 32 centers in Europe during the influenza season of 1994–1995. A total of 417 adults with influenza-like illness of 48 hours’ duration were randomly assigned to one of three treatments: 6.4 mg of zanamivir by intranasal spray plus 10 mg by inhalation, 10 mg of zanamivir by inhalation plus placebo spray, or placebo by both routes. Treatments were selfadministered twice daily for five days. Results Of 262 patients with confirmed influenzavirus infection (63 percent of all patients), the median length of time to the alleviation of all major symptoms was one day shorter (four days vs. five days) in the 88 patients given inhaled and intranasal zanamivir (P0.02) and the 85 patients given inhaled zanamivir alone (P0.05) than in the 89 patients given placebo. Among the infected patients who were febrile at enrollment and among those who began treatment within 30 hours after the onset of symptoms, the median time to the alleviation of major symptoms was four days in both zanamivir groups and seven days in the placebo group (P0.01). Viral titers of nasal washings in the group given inhaled and intranasal zanamivir were significantly lower than those in the placebo group. The topically administered zanamivir was well tolerated. Conclusions In adults with influenza A or B virus infections, direct administration of a selective neuraminidase inhibitor, zanamivir, to the respiratory tract is safe and reduces symptoms if begun early. (N Engl J Med 1997;337:874-80.)
DOI Link: 10.1056/NEJM199709253371302
ISSN: 0028-4793
eISSN: 1533-4406
Links: http://www.nejm.org/doi/full/10.1056/NEJM199709253371302
http://hdl.handle.net/2381/35986
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: Archived with reference to SHERPA/RoMEO and publisher website.
Appears in Collections:Published Articles, Dept. of Infection, Immunity and Inflammation

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