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BMJ 2004;328:523 (28 February), doi:10.1136/bmj.328.7438.523-a
| The first 150 words of the full text of this article appear below. |
EDITORIn response to Symmonds et al,1 F Hoffmann-La Roche would like to clarify that data from studies WV15759/WV15871 were made available to the National Institute for Clinical Excellence.
These were double blind, placebo controlled trials, conducted in children aged 6 or older and 12 or younger, to investigate the efficacy and tolerability of oseltamivir in the treatment of influenza among asthmatic children. Of the 355 children randomised to treatment, 170 received oseltamivir 2 mg/kg and 164 received placebo. Of these children, 179 had laboratory confirmed influenza infection, which represented only 70% of the planned recruitment target. This precluded any statistical demonstration of the primary efficacy end point "time to freedom from illness" (incorporating resolution of symptoms and a return to normal activity).
Among the outcomes of this study, a positive effect on forced expiratory volume in one second in the oseltamivir group was seen, an observation that is
Zoya Panahloo, senior medical adviser
United Kingdom F Hoffmann La Roche, Welwyn Garden City, Hertfordshire AL7 3AY zoya.panahloo@roche.com
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