Zanamivir for treatment of symptomatic influenza A and B infection in children five to twelve years of age: a randomized controlled trial

Background. Influenza infection rates are higher in children than in other age groups. This study evaluated the efficacy, safety and tolerability of a 5-day course of twice daily inhaled zanamivir, 10 mg, compared with placeb o in the treatment of symptomatic influenza A and B viral infections among children 5 to 12 years of age. Methods. This double blind, randomized, placebo-controlled, parallel group, multicenter study conducted in the Northern Hemisphere during the 1998 and 1999 influenza season enrolled 471 patients with influenza-like symptoms f or less than or equal to 36 h. Patients were randomly assigned to zanamivir (n = 224) or placebo (n = 247). Symptoms were recorded on diary cards twic e daily during treatment, for 9 days after treatment and for 14 additional days (if still reporting moderate/severe cough and/or taking relief medicat ion). Findings. A total of 346 (73%) patients were influenza-positive by culture, serology or polymerase chain reaction (65% influenza A, 35% influenza B). Zanamivir reduced the median time to symptom alleviation by 1.25 days compa red with placebo among patients with confirmed influenza infection (P < 0.0 01), Zanamivir-treated patients returned to normal activities significantly faster and took significantly fewer relief medications than placebo-treate d patients. Zanamivir was well-tolerated, demonstrating adverse event profi les similar to those of placebo and no clinically significant changes in la boratory findings. Viral susceptibility testing revealed no zanamivir-resis tant strains of influenza A or B. Conclusions. Zanamivir was effective in shortening the duration and severit y of influenza symptoms and was well-tolerated among children 5 to 12 years of age.