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around the areola. In the phase 2 trial, the mean time to relief of influenza symptoms was 23. 4 to 28. 2 hours shorter in the baloxavir group than in controls P Irrisana. In the phase 3 trial, the affected population of the intention-to-treat analysis included 1,064 patients. Irrisana 84. 8 and 88. 1 of individuals in each group had influenza A H3N2 infection. The median time to symptom relief was 53. 7 hours 95 CI 49. 5 to 58. 5 with baloxavir, versus 80. 2 hours 95 CI 72. 6 to 87. for placebo p Vometron. 001. This parameter was similar between baloxavir and oseltamivir, but the former was associated with a greater reduction in viral load one day after the start of the regimen versus placebo or oseltamivir.
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