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. 2010 Aug 16;54(11):4568–4574. doi: 10.1128/AAC.00474-10

TABLE 3.

Time to alleviation of symptoms (intent-to-treat infected population)

Population Parameter Value
Peramivir
Placebo
300 mg 600 mg
Overall n 99 97 100
Median (h) (95% CI) 59.1 (50.9-72.4) 59.9 (54.4-68.1) 81.8 (68.0-101.5)
Hazard ratioa (95% CI) 0.681 (0.511-0.909) 0.666 (0.499-0.890)
Adjusted P valueb 0.0092 0.0092
Influenza virus subtype
    A/H1 n 74 69 72
Median (h) 52.5 62.6 81.4
Hazard ratio 0.779 0.899
Adjusted P value 0.1458 0.5384
    A/H3 n 21 25 24
Median (h) 76.1 50.5 81.0
Hazard ratio 0.542 0.326
Adjusted P value 0.0556 0.0008
Symptom duration before study
    0-24 h n 59 51 48
Median (h) 57.2 56.1 86.7
Hazard ratio 0.653 0.663
Adjusted P value 0.0516 0.0516
    24-48 h n 40 46 52
Median (h) 69.1 64.7 70.8
Hazard ratio 0.708 0.694
Adjusted P value 0.1118 0.1118
a

Hazard ratios compared to the placebo group were estimated using Cox proportional-hazards modeling, adjusted for current smoking behavior and composite symptom scores at baseline.

b

P values for comparisons between peramivir and placebo were adjusted using the Hochberg method for multiple comparisons.