Table 6.
Parameter | Odds Ratio | 95% CI | P Value |
---|---|---|---|
Sex (male to female) | 0.474 | .122–1.838 | .2804 |
Baseline body weight (by 1 kg) | 0.970 | .899–1.046 | .4299 |
Baseline sum of symptom scores (by 1 score) | 0.765 | .405–1.445 | .4095 |
Baseline body temperature (by 1°C) | 0.927 | .323–2.662 | .8886 |
Baseline virus-specific HAI antibody titer (≥40 to <40) | 0.276 | .078–0.982 | .0467 |
Baseline influenza virus titer (by 1.0 log10TCID50/mL) | 0.917 | .589–1.429 | .7017 |
Time to treatment from influenza onset (by 12 hours)a | 0.428 | .145–1.265 | .1249 |
Meal before administration on day of dosing (yes to no) | 1.109 | .276–4.450 | .8838 |
Patients with A(H3N2) virus who had paired-sequencing data available and had baseline characteristic data for potential risk factor were included in this analysis (N = 67). Abbreviations: CI, confidence interval; HAI, hemaggulutinin inhibition; PA/I38T, isoleucine substituted by threonine at position 38 of virus polymerase acidic protein; PA/I38M, isoleucine substituted by methionine at position 38 of virus polymerase acidic protein; TCID50, 50% tissue culture infective dose.
aTreated as ordered category of 4 levels.