Standard analyses and reporting of clinical and virological endpoints in early-phase trials of dengue therapeutics.
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*Comparisons of laboratory and virological features between study groups should be adjusted for the baseline value, the day of illness on admission, and serotype/serology (for virological features) to maximize power.aAUC calculated based on the trapezoidal rule with values below the limit of detection replaced by half of the detection limit.
创建时间：
2015-12-02
