This trial is conducted in China. The aim of the trial is to investigate safety and efficacy of ZSP1273 granules
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
119
Oral
Oral
Beijing Children Hospital
Beijing, China
Time to Alleviation of Symptoms
Participants assessed the severity of influenza-associated symptoms
Time frame: DAY1~DAY15
Plasma concentrations of ZSP1273
Time frame: DAY1~5
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Time frame: DAY1~15
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