This trial is conducted in China. This is a multi-center, randomized, double-blind, placebo-controlled clinical trial to assess the efficacy and safety of ZSP1273 in the treatment of Acute Uncomplicated influenza A in adolescents.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
157
Ruijin Hospital
Shanghai, China
Time to Alleviation of Symptoms
Participants assessed the severity of seven influenza-associated symptoms (cough, sore throat, headache, nasal congestion, feverishness or chills, muscle or joint pain, and fatigue) on a 4-point scale (with 0 indicating no symptoms, 1 mild symptoms, 2 moderate symptoms, and 3 severe symptoms).
Time frame: DAY1~DAY15
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Time frame: DAY1~DAY15
Plasma concentrations of ZSP1273
Time frame: DAY1~DAY15
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