This trial is conducted in China. The aim of the trial is to investigate safety,pharmacokinetics and pharmacodynamics of ZSP1273 granules
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
72
Oral
The First Affiliated Hospital Of Guangzhou Medical University
Guangzhou, Guangdong, China
Plasma concentrations of ZSP1273
Time frame: DAY1~5
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Time frame: DAY1~29
Time to alleviation of influenza symptoms (duration of influenza)
Time frame: DAY1~29
Percentage of subjects with virus titer detected
Time frame: DAY1~29
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.