The objectives of this substance balance study in healthy Chinese adult male subjects are to obtain human radioactivity recovery data and major excretion pathways, and to obtain pharmacokinetics of total radioactivity in plasma, and to identify major metabolites in the radiometabolite spectrum. The main questions it aims to answer are: * Quantitative analysis of total fecal and urine radioactivity in healthy subjects after oral administration of \[14C\]ZX-7101A to obtain human radioactive recovery data and main excretion routes. * Pharmacokinetics of total activity in whole blood and plasma, and distribution of total activity in whole blood and plasma are quantitatively analyzed after oral administration of \[14C\]ZX-7101A in healthy subjects. * Quantitative analysis of the radioactive metabolites in plasma, urine and feces of healthy subjects with once \[14C\]ZX-7101A orally administration, identification of the main metabolites of the radioactive metabolites (close to or greater than 10% of the total radioactive AUC in plasma), and determination of the main biotransformation and elimination pathway of ZX-7101A.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
6
a drug to treatment influenza in Chinese adults
The First Affiliated Hospital of Soochow University
Suzhou, Jiangsu, China
Cumulative recovery of total radioactive material in urine and feces
The total radioactivity in excreta of healthy subjects after oral administration of \[14C\]ZX-7101A
Time frame: From 1 days before medication to 22 days after medication
Cmax of total radioactivity in plasma
The peak concentration of ZX-7101A after oral administration of \[14C\]ZX-7101A in healthy subjects
Time frame: From 1 days before medication to 22 days after medication
AUC of total radioactivity in plasma
The area under curve of ZX-7101A after oral administration of \[14C\]ZX-7101A in healthy subjects
Time frame: From 1 days before medication to 22 days after medication
Number of Participants with Treatment-Related Adverse Events as Assessed by CTCAE v5.0
The Treatment-Related Adverse Events of ZX-7101A will be evaluated by the change of vital signs, electrocardiogram (P Wave, QRS Complex, QT Interval), physical examination, and Laboratory test compared with the baseline.
Time frame: From medication to 22 days after medication
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