This single-center, open-label, non-randomized study aims to evaluate the pharmacokinetics, mass balance, and metabolic pathways of WX-081 (Sudapyridine) following a single oral dose of \[U-14C\] WX-081 in healthy Chinese male volunteers. A total of 6-10 subjects will be enrolled to obtain complete samples and data from at least six participants. Biological samples, including blood, plasma, urine, and feces, will be collected over a specified time period. The study will assess pharmacokinetic parameters, excretion pathways, and identify major metabolites contributing to over 10% of plasma exposure.
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Cumulative Excretion Rate of Total Radioactivity in Urine
Timeframe: Up to Day 51 post-dose.
Cumulative Excretion Rate of Total Radioactivity in Feces
Timeframe: Up to Day 51 post-dose.