A Phase 1, Open-label Study of the absorption, metabolism, and excretion of a single oral dose of \[14C\]EDP-305 in healthy male subjects.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
8
\[14C\]EDP-305
Covance Clinical Research Unit
Madison, Wisconsin, United States
Cmax of EDP-305 in plasma
Time frame: Up to 9 days
AUC of EDP-305 in plasma
Time frame: Up to 9 days
AUC-inf in plasma
Time frame: Up to 9 days
Amount excreted in urine (Aeu)
Time frame: Up to 9 days
Amount excreted in feces (Aef)
Time frame: Up to 9 days
Safety measured by adverse events
Time frame: Up to 9 days
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