This phase 1 study is to evaluate the pharmacokinetics (PK), metabolism, routes and extent of elimination of a single oral dose of 400 mg \[14C\]LX4211 to healthy male subjects
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
8
Lexicon Investigational Site
Madison, Wisconsin, United States
Area Under Curve (AUC)
Time frame: Day 1: predose, 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 8, 12 hours post-dose
Number of subjects experiencing an adverse event
Time frame: Day 1 through discharge
Urinary recovery of radioactivity
Time frame: predose through 24 hours
Fecal recovery of radioactivity
Time frame: predose through 24 hours
Whole blood and plasma concentration of total radioactivity
Time frame: predose, 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 8, 12 hours post-dose
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