The purpose of the study is to learn more about how esreboxetine is handled by the body i.e. the absorption, metabolism and excretion of esreboxetine.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
4
Single oral dose of 6mg esreboxetine in solution containing approximately 100uCi \[14C\]-esreboxetine
Pfizer Investigational Site
Tacoma, Washington, United States
Cumulative excretion of radioactivity in urine and and faeces as a percentage of the total radioactive dose administered over time. Collection of plasma, urine and faeces for the assessment of parent drug and metabolites of esreboxetine where possible
Time frame: Approx 10 days
Pharmacokinetic parameters of esreboxetine and identification and abundance of metabolites in plasma, urine and faeces if possible
Time frame: Approx 10 days
Clinical safety data
Time frame: Approx 10 days
Pharmacokinetic parameters of plasma esreboxetine metabolites if possible
Time frame: Approx 10 days
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