The purpose of this study is to estimate the absolute oral bioavailability of dapagliflozin.
Study Type
INTERVENTIONAL
Allocation
NA
Masking
NONE
Enrollment
7
Tablet and IV solution, Oral and IV, 10 mg po and 100 µg IV, Single oral dose followed by a single IV dose (IV dose administered at 1h after oral dose), 1 day
Covance Clinical Research Unit, Inc.
Madison, Wisconsin, United States
Absolute oral bioavailability
Time frame: Within the 3 days after study drug administration
Adverse events (AE)
Time frame: Within the 3 days after study drug administration
Vital signs
Time frame: Within the 3 days after study drug administration
Clinical safety labs
Time frame: Within the 3 days after study drug administration
Electrocardiograms (ECGs)
Time frame: Within the 3 days after study drug administration
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