The purpose of this study is to estimate the absolute oral bioavailability of dapagliflozin.
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Full eligibility criteria for NCT00908271
Ages eligible for Study
18 Years to 45 Years
Genders eligible for Study
Accepts Healthy Volunteers
Healthy male subjects (ages 18 to 45) as determined by medical history, physical examination, 12-lead electrocardiogram (ECG), and clinical laboratory evaluations will be eligible to participate in the study
Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, ECG or clinical laboratory determinations
Participation in a radiolabeled investigational study drug trial within 12 months prior to admission to the clinical facility
Exposure to significant radiation within 12 months prior to admission to the clinical facility
All locations for NCT00908271
United States (1)
Covance Clinical Research Unit, Inc.
Madison, Wisconsin, United States, 53704
View full eligibility
Tris trial is registered with FDA with number: NCT00908271. The sponsor of the trial is AstraZeneca and it is looking for 7 volunteers for the current phase.
Official trial title: Study of the Absolute Oral Bioavailability of Dapagliflozin in Healthy Subjects
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