Relative Bioavailability of 2 Fixed Dose Combinations of Empagliflozin/Metformin Extended Release (XR) Compared With Single Tablets
Completed · Phase 1
Conditions studied: Healthy
In brief
The purpose of this trial is to demonstrate the relative bioavailability of 2 newly developed fixed dose combinations (FDC) tablets containing empagliflozin \& metformin XR and the single tablets of empagliflozin and metformin XR when administered singularly
Key facts
- Study ID
- NCT02106923
- Run by
- Boehringer Ingelheim
- People needed
- 72
- Starts
- 2014-04-01
- Expected to finish
- 2014-07-01
- Last updated by the study team
- 2017-03-09
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy males or females
- Age 18-50 years (incl.)
- Body Mass Index (BMI) 18.5 to 29.9 kg/m2 (incl.)
- Subjects must be able to understand and comply with study requirements
You may not qualify if…
- Any deviation from healthy condition
Where it is running
- Boehringer Ingelheim Investigational Site — Austin, Texas, United States
Full record on ClinicalTrials.gov
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