Investigating the in vivo bioequivalence of Empagliflozin /Metformin tablet
Not Applicable
Recruiting
- Conditions
- In the present study, the products will be administered to healthy volunteers..
- Registration Number
- IRCT20210519051345N31
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
General Health (in terms of Liver, Heart and Kidney)
Age between 18 to 59 years
Being male
Exclusion Criteria
Smoking
History of cardiovascular disease, liver and kidney disease
Alcohol and drug addiction
History of drug allergy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Plasma concentration of drug. Timepoint: At intervals between half and 72 hours after drug administration. Method of measurement: HPLC (High performance liquid chromatography).
- Secondary Outcome Measures
Name Time Method