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Study aim
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Bioequivalence study of Empagliflozin 10 mg (Tehran Chemie Pharmaceutical Company) versus Jardiance(Boehringer Ingelheim) Tablet after single oral dosing in healthy volunteers
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Design
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Bioequivalence study, with control group, double-blind, randomized, on 24 volunteers, from each volunteer 20 blood samples were taken. Sealed envelope is used for randomization.
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Settings and conduct
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The subject of this biopharmaceutical and pharmacokinetic study is the location of Blood collection center of Tam Pouya Company located in Tehran. The study was blinded to the study participants by removing the drugs from the original package and placing the test and reference drugs in the same package, and the participants were not aware of the type of drug they were taking. The crossover design is such that the Iranian drug will be prescribed to the first group in the first week and to the second group in the second week. Brand medicine, on the contrary, Iranian medicine will be prescribed.
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Participants/Inclusion and exclusion criteria
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Inclusion criteria: general health (liver, heart and kidneys), body mass index (18-28), informed consent, age (50-18) Exclusion criteria: smoking, history of cardiovascular disease, history of liver disease and Renal, alcohol and drug addiction, history of allergy to Empagliflozin
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Intervention groups
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Intervention group: Receives one tablet of test drug (Empagliflozin 10 mg tablet pharmaceutical company Tehran Chemie). Control group: Receives one reference medicine tablet Jardiance 10 mg tablet Boehringer Ingelheim pharmaceuticals)
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Main outcome variables
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Drug concentration in plasma samples