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Study aim
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Bioequivalence study of Empagliflozin/ Linagliptin10/5 mg (JARLINO 10/5 mg) manufactured by Faran pharmed versus originator brand GLYXAMBI® Tab 10/5 mg. manufactured by Beohringer Ingelheim Germany in fasting condition in healthy volunteers
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Design
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Bioequivalence study, crossover, single-blinded, on 24 healthy volunteers. Simple randomization will be used for randomization
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Settings and conduct
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The study is a single-blinded (Volunteers), cross-over and fasting, and on two series of healthy volunteers. The study will be done in two 72 our periods. The interval between these two periods is two weeks. In the first round of the study, the candidates will be divided into two groups. The first group will receive a test tablet and the second group will receive a brand tablet. In the second round, the first group will receive a brand tablet and the second group will receive a test tablet. The blood samples are collected immediately before and after drug administration by volunteers. Then, drug extraction is done and samples are ready for analysis. Sampling is performed in Radin laboratory in Tabriz.
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Participants/Inclusion and exclusion criteria
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Inclusion Criteria: General Health (Liver, Heart, and Kidney), Body Mass Index of 18-28, Informed consent, Age of 18-55 years old. Exclusion criteria: Smoking, History of cardiovascular disease, History of liver and kidney disease, Alcohol and drug addiction, History of allergy to Empagliflozin or linagliptin
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Intervention groups
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Intervention group 1: Empagliflozin/ Linagliptin10/5 mg ( GLYXAMBI® Tab 10/5 mg) manufactured by Beohringer Ingelheim Germanyas as reference.
Intervention group 2: Empagliflozin/ Linagliptin10/5 mg ( JARLINO 10/5 mg) manufactured by Faran pharmed Co. as test
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Main outcome variables
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Maximum drug concentration, Time to reach maximum drug concentration