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Study aim
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Bioequivalence study of Dulotegravir 50 mg tablet manufactured by Sobhan Trading group. versus originator brand (TIVICAY® 50 mg ) manufactured by GlaxoSmithKline in fed condition in healthy volunteers.
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Design
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Bioequivalence study, crossover, single-blinded, 24 healthy volunteers. Simple randomization was used for randomization
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Settings and conduct
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The study is a single-blinded (Volunteers), cross-over and feding, and on two series of healthy volunteers. The study will be done in two periods (48h). The interval between these two periods is a week. In the first round of the study, the candidates were divided into two groups the first group received a test tablet and the second group received a brand tablet. 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 (18-28), Informed consent, Age (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 Dulotegravir
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Intervention groups
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Intervention group 1: Tivicay 50mg tablet manufactured by GlaxoSmithKline as a reference Intervention group 2: TIVIMEX 50 mg manufactured by Sobhan trading group as a test
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Main outcome variables
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Maximum drug concentration, Time to reach maximum drug concentration