-
Study aim
-
Bioequivalence study of Tablet Ibuprofen ER 800 mg kimiara Heram pharmaceutical company versus Brufen® Retard Abbott/UK pharmaceutical company Tablet after single oral dosing in healthy volunteers
-
Design
-
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.
-
Settings and conduct
-
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.
-
Participants/Inclusion and exclusion criteria
-
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 Ibuprofen
-
Intervention groups
-
Intervention group: Receives one tablet of test drug (Ibuprofen ER 800 mg kimiara Heram Pharmaceutical Company). Control group: Receives one reference medicine tablet (Brufen® Retard 800 Abbott/UK corporation).
-
Main outcome variables
-
Determination of blood concentration profile parity of brand drug with generics