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Study aim
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In-vivo Bioequivalence Study of Palbociclib 125 mg Hard Capsules of The Test Drug (PADENZA®, Abidi Pharma, Iran) in Compared with The Reference Drug (IBRANCE® 125 mg, Pfizer Inc. Ireland) In Iranian 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 fed, and on two series of healthy volunteers. The study will be done in two periods (72h). The interval between these two periods is 2 weeks. 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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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 Palbociclib
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Intervention groups
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Intervention group 1: (IBRANCE® 125 mg, Pfizer Inc. Ireland as a reference
Intervention group 2: Palbociclib 125 mg Hard Capsules (PADENZA®, Abidi Pharma, Iran) as a test
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Main outcome variables
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Maximum drug concentration, Time to reach maximum drug concentration