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Clinical Trial Summary

The fed bioequivalence test adopts the experimental design of single center, single oral administration, random, open, two sequence, two cycle crossover and self-control.


Clinical Trial Description

To investigate the in vivo pharmacokinetic characteristics of ezetimibe tablets (specification 10mg) in Chinese healthy subjects after a single oral administration under fed conditions, and to evaluate the bioequivalence of ezetimibe tablets produced by Changzhou Pharmaceutical Factory Co., Ltd. and the licensee MSD Pharma (Singapore) PTE. Ltd. To study the safety of single oral ezetimibe tablets (specification 10mg) in Chinese healthy subjects. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05481385
Study type Interventional
Source The Affiliated Hospital of Qingdao University
Contact
Status Enrolling by invitation
Phase Phase 1
Start date July 15, 2022
Completion date December 30, 2022

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