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Clinical Trial Summary

to inspect relevant pharmacokinetic parameters and relative exploitation degree, with fasting and postprandial dosing bioequivalence test under the condition of the human body, provide the basis for registration filing.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03420534
Study type Interventional
Source CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Contact
Status Active, not recruiting
Phase Phase 1
Start date November 17, 2017
Completion date March 14, 2018

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