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Clinical Trial Summary

The objective of this study is to evaluate relative bioavailability between 80 mg LY03005 oral tablets and 50 mg Pristiq® oral tablets after a single dose of each drug in a cross-over 2-period design under fasting condition in healthy subjects between 18 and 50 years of age.


Clinical Trial Description

Twenty (20) eligible subjects will be enrolled and assigned to either Group A or Group B at a 1:1 ratio. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03357796
Study type Interventional
Source Luye Pharma Group Ltd.
Contact
Status Completed
Phase Phase 1
Start date November 27, 2017
Completion date December 22, 2017

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