Last updated on December 2016

Pilot BA Study of New LY03005 vs Pristiq


Brief description of study

The objects of this study is to assess the relative bioavailability (BA) of 80 mg LY03005 oral tablets compared to 50 mg Pristiq® oral tablets after a single oral intake under fasting conditions in healthy subjects between 18 and 50 years of age.

Detailed Study Description

Twenty (20) eligible subjects will be enrolled and assigned to either LY03005 group or Pristiq group at a 1:1 ratio at one site in the USA.

Clinical Study Identifier: NCT02988024

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Clinilabs, Inc.

Eatontown, NJ United States
1.0miles
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Recruitment Status: Open


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