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Clinical Trial Summary

Primary endpoint of this study is to evaluate the pharmacokinetic characteristics of AD-221 in healthy male subjects.

Clinical Trial Description

The purpose of this study is to evaluate the pharmacokinetic characteristics and safety profiles of AD-221 compared with coadministration AD-221A and AD-221B in healthy male subjects. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05202405
Study type Interventional
Source Addpharma Inc.
Status Completed
Phase Phase 1
Start date January 5, 2022
Completion date March 4, 2022

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