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An Open-label, Randomized, Single-dose, 2-sequence, 2-period, Crossover Study to Evaluate the Safety and Pharmacokinetics of AD-227 Compared to Co-administration of AD-227A and AD-227B in Healthy Adult Volunteers Under Fasting Conditions
Primary endpoint of this study is to evaluate the pharmacokinetic characteristics of AD-227 in healthy subjects.
Age
19 - No limit years
Sex
ALL
Healthy Volunteers
Yes
Central Hospital
Seoul, South Korea
Start Date
July 12, 2025
Primary Completion Date
August 13, 2025
Completion Date
August 13, 2025
Last Updated
December 1, 2025
70
ACTUAL participants
Co-administration of AD-227A and AD-227B
DRUG
Administration of AD-227
DRUG
Lead Sponsor
Addpharma Inc.
Data Source & Attribution
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