Central Hospital
Seoul, South Korea
NCT Number: NCT06884085
Primary endpoint of this study is to evaluate the pharmacokinetic characteristics of AD-227 in healthy subjects.
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Notify Me19 year and older
All sexes
Interventional
Phase 1
Seoul, South Korea
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Co-administration of AD-227A 1Tab. and AD-227B 1Tab., Per Oral
Administration of AD-227 1Tab., Per Oral
Time frame: pre-dose (0hour) to 72hours
Cmax of AD-227
Time frame: pre-dose (0hour) to 72hours
AUCt of AD-227
Addpharma Inc.
Industry
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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