A Study to Evaluate the Safety, Pharmacokinetics of AD-118 and AD-1181 in Healthy Adult Subjects
Condition(s) studied
Investigational drug(s) / intervention(s)
AD-118, AD-1181: Single-dose oral administration of AD-118, according to randomized treatment sequence in a 2-period crossover design.
AD-118, AD-1181: Single-dose oral administration of AD-1181, according to randomized treatment sequence in a 2-period crossover design.
Study summary
A Study to Evaluate the Safety and Pharmacokinetics of AD-118 and AD-1181 Under Fasted Conditions in Healthy Adult Subjects
Eligibility
Primary outcome measure(s)
- Area under the plasma concentration-time curve during dosing interval (AUCt) — [Time Frame: pre-dose (0hour) to 36hours]
AUCt of AD-118 - Maximum concentration of drug in plasma (Cmax) — Time Frame: pre-dose (0hour) to 36hours]
Cmax of AD-118
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| H Plus Yangji Hospital | Seoul | South Korea |
More Addpharma Inc. trials in South Korea
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07717749 on ClinicalTrials.gov ↗ ← All trials in South Korea