Clinical Trials in South Korea / NCT07476157
Starting soon
Phase 1
A Study to Evaluate the Safety and Pharmacokinetics of AD-118 and AD-1181 in Healthy Adult Subjects
NCT07476157 · tracked via the Priya Life Science South Korea tracker
Condition(s) studied
Chronic Heart Failure
Investigational drug(s) / intervention(s)
AD-118, AD-1181: Single-dose oral administration of AD-118 or AD-1181, according to randomized sequence.
Study summary
A Study to Evaluate the Safety and Pharmacokinetics of AD-118 and AD-1181 Under Fasted Conditions in Healthy Adult Subjects
Eligibility
Inclusion Criteria:
* Body weight equal to or greater than 50kg and Body mass index (BMI) between 18.0 kg/m2 and 30.0 kg/m2 at the time of screening visit
* Subjects aged 19 years or older and under 65 years at the screening visit
Exclusion Criteria:
* Participation in another clinical study with an investigational drug within the 6 months from scheduled first administration
* Other exclusions applied
Primary outcome measure(s)
- Area under the plasma concentration-time curve during dosing interval (AUCt) — pre-dose (0hour) to 36hours
AUCt of AD-118 - Maximum concentration of drug in plasma (Cmax) — pre-dose (0hour) to 36hours
Cmax of AD-118
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| H PLUS YANGJI HOSPITAL, Seoul | Seoul | South Korea |
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Official registry record
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 NCT07476157 on ClinicalTrials.gov ↗ ← All trials in South Korea