Clinical Trials in South Korea / NCT07385235
Recruiting
Phase 1
Compare and Evaluate the Safety and PK Data of a Single Dose Administration of 'AD-115A' or 'AD-1151'
NCT07385235 · tracked via the Priya Life Science South Korea tracker
Condition(s) studied
Gastric Ulcer
Investigational drug(s) / intervention(s)
AD-115A, AD-1151
AD-115A, AD-1151: Single-dose oral administration of AD-115A or AD-1151 (200 mg tablet), according to randomized sequence.
Study summary
The study compare and evaluate the safety and pharmacokinetic characteristics of a single dose administration of 'AD-115A' or 'AD-1151' in healthy adults.
Eligibility
Inclusion Criteria:
* The Age equal to or greater than 19 in healthy volunteers at the time of screening visit
* Body mass index (BMI) between 18.0 kg/m2 and 30.0 kg/m2 at the time of screening visit
Exclusion Criteria:
* Individuals who have taken drugs that induce (e.g., barbiturates) or inhibit drug-metabolizing enzymes within 30 days prior to the start of the study (first dosing day), or have taken drugs that may affect this study within 10 days prior to the start of the study (first dosing day)
* Other exclusions applied
Primary outcome measure(s)
- Maximum concentration of drug in plasma (Cmax) — pre-dose to 24 hours
Cmax of AD-115A - Area under the plasma concentration-time curve during dosing interval (AUCt) — pre-dose to 24 hours
AUCt of AD-115A
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| H PLUS YANGJI HOSPITAL, Seoul | Seoul | South Korea | Recruiting |
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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 NCT07385235 on ClinicalTrials.gov ↗ ← All trials in South Korea