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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
Phase
Phase 1
Started
2026-01-27
Last updated
2026-02-11

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

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
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)

FacilityCityRegionStatus
H PLUS YANGJI HOSPITAL, Seoul Seoul South Korea Recruiting
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