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Starting soon Phase 1

A Clinical Trial to Assess the Pharmacokinetics, Safety, and Food Effect of AD-230 in Healthy Adults

NCT07618845 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 1
Started
2026-05
Last updated
2026-06-01

Condition(s) studied

Chronic Liver Disease (CLD)

Investigational drug(s) / intervention(s)

AD-230 (Fasted)AD-230 (Fed)

AD-230 (Fasted): AD-230 1Tab., Per Oral, Fasted

AD-230 (Fed): AD-230 1 Tab., Per Oral, Fed state

Study summary

A clinical trial to assess the pharmacokinetics, safety, and food effect of AD-230 in healthy adults

Eligibility

Sex
ALL
Min age
19 Years
Max age
64 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Body mass index (BMI) between 18.5 kg/m2 and 29.9 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) — -24hours to 72hours
  • Maximum concentration of drug in plasma (Cmax) — -24hours to 72hours

Trial sites (1)

FacilityCityRegionStatus
Kyungpook National university hospital Daegu South Korea
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 NCT07618845 on ClinicalTrials.gov ↗ ← All trials in South Korea