Clinical Trials in South Korea / NCT07618845
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
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Kyungpook National university hospital | Daegu | 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 NCT07618845 on ClinicalTrials.gov ↗ ← All trials in South Korea