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

NCT07618845 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2026-06-01

No results posted yet for this study

Summary

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

Conditions

  • Chronic Liver Disease (CLD)

Interventions

DRUG

AD-230 (Fasted)

AD-230 1Tab., Per Oral, Fasted

DRUG

AD-230 (Fed)

AD-230 1 Tab., Per Oral, Fed state

Sponsors & Collaborators

  • Addpharma Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
19 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-05-31
Primary Completion
2026-07-31
Completion
2026-07-31

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07618845 on ClinicalTrials.gov