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Starting soon Phase 1

A Study to Evaluate the Safety, Pharmacokinetics of AD-118 and AD-1181 in Healthy Adult Subjects

NCT07717749 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 1
Started
2026-07-24
Last updated
2026-07-21

Condition(s) studied

Chronic Heart Failure

Investigational drug(s) / intervention(s)

AD-118, AD-1181 →AD-118, AD-1181 →

AD-118, AD-1181: Single-dose oral administration of AD-118, according to randomized treatment sequence in a 2-period crossover design.

AD-118, AD-1181: Single-dose oral administration of AD-1181, according to randomized treatment sequence in a 2-period crossover design.

Study summary

A Study to Evaluate the Safety and Pharmacokinetics of AD-118 and AD-1181 Under Fasted Conditions in Healthy Adult Subjects

Eligibility

Sex
ALL
Min age
19 Years
Max age
64 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Body weight equal to or greater than 50kg and Body mass index (BMI) between 18.0 kg/m2 and 30.0 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) — [Time Frame: pre-dose (0hour) to 36hours]
    AUCt of AD-118
  • Maximum concentration of drug in plasma (Cmax) — Time Frame: pre-dose (0hour) to 36hours]
    Cmax of AD-118

Trial sites (1)

FacilityCityRegionStatus
H Plus Yangji Hospital Seoul 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 NCT07717749 on ClinicalTrials.gov ↗ ← All trials in South Korea