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Starting soon Phase 1

Evaluate the Safety, Tolerability and Pharmacokinetics of DW5524 in Healthy Adult Volunteers

NCT07349589 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 1
Started
2026-02-01
Last updated
2026-01-20

Condition(s) studied

Healthy Adult

Investigational drug(s) / intervention(s)

DW5524DW5524-A

DW5524: DW5524

DW5524-A: DW5524-A

Study summary

This study aimed to evaluate the safety and pharmacokinetic characteristics of DW5524 in healthy adult volunteers.

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy adult volunteers aged 19 years or older at the time of screening * Individuals weighing 50.0 kg or more and having a body mass index (BMI) between 18.0 kg/m2 and 30.0 kg/m2 at the time of screening Exclusion Criteria: * Those with a current or past medical history of clinically significant liver, kidney, nervous, mental, respiratory, endocrine, blood disease, tumor, genitourinary, cardiovascular, digestive, or musculoskeletal diseases.

Primary outcome measure(s)

  • AUC0-t — up to 8 hour
    Pharmacodynamic DW5524
  • Cmax — up to 8 hour
    Pharmacodynamic DW5524

Trial sites (1)

FacilityCityRegionStatus
Chungbuk National University Hospital Cheongju-si 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 NCT07349589 on ClinicalTrials.gov ↗ ← All trials in South Korea