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Starting soon Phase 1

Multiple Ascending Dose Study of DW4421

NCT07691242 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 1
Started
2026-09
Last updated
2026-07-08

Condition(s) studied

Healthy Adult Volunteers

Investigational drug(s) / intervention(s)

DW4421S-T0DW4421S-T2DW4421S-T1 →DW4421S-T3DW4421S →DW4421-3

DW4421S-T0: DW4421 5mg

DW4421S-T2: DW4421 15mg

DW4421S-T1: DW4421 20mg

DW4421S-T3: DW4421 30mg

DW4421S: DW4421 40mg

DW4421-3: Zastaprazan 20mg

Study summary

Multiple Ascending Dose of DW4421, phase I

Eligibility

Sex
ALL
Min age
19 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy adult aged 19 to 50 (inclusive) years, at the time of screening. * Subjects weighing between 50 kg and 90 kg with BMI between 18 and 27 kg/m2 (inclusive) at screening visit. Exclusion Criteria: * Those who have clinical significant liver, kidney, nervous system, respiratory, endocrine, hematology and oncology, cardiovascular, urinary, and mental diseases or past history.

Primary outcome measure(s)

  • AUCτ,ss, Area under the drug concentration-time curve of DW4421 following multiple oral administration — Day 7
    Assessment of pharmacokinetic parameters of DW4421 after multiple oral administration
  • Cmax of DW4421 following multiple oral administration — Day 7
    Assessment of pharmacokinetic parameters of DW4421 after multiple oral administration

Trial sites (1)

FacilityCityRegionStatus
Chungbuk National University Hospital Cheongju-si North Chungcheong

Other trials for the same condition

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 NCT07691242 on ClinicalTrials.gov ↗ ← All trials in South Korea