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Starting soon Phase 1

A Phase 1 Clinical Trial to Evaluate the Safety and Pharmacokinetics of DW4421-T1 and DW4421S-T1 in Healthy Adult Volunteers

NCT07364851 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 1
Started
2026-03-06
Last updated
2026-01-23

Condition(s) studied

Healthy Adult Volunteer

Investigational drug(s) / intervention(s)

DW4421-T1DW4421S-T1 →

DW4421-T1: DW4421-T1 or DW4421S-T1

DW4421S-T1: DW4421-T1 or DW4421S-T1

Study summary

Safety and pharmacokinetic characteristics evaluation of DW4421-T1 and DW4421S-T1

Eligibility

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

Primary outcome measure(s)

  • Cmax — up to 48 hour
  • AUC0-t — up to 48 hour

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 NCT07364851 on ClinicalTrials.gov ↗ ← All trials in South Korea