Bioequivalence Study for the Safety and the Pharmacokinetics of DWJ1622, DWC202313, and DWC202314 in Healthy Volunteers Under Fasting Conditions
An Open-label, Randomized, Fasting, Single-dose, 2-sequence, 2-period, Crossover Phase 1 Study to Evaluate the Pharmacokinetics and the Safety After Administration of "DWJ1622" and Co-administration of "DWC202313" and "DWC202314" in Healthy Volunteers
Daewoong Pharmaceutical Co. LTD.
40 participants
Nov 5, 2025
INTERVENTIONAL
Conditions
Summary
This study aims to evaluate the safety and pharmacokinetic characteristics of DWJ1622, DWC202313, and DWC202314 in healthy adult volunteers under fasting conditions.
Eligibility
Inclusion Criteria2
- Over 19 year old
- Healthy adult volunteers
Exclusion Criteria2
- with a history of mental disorder
- For female volunteers, those who are suspected of being pregnant or lactating
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Interventions
DWJ1622 (single oral dose) is administered in accordance with the study protocol.
DWC202313, DWC202314(single oral dose) is administered in accordance with the study protocol.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07260851