Bioequivalence Study for the Safety and the Pharmacokinetics of DWJ1622, DWC202313, and DWC202314 in Healthy Volunteers Under Fasting Conditions

Recruiting now · Phase 1

Conditions studied: Healthy Volunteers

In brief

This study aims to evaluate the safety and pharmacokinetic characteristics of DWJ1622, DWC202313, and DWC202314 in healthy adult volunteers under fasting conditions.

Key facts

Study ID

NCT07260851

Run by

Daewoong Pharmaceutical Co. LTD.

People needed

40

Starts

2025-11-05

Expected to finish

2026-05-30

Last updated by the study team

2025-12-17

Who can join

Age: 19 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Over 19 year old
• Healthy adult volunteers

You may not qualify if…

• with a history of mental disorder
• For female volunteers, those who are suspected of being pregnant or lactating

Where it is running

• H Plus YANGJI Hospital — Seoul, Gwanak-gu, South Korea (enrolling)

Full record on ClinicalTrials.gov

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