Actively Recruiting

Phase 1
Age: 19Years +
All Genders
Healthy Volunteers
NCT07267221

Bioequivalence Study for the Safety and the Pharmacokinetics of DWC202313, DWC202314, and DWJ1622 in Healthy Volunteers Under Fed Condition.

Led by Daewoong Pharmaceutical Co. LTD. · Updated on 2025-12-05

36

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Bioequivalence Study for the Safety and the Pharmacokinetics of DWC202313, DWC202314, and DWJ1622 in Healthy Volunteers Under Fed Condition.

Who Can Participate

Age: 19Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Over 19 year old
  • Healthy adult volunteers
Not Eligible

You will not qualify if you...

  • History of mental disorder
  • Female volunteers who are suspected of being pregnant or lactating

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

H Plus YANGJI Hospital

Seoul, Gwanak-gu, South Korea, 08779

Actively Recruiting

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Research Team

S

SHIN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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