Actively Recruiting
Bioequivalence Study for the Safety and the Pharmacokinetics of DWJ1622, DWC202313, and DWC202314 in Healthy Volunteers Under Fasting Conditions
Led by Daewoong Pharmaceutical Co. LTD. · Updated on 2025-12-17
40
Participants Needed
1
Research Sites
29 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 fasting conditions.
CONDITIONS
Official Title
Bioequivalence Study for the Safety and the Pharmacokinetics of DWJ1622, DWC202313, and DWC202314 in Healthy Volunteers Under Fasting Conditions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Over 19 years old
- Healthy adult volunteers
You will not qualify if you...
- History of mental disorder
- Female volunteers suspected of being pregnant or lactating
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
H Plus YANGJI Hospital
Seoul, Gwanak-gu, South Korea, 08779
Actively Recruiting
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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