Clinical Trials in South Korea / NCT07349589
Starting soon
Phase 1
Evaluate the Safety, Tolerability and Pharmacokinetics of DW5524 in Healthy Adult Volunteers
NCT07349589 · tracked via the Priya Life Science South Korea tracker
Condition(s) studied
Healthy Adult
Investigational drug(s) / intervention(s)
DW5524DW5524-A
DW5524: DW5524
DW5524-A: DW5524-A
Study summary
This study aimed to evaluate the safety and pharmacokinetic characteristics of DW5524 in healthy adult volunteers.
Eligibility
Inclusion Criteria:
* Healthy adult volunteers aged 19 years or older at the time of screening
* Individuals weighing 50.0 kg or more and having a body mass index (BMI) between 18.0 kg/m2 and 30.0 kg/m2 at the time of screening
Exclusion Criteria:
* Those with a current or past medical history of clinically significant liver, kidney, nervous, mental, respiratory, endocrine, blood disease, tumor, genitourinary, cardiovascular, digestive, or musculoskeletal diseases.
Primary outcome measure(s)
- AUC0-t — up to 8 hour
Pharmacodynamic DW5524 - Cmax — up to 8 hour
Pharmacodynamic DW5524
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Chungbuk National University Hospital | Cheongju-si | South Korea |
More Daewon Pharmaceutical Co., Ltd. trials in South Korea
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A Phase 1 Clinical Trial to Evaluate the Safety and Pharmacokinetics of DW4421-T1 and DW4421S-T1 in Healthy Adult Volunteers
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Other trials for the same condition
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 NCT07349589 on ClinicalTrials.gov ↗ ← All trials in South Korea