Clinical Trials in South Korea / NCT07784608
Starting soon
Phase 1
A Clinical Trial to Evaluate the Drug-drug Interactions of Co-administered 'HUC2-744-A' and 'HUC2-744-B' in Healthy Adult Volunteers
NCT07784608 · tracked via the Priya Life Science South Korea tracker
Condition(s) studied
Drug-drug Interactions
Investigational drug(s) / intervention(s)
Atorvastatin Calcium: HUC2-744-A
Telmisartan: HUC2-744-B
Study summary
This study aims to evaluate the pharmacokinetic interactions between HUC2-744-A and HUC2-744-B following monotherapy or co-administration under multiple-dose conditions.
Eligibility
Inclusion Criteria:
* Healthy adults
* Subjects with a body weight of 50 kg or more and a BMI within the range of 18.0 to 29.9 kg/m²
Exclusion Criteria:
* History or presence of clinically significant cardiovascular, respiratory, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurological, or psychiatric disease
* Presence of acute disease symptoms within 28 days prior to the first dosing
* History of any disease that may affect drug absorption, distribution, metabolism, or excretion
* Hypersensitivity or history of clinically significant hypersensitivity to atorvastatin, telmisartan, drugs containing ingredients of the same class, or other medications (e.g., aspirin, antibiotics, dihydropyridine derivatives)
Primary outcome measure(s)
- AUCτ — Day 22
Area Under the Curve of telmisartan, atorvastatin - Cmax,ss — Day 22
Maximum concentration at steady state of telmisartan, atorvastatin
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Korea University Anam Hospital | Seoul | Seongbuk-gu |
More Huons Co., Ltd. trials in South Korea
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 NCT07784608 on ClinicalTrials.gov ↗ ← All trials in South Korea