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To evaluate the safety and pharmacokinetics drug-drug interaction of YYC506-T and YYC506-A
Phase 1 to evaluate the safety and pharmacokinetics drug-drug interaction of YYC506-T and YYC506-A. Which is designed as two cohort, single-sequence, paralle, open label, multiple oral dosing.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| A Group | Experimental | Two cohort, single sequence |
|
| B Group | Experimental | Two cohort, single sequence |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| YYC506-T | Drug | single administration |
| |
| YYC506-A |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokietic parameters administration: Cmax | YYC506-T, YYC506-A, and concomitant administration Cmax | Until 48 hours |
| Pharmacokietic parameters administration: AUC | YYC506-T, YYC506-A, and concomitant administration AUC | Until 48 hours |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Min Kyu Park, PhD | ChungBuk National Unviersity Hospital. | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| ChungBuk National University Hospital | Cheongju-si | South Korea |
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| ID | Term |
|---|---|
| D050171 | Dyslipidemias |
| ID | Term |
|---|---|
| D052439 | Lipid Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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two-cohort, single-sequence, parallel, open label, multiple oral dosing study.
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| Drug |
single administration |
|
| YYC506-T + YYC506-A | Drug | concomotant administration |
|
| YYC506-A + YYC506-T | Drug | concomotant administration |
|