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To evaluate the pharmacokinetic interactions of AD-231A, AD-231B, and AD-231C in healthy adult volunteers.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm A | Experimental | Period 1 : Treatment A(AD-231A), Period 2 : Treatment C(AD-231A+AD-231B+AD-231C) |
|
| Arm B | Experimental | Period 1 : Treatment B(AD-231B+AD-231C), Period 2 : Treatment C(AD-231A+AD-231B+AD-231C) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Treatment A(AD-231A) | Drug | AD-231A Oral Tablet |
| |
| Treatment B(AD-231B+AD-231C) |
| Measure | Description | Time Frame |
|---|---|---|
| Area under the plasma concentration-time curve during dosing interval at steady state (AUCÏ„,ss) | AUCÏ„,ss | pre-dose (0hour) to 24 hours post-dose on Day 14 |
| Maximum concentration of drug in plasma at steady state (Cmax,ss) | pre-dose (0hour) to 24 hours post-dose on Day 14 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| JaeHun Jung | Contact | +8247679615 | jhjung@addpharma.co.kr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| H+ Yangji Hospital | Seoul | South Korea |
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| ID | Term |
|---|---|
| D006973 | Hypertension |
| D006949 | Hyperlipidemias |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D050171 | Dyslipidemias |
| D052439 | Lipid Metabolism Disorders |
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| Drug |
AD-231B+AD-231C Oral Tablet |
|
| Treatment C(AD-231A+AD-231B+AD-231C) | Drug | AD-231A+AD-231B+AD-231C Oral Tablet |
|
| D008659 |
| Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |