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The study compare and evaluate the safety and pharmacokinetic characteristics between the administration of AD-116 and the administration of AD-1161 in healthy adult male volunteers
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Sequence A | Experimental | Period 1 : Reference Drug(AD-1161), Period 2 : Test Drug(AD-116) |
|
| Sequence B | Experimental | Period 1 : Test Drug(AD-116), Period 2 : Reference Drug(AD-1161) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AD-116 | Drug | AD-116 Oral Tablet |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Area under the plasma concentration-time curve during dosing interval (AUCt) | AUCt of AD-116 | pre-dose (0hour) to 72hours |
| Maximum concentration of drug in plasma (Cmax) | Cmax of AD-116 | pre-dose (0hour) to 72hours |
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Inclusion Criteria:
Exclusion Criteria:
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| ID | Term |
|---|---|
| D011470 | Prostatic Hyperplasia |
| ID | Term |
|---|---|
| D011469 | Prostatic Diseases |
| D005832 | Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
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| AD-1161 |
| Drug |
AD-1161 Oral Capsule |
|
| D052801 |
| Male Urogenital Diseases |