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The study compare and evaluate the safety and pharmacokinetic characteristics between the administration of AD-229 and the administration of AD-2291 in healthy adults.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Sequence A | Experimental | Single-dose oral administration of AD-2291 (Rebamipide 100mg) in Period 1, followed by single-dose oral administration of AD-229 (Rebamipide 300mg) in Period 2. |
|
| Sequence B | Experimental | Single-dose oral administration of AD-229 (Rebamipide 300mg) in Period 1, followed by single-dose oral administration of AD-2291 (Rebamipide 100mg) in Period 2. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AD-229 | Drug | AD-229 Oral Tablet |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Maximum concentration of drug in plasma (Cmax) | Cmax of AD-229 | pre-dose (0hour) to 72hours |
| Area under the plasma concentration-time curve during dosing interval (AUCt) | AUCt of AD-229 | pre-dose (0hour) to 72hours |
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Inclusion Criteria:
Exclusion Criteria:
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| ID | Term |
|---|---|
| D005756 | Gastritis |
| ID | Term |
|---|---|
| D005759 | Gastroenteritis |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
| D013272 | Stomach Diseases |
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| AD-2291 |
| Drug |
AD-2291 Oral Tablet |
|