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The purpose of this study is Safety, Pharmacokinetic Study of PRIC
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| A group | Experimental | Period 1: PRIC Period 2: Pranlukast hydrate |
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| B group | Experimental | Period 1: Pranlukast hydrate Period 2: PRIC |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PRIC | Drug | Pranlukast hydrate 50mg |
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| Measure | Description | Time Frame |
|---|---|---|
| Area Under the Curve (AUC) to last time point (t) | Area under the PRIC/Pranlukast dry syrup concentration in blood-time curve from zero to the final | 0, 0.5, 0.75, 1, 1.5, 1.75, 2, 2.5, 3, 4, 6, 8, 10 and 12hours postdose |
| Maximum concentration of drug (Cmax) | The maximum PRIC/Pranlukast dry syrup concentration in blood sampling time t | 0, 0.5, 0.75, 1, 1.5, 1.75, 2, 2.5, 3, 4, 6, 8, 10 and 12hours postdose |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Asan Medical Center | Seoul | Songpa-gu | South Korea |
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| Pranlukast hydrate | Drug | Pranlukast hydrate 225mg/2.25g |
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