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| Name | Class |
|---|---|
| Incyte Corporation | INDUSTRY |
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This study investigates the safety, tolerability and pharmacokinetics of PF-04634817 when respectively given orally as a single tablet dose and a single dose of a solution.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| single dose PF-04634817 tablet | Active Comparator | subjects receive a single dose of PF-04634817 as a tablet |
|
| single dose PF-04634817 solution | Active Comparator | subjects receive a single dose of PF-04634817 as a solution |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PF-04634817 | Drug | single dose, 20mg, tablet |
| |
| Measure | Description | Time Frame |
|---|---|---|
| adverse events | 4 days | |
| Plasma Pharmacokinetics for both tablet and solution dosage forms. | 4 days | |
| The relative bioavailability (Frel) of PF-04634817 when administered as a tablet compared with a solution. | 4 days | |
| lab measurements | 4 days | |
| vitals/ECG parameters | 4 days |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Pfizer CT.gov Call Center | Pfizer | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pfizer Investigational Site | New Haven | Connecticut | 06511 | United States |
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| Label | URL |
|---|---|
| To obtain contact information for a study center near you, click here. | View source |
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| ID | Term |
|---|---|
| C000629947 | PF-04634817 |
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| PF-04634817 |
| Drug |
single dose, 20mg, solution |
|