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The purpose of this study is to evaluate the relationship between plasma drug levels and receptor binding in brain using PET; and to evaluate safety and tolerability after a single administration of PF-04995274 in healthy volunteers.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| PF-04995274 | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PF-04995274 | Drug | Single dose of up to 5 mg PF-04995274, delivered in solution on study day 1 |
|
| Measure | Description | Time Frame |
|---|---|---|
| Exposure response of overall 5HT4 receptor occupancy of PF-04995274 | up to 3 days | |
| 5HT4 receptor occupancy by PF-04995274 at regions of interest within the human brain | up to 3 days |
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events | up to 3 days | |
| change from baseline in vital signs | up to 3 days | |
| Singlet ECG post-dose |
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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 | ||
| Pfizer Investigational Site |
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| Label | URL |
|---|---|
| To obtain contact information for a study center near you, click here. | View source |
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| up to 3 days |
| Clinical safety laboratory endpoints | up to 3 days |
| Clinical examinations | up to 3 days |
| Cmax, Tmax, AUClast, and AUCinf for PF-04995274 in plasma | up to 3 days |
| Cmax, Tmax, AUClast, and AUCinf for PF-05082547 in plasma | up to 3 days |
| New Haven |
| Connecticut |
| 06519 |
| United States |
| Pfizer Investigational Site | New Haven | Connecticut | 06520 | United States |