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The primary purpose of this study is to evaluate the pharmacodynamics of single oral doses of PF-05175157 in healthy volunteers
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 600 mg PF-05175157 | Experimental | Subjects will receive one dose of PF-05175157. The sequence of receiving 600 mg PF-05175157 or placebo will be randomized. |
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| Placebo | Placebo Comparator | Subjects will receive one dose of placebo. The sequence of receiving placebo or 600 mg PF-05175157 will be randomized. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PF-05175157 | Drug | One single dose of PF-05175157 will be administered as a powder-in-capsule in the fasting state in the AM. |
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| Measure | Description | Time Frame |
|---|---|---|
| Changes in carbohydrate and lipid metabolism | 24 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetics: 0.5, 1, 1.5, 2.5, 6.5, 10.5, 24 hrs after dosing, parameters: Cmax, Tmax and Area under the Curve (AUC) | 24 hours |
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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 | Baton Rouge | Louisiana | 70808 | 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 |
|---|---|
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| Placebo | Drug | One single dose of placebo will be administered as a powder-in-capsule in the fasting state in the AM. |
|
| D004700 | Endocrine System Diseases |