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This study was stopped due to lack of evidence for clinical efficacy.
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The purpose of this study in heathy people is to investigate the safety, toleration and time course of PF-03654764 in the blood, following multiple doses given by mouth together with fexofenadine.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| PF-03654764 2.5mg plus fexofenadine 60mg | Experimental |
| |
| PF-03654764 5mg plus fexofenadine 60mg | Experimental |
| |
| placebo | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PF-03654764 2.5mg plus fexofenadine 60mg | Drug | PF-03654764 2.5mg plus fexofenadine 60mg twice daily for 7 days |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with adverse events as a measure of safety and tolerability. | 30 days |
| Measure | Description | Time Frame |
|---|---|---|
| Plasma concentrations of PF-03654764 will be measured. | 7 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 Clinical Research Unit | Singapore | 188770 | Singapore |
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| Label | URL |
|---|---|
| To obtain contact information for a study center near you, click here. | View source |
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| PF-03654764 5mg plus fexofenadine 60mg | Drug | PF-03654764 5mg plus fexofenadine 60mg twice daily for 7 days |
|
| placebo | Drug | placebo given twice daily for 7 days |
|
| ID | Term |
|---|---|
| C569673 | 3-fluoro-3-(3-fluoro-4-(pyrrolidin-1-ylmethyl)phenyl)-N-(2-methylpropyl)cyclobutanecarboxamide |
| C093230 | fexofenadine |
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