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The purpose of this study is to investigate the time course of PF-00241939 concentrations in the blood following dosing by oral inhalation using dry powder inhalers.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treatment A | Experimental |
| |
| Treatment B | Experimental |
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| Treatment C | Experimental |
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| Treatment D | Active Comparator |
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| Treatment E | Active Comparator |
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| Treatment F | Active Comparator |
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| Treatment G | Active Comparator |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Treatment A | Drug | PF-00241939 300 ug using inhaler A |
| |
| Treatment B |
| Measure | Description | Time Frame |
|---|---|---|
| Plasma pharmacokinetic parameters: AUClast and Cmax. | 36 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Plasma pharmacokinetic parameters: AUC24, AUCinf, Tmax and half-life. | 36 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 | 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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| Drug |
PF-00241939 300 ug using inhaler A |
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| Treatment C | Drug | PF-00241939 300 ug using inhaler A |
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| Treatment D | Drug | PF-00241939 300 ug using inhaler B |
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| Treatment E | Drug | PF-00241939 300 ug using inhaler B |
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| Treatment F | Drug | PF-00241939 300 ug using inhaler B |
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| Treatment G | Drug | PF-00241939 300 ug using inhaler B |
|