A Study To Assess The Effect Of PF-03526299 On Lung Function Following An Allergen Challenge In Asthmatic Subjects
NCT ID: NCT00877539
Last Updated: 2010-09-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
29 participants
INTERVENTIONAL
2009-06-30
2010-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
DOUBLE
Study Groups
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PF-03526299
PF-03526299
Inhaled, two doses 4 hours apart
Placebo
Placebo
Inhaled, two doses 4 hours apart
Fluticasone propionate
Fluticasone propionate
Inhaled
Interventions
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PF-03526299
Inhaled, two doses 4 hours apart
Placebo
Inhaled, two doses 4 hours apart
Fluticasone propionate
Inhaled
Eligibility Criteria
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Inclusion Criteria
* Mild asthma
* Atopic to allergens
Exclusion Criteria
* Smokers or recent ex-smokers
* Recent allergen challenge
18 Years
60 Years
ALL
No
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Pfizer, Inc.
Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Locations
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Pfizer Investigational Site
London, , United Kingdom
Pfizer Investigational Site
Manchester, , United Kingdom
Countries
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Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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A9291002
Identifier Type: -
Identifier Source: org_study_id