Study Evaluating Serum Collected From Healthy Adults For Development of Pneumococcal Opsonophagocytic Assay
NCT ID: NCT00508950
Last Updated: 2016-08-17
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
NA
152 participants
INTERVENTIONAL
2007-08-31
2016-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
Study Groups
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All subjects
All subjects
Large volume blood draw
Large volume blood draw
Interventions
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Large volume blood draw
Large volume blood draw
Eligibility Criteria
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Inclusion Criteria
* Must have received 23vPS pneumococcal vaccine
Exclusion Criteria
* Pregnancy
* Chronic disease which could be worsened by donating blood
* Receipt of blood, blood products or immune globulin within six months
18 Years
70 Years
ALL
Yes
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Locations
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Frontage Clinical Services Inc.
Secaucus, New Jersey, United States
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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B1851075
Identifier Type: OTHER
Identifier Source: secondary_id
6115A1-1000
Identifier Type: -
Identifier Source: org_study_id
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