A Randomized, Double Blind, Placebo Controlled Phase 2 Study To Assess The Immune Response Following Administration Of Influenza And Pneumococcal Vaccines To Subjects With Rheumatoid Arthritis Receiving Cp-690,550 Or Placebo Cp-690,550 With And Without Ba
| City: |
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Clarksburg |
| State: |
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West Virginia |
| Zip Code: |
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26301 |
| Conditions: |
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Rheumatoid Arthritis |
| Purpose: |
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A Randomized, Double Blind, Placebo Controlled Phase 2 Study To assess the Immune Response
Following Administration of Influenza and Pneumococcal Vaccines to Subjects with Rheumatoid
Arthritis receiving CP-690,550 with and Without background Methotrexate
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| Study Summary: |
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| Criteria: |
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Inclusion Criteria:
- The subject must meet the American College of Rheumatology (ACR) classification
criteria for the diagnosis of RA by satisfying at least four of the seven criteria.
- The subject must have active disease at both screening and baseline
Exclusion Criteria:
- History of any documented influenza or pneumococcal infection within the last 3
months.
- Receipt of any vaccine within 1 month prior to the initial study drug administration
(CP-690,550 or placebo CP-690,550).
- If a subject has received an influenza vaccine within 6 months or a pneumococcal
vaccine within 5 years of initial study drug administration.
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| NCT ID: |
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NCT01359150 |
| Primary Contact: |
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Study Director Pfizer CT.gov Call Center Pfizer
Pfizer CT.gov Call Center Phone: 1-800-718-1021
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| Backup Contact: |
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N/A |
| Location Contact: |
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Clarksburg, West Virginia 26301 United States
There is no listed contact information for this specific location.
Site Status: Completed |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 18, 2013 |
| Modifications to this listing: |
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