Rheumatoid Arthritis Clinical Trial
Official title:
Observational Study With Enbrel in Patients With Rheumatoid Arthritis
The purpose of this study is to investigate the incidence of adverse events for patients with rheumatoid arthritis treated with Enbrel under usual care settings. In addition, differences in injection site reactions based on whether health care professionals or patients administer Enbrel will be assessed and evaluated.
Status | Completed |
Enrollment | 1500 |
Est. completion date | July 2005 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Proven diagnosis of rheumatoid arthritis Exclusion Criteria: - Contraindications according to Summary of Product Characteristic (SmPC)of Enbrel® the following points will prevent or restrict participation: - Patients who suffer from hypersensitivity to the active substance Etanercept or to any of the excipients of Enbrel® - Treatment with Enbrel® should not be initiated in patients with active infections including chronic or localized infections - Patients with sepsis or risk of sepsis should not be treated |
Time Perspective: Prospective
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Wyeth is now a wholly owned subsidiary of Pfizer |
Status | Clinical Trial | Phase | |
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