NCT00195364
Completed
Not Applicable
Long-Term Safety Study of Etanercept in Patients With Rheumatoid Arthritis Who Completed Trial 0881A1-301-EU in Spain
Wyeth is now a wholly owned subsidiary of Pfizer0 sites93 target enrollmentJuly 2003
DrugsEtanercept
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Rheumatoid Arthritis
- Sponsor
- Wyeth is now a wholly owned subsidiary of Pfizer
- Enrollment
- 93
- Status
- Completed
- Last Updated
- 16 years ago
Overview
Brief Summary
The purpose of this study is to evaluate long-term safety of etanercept in patients with rheumatoid arthritis who successfully have completed open-label safety study 0881A1-301-EU
Investigators
Eligibility Criteria
Inclusion Criteria
- •To have completed 0881A1-301-EU study in Spain
- •Clinical diagnosis by ACR revised criteria of rheumatoid arthritis.
Exclusion Criteria
- •Hypersensibility to etanercept or any of its components
- •Significant concurrent medical disease
Outcomes
Primary Outcomes
Not specified
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