Study Evaluating Enbrel in Patients With Rheumatoid Arthritis
NCT00245934 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1500
Last updated 2007-12-14
Summary
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.
Conditions
Interventions
- DRUG
-
Enbrel
Sponsors & Collaborators
-
Wyeth is now a wholly owned subsidiary of Pfizer
lead INDUSTRY
Principal Investigators
-
Medical Monitor · Wyeth is now a wholly owned subsidiary of Pfizer
-
Trial Manager · For Germany, [email protected]
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2003-06-30
- Completion
- 2005-07-31
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