Ankylosing Spondylitis Clinical Trial
Official title:
A Drug Use Investigation of Enbrel for Post-marketing Surveillance (PMS) for Ankylosing Spondylitis
To identify the following problems and questions with respect to the safety and
effectiveness of Enbrel during the post-marketing period as required by Korea Food and Drug
Administration (KFDA)'s regulations.
1. Unknown adverse reactions, especially serious adverse reactions
2. Change of the incidences of adverse reactions under the routine drug uses
3. Factors that may affect the safety of the drug
4. Factors that may affect the effectiveness of the drug
Status | Completed |
Enrollment | 526 |
Est. completion date | August 2008 |
Est. primary completion date | August 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Adults: Severe ankylosing spondylitis (AS) in patients who do not respond adequately to previous therapy Exclusion Criteria: - Patients with known hypersensitivity to Enbrel or any component of the product - Patients with sepsis or risk of sepsis - Patients with active infections including chronic or localized infections such as tuberculosis. |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Wyeth is now a wholly owned subsidiary of Pfizer |
Korea, Republic of,
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