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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00227227
Other study ID # 101540
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated December 7, 2007
Start date May 2004
Est. completion date June 2007

Study information

Verified date December 2007
Source Wyeth is now a wholly owned subsidiary of Pfizer
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate the incidence of adverse events for patients with AS treated with Enbrel in usual care settings.


Recruitment information / eligibility

Status Completed
Enrollment 750
Est. completion date June 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Diagnosis of ankylosing spondylitis

Exclusion Criteria:

- Contraindications according SmPC

Study Design

Time Perspective: Prospective


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Wyeth is now a wholly owned subsidiary of Pfizer

Country where clinical trial is conducted

Germany, 

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