Study Evaluating Enbrel (Etanercept) in Patients With Ankylosing Spondylitis
NCT00227227 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 750
Last updated 2007-12-10
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.
Conditions
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 · [email protected]
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-05-31
- Completion
- 2007-06-30
Countries
- Germany
Study Locations
More Related Trials
-
An Open-Label, Multicentre, Long-Term Extension Study of Etanercept in Ankylosing Spondylitis
NCT00421980 ·Status: COMPLETED ·Phase: PHASE3
-
Study Comparing Etanercept 50 mg Once Weekly to 25 mg Twice Weekly in Patients With Ankylosing Spondylitis
NCT00418548 ·Status: COMPLETED ·Phase: PHASE3
-
Etanercept (Enbrel) in Ankylosing Spondylitis
NCT01289743 ·Status: UNKNOWN ·Phase: PHASE2
-
Extension Study Evaluating Etanercept in Ankylosing Spondylitis
NCT00410046 ·Status: COMPLETED ·Phase: PHASE4
-
Study Evaluating Etanercept in Subjects With Ankylosing Spondylitis in Spain
NCT00873730 ·Status: COMPLETED ·Phase: PHASE4
-
An Open-Label Multicentre Long-Term Extension Study of Etanercept for Ankylosing Spondylitis
NCT00444340 ·Status: COMPLETED ·Phase: PHASE4
-
Study Evaluating Etanercept in the Treatment of Subjects With Ankylosing Spondylitis
NCT00434044 ·Status: COMPLETED ·Phase: PHASE3
-
Work Productivity in Active Ankylosing Spondylitis (AS) Patients Treated With Enbrel.
NCT01421303 ·Status: COMPLETED
-
Enbrel-Sulfasalazin-Early-Axial Spondyloarthritis (AS)
NCT00844142 ·Status: UNKNOWN ·Phase: PHASE2
-
Study Comparing Etanercept (ETN) Against a Placebo for Etanercept on a Background Nonsteroidal Anti Inflammatory Drug (NSAIDs) in the Treatment of Early Spondyloarthritis (SpA) Patients Who do Not Have X-ray Structural Changes
NCT01258738 ·Status: COMPLETED ·Phase: PHASE3
-
Study Investigating Enbrel Treatment for Ankylosing Spondylitis
NCT00195416 ·Status: COMPLETED
-
Study To Evaluate The Impact Of Early Initiation Of Biological Treatment With Ankylosing Spondylitis
NCT04507763 ·Status: COMPLETED
-
Study Evaluating the Safety of Etanercept in Rheumatoid Arthritis, Ankylosing Spondylitis and Psoriatic Arthritis
NCT00273858 ·Status: TERMINATED
-
Dose Reduction of Etanercept in Patients With Ankylosing Spondylitis
NCT02638896 ·Status: UNKNOWN ·Phase: PHASE4
-
A Study To Evaluate The Efficacy Of Enbrel (REGISTERED) Etanercept Over A Period Of 12 Months In The Routine Treatment Of Patients With Rheumatoid Arthritis, Axial Spondyloarthritis, Psoriatic Arthritis, Or Plaque Psoriasis.
NCT02486302 ·Status: COMPLETED
-
A Study of Rheumatoid Arthritis Treatment With Enbrel in Adult Patient in Outpatient Department
NCT01411215 ·Status: TERMINATED
-
Study Evaluating Etanercept and Sulphasalazine in Ankylosing Spondylitis
NCT00247962 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Evaluate the NSAIDS Sparing Effect of Etanercept in Subjects With Axial Spondyloarthritis
NCT01298531 ·Status: COMPLETED ·Phase: PHASE4
-
Study Comparing Enbrel (Etanercept) Plus Methotrexate Versus Enbrel Alone in Active Rheumatoid Arthritis Despite Current Methotrexate Therapy
NCT00244556 ·Status: COMPLETED ·Phase: PHASE4
-
Study Evaluating Enbrel in Patients With Rheumatoid Arthritis
NCT00245934 ·Status: COMPLETED
-
Etanercept (Enbrel) in Undifferentiated Spondyloarthritis
NCT01289730 ·Status: UNKNOWN ·Phase: PHASE2
-
Study Evaluating Etanercept for the Treatment of Refractory Heel Enthesitis in Spondylarthropathy
NCT00420303 ·Status: COMPLETED ·Phase: PHASE4
-
Study Evaluating the Efficacy of Enbrel (Etanercept) in Subjects in Japan
NCT00503503 ·Status: COMPLETED
-
Defining Remission With Etanercept in AS in Real Life Clinical Practice
NCT02202850 ·Status: COMPLETED
-
Study Evaluating the Safety of Enbrel (Etanercept)
NCT00683384 ·Status: COMPLETED