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Observational Non-Interventional Study With Enbrel (Etanercept) in Patients With Ankylosing Spondylitis

Pfizer logo

Pfizer

Status

Completed

Conditions

Spondylitis, Ankylosing

Treatments

Drug: Enbrel

Study type

Observational

Funder types

Industry

Identifiers

NCT01188655
0881X1-4456
B1801095

Details and patient eligibility

About

This observational study will be a documentation of the prescribing and administration practices of Enbrel® and their impact on ankylosing spondylitis patients outcome in a real life setting.

Full description

The study population will be described using standard descriptive statistics for demographic, clinical, medical, characteristics, as well as for standard health-related quality of life and functional disability questionnaires .

Enrollment

89 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Proven diagnosis of Ankylosing Spondylitisin accordance with local guidelines
  • Patients treated as an outpatient

Exclusion criteria

  • Patients who suffer from hypersensitivity to the active substance Etanercept or to any of the excipients of Enbrel®.
  • Treatment with Enbrel® should not be initiated in patients with active infections including chronic or localised infections.
  • Patients with sepsis or risk of sepsis should not be treated.

Trial design

89 participants in 1 patient group

Treatment Group Enbrel
Treatment:
Drug: Enbrel

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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