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Assial - Anti Tnf Treatment in Ankylosing Spondylitis: an Observational Cohort Study in Italy (ASSIAL)

Pfizer logo

Pfizer

Status

Completed

Conditions

Ankylosing Spondylitis

Treatments

Other: no intervention

Study type

Observational

Funder types

Industry

Identifiers

NCT01856569
B1801362

Details and patient eligibility

About

Observe in real life adherence therapy and time to switch in ankylosing spondylitis patients with predominant assial involvement with 4 anti-TNF.

Full description

retrospective and prospective 150

Enrollment

152 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

retrospective:12 months at least first anti-TNF therapy prospective: at maximum 6 months observation AS patients with axial involvement

Exclusion criteria

patients in other AS studies involved

Trial design

152 participants in 1 patient group

observational
Treatment:
Other: no intervention

Trial contacts and locations

18

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Data sourced from clinicaltrials.gov

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