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Special Investigation in Patients With Psoriatic Arthritis (PsA) (Working Productivity and Activity Impairment [WPAI])

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AbbVie

Status

Completed

Conditions

Psoriatic Arthritis

Study type

Observational

Funder types

Industry

Identifiers

NCT02414633
P15-084

Details and patient eligibility

About

A special investigation (post marketing observational study [PMOS]/non-mandatory) of HUMIRA® in Japanese psoriatic arthritis patients who are engaged in paid work.

Enrollment

148 patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Paid workers (including part-time) with Psoriatic Arthritis, who have never administered adalimumab, and are diagnosed by ClASsification of Psoriatic ARthritis (CASPAR) criteria

Exclusion criteria

  • Subjects showing decreased basic activities of daily life such as hospitalization and bedridden
  • Subjects with contraindications to adalimumab

Trial design

148 participants in 1 patient group

Humira
Description:
Subjects with Psoriatic Arthritis taking adalimumab under conditions of daily clinical practice.

Trial documents
1

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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