Investigating the Utilisation and Effectiveness of Originator and Biosimilar Anti-TNF Agents

  • STATUS
    Recruiting
  • End date
    Dec 31, 2021
  • participants needed
    5000
  • sponsor
    Opal Rheumatology Ltd.
Updated on 22 January 2021
Investigator
Tegan Smith
Primary Contact
Orthopaedic and Arthritis Centre (3.5 mi away) Contact
+21 other location
tumor necrosis factor
arthritis
biosimilar
rheumatoid arthritis
spondylitis
psoriatic arthritis
ankylosing spondylitis

Summary

An observational study investigating the utilisation and effectiveness of originator and biosimilar anti-TNF agents in patients with rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis.

Details
Condition Ankylosing spondylitis, Psoriasis, PSORIATIC ARTHRITIS, Rheumatoid Arthritis, Arthritis, Arthritis and Arthritic Pain, Psoriasis and Psoriatic Disorders, Rheumatoid Arthritis (Pediatric), Arthritis and Arthritic Pain (Pediatric)
Treatment Originator, Biosimilar
Clinical Study IdentifierNCT03470688
SponsorOpal Rheumatology Ltd.
Last Modified on22 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients with a confirmed diagnosis of rheumatoid arthritis (RA), psoriatic arthritis (PsA) or ankylosing spondylitis (AS) who are being treated at a participating OPAL clinic

Exclusion Criteria

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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