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

  • STATUS
    Recruiting
  • participants needed
    5000
  • sponsor
    Opal Rheumatology Ltd.
Updated on 8 November 2020
Orthopaedic and Arthritis Centre (3.5 mi away) Contact
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
Treatment Originator, Biosimilar
Clinical Study IdentifierNCT03470688
SponsorOpal Rheumatology Ltd.
Last Modified on8 November 2020

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Eligibility

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Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: Ankylosing spondylitis or Rheumatoid Arthritis or PSORIATIC ARTHRITIS?
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
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Step 2 Get screened

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

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Step 3 Enroll in the clinical study

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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Step 4 Get your study results

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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