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

An Observational Study Designed to Investigate the Utilisation and Effectiveness of Originator and Biosimilar Anti-TNF Agents in Australian Rheumatology

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03470688
Enrollment
5000
Registered
2018-03-20
Start date
2018-03-01
Completion date
2021-12-31
Last updated
2018-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rheumatoid Arthritis, Psoriatic Arthritis, Ankylosing Spondylitis

Brief 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.

Interventions

BIOLOGICALOriginator

Originator anti-TNF agents

BIOLOGICALBiosimilar

Biosimilar anti-TNF agents

Sponsors

Merck Sharp & Dohme LLC
CollaboratorINDUSTRY
Opal Rheumatology Ltd.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

\-

Design outcomes

Primary

MeasureTime frameDescription
Disease activity score based on a 28 joint count (DAS28)3 yearsComparative assessment of disease activity as measured by DAS28 in patients receiving originators vs biosimilars. Higher DAS28 scores indicate more severe disease activity.
Health Assessment Questionnaire Disability Index (HAQ-DI)3 yearsComparative assessment of disease impact on quality of life and daily physical functions in patients receiving originators vs biosimilars. HAQ-DI is designed to measure impact on everyday life. Higher scores indicate more severe disability.

Secondary

MeasureTime frameDescription
36-item Short Form Health Survey (SF-36)3 yearsComparative assessment of disease impact on quality of life in patients receiving originators vs biosimilars. The SF-36 uses 8 sub scales to assess patient vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning and mental health. Each sub scale is scored between 0-100, where lower scores indicate a greater impact on function.
Patient Health Questionnaire-2 (PHQ-2)3 yearsComparative assessment of disease impact on the emotional health in patients receiving originators vs biosimilars, as measured by the PHQ-2. The PHQ-2 is a two-question survey to screen for depression, and higher scores indicate that the patient experienced depressed mood or anhedonia more frequently over the past two weeks.
Fatigue assessed by the Functional Assessment of Chronic Illness Therapy (FACIT) questionnaire3 yearsComparative assessment of fatigue in patients receiving originators vs biosimilars, assessed using the FACIT-fatigue scale. FACIT-fatigue is a questionnaire used to measure fatigue levels in patients with rheumatoid arthritis. A higher score is associated with a greater level of fatigue.
Number of patients discontinuing the drug for safety reasons3 yearsComparison between number of patients using originator vs biosimilar who discontinue therapy for safety reasons.

Countries

Australia

Contacts

Primary ContactTegan Smith
info@opalrheumatology.com.au+61280706805

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026