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Patient-Reported Efficacy of Subcutaneous (SC) Abatacept in Rheumatoid Arthritis (RA) - South Africa

Patient-Reported Efficacy of Subcutaneous Abatacept in Rheumatoid Arthritis: An Evaluation Of Patients In a Compassionate Use Programme in South Africa

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02598466
Enrollment
69
Registered
2015-11-06
Start date
2015-07-31
Completion date
2016-01-31
Last updated
2016-02-08

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

Conditions

Rheumatoid Arthritis

Brief summary

Research question: what are the patterns of patient-reported changes in physical function among adult patients using SC abatacept with moderate to severe RA since commencement of the compassionate use program (CUP).

Interventions

DRUGAbatacept

Sponsors

Hexor, South Africa
CollaboratorOTHER
Bristol-Myers Squibb
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* The global clinical trials and associated long-term extension phases imposed inclusion and

Exclusion criteria

. Only patients that completed the clinical trials and the long-term extension phase were eligible for inclusion in the CUP

Design outcomes

Primary

MeasureTime frame
Patterns of change in patient assessments of physical function with scores of the Health Assessment Questionnaire (HAQ) among users of SC Abatacept for RA since the commencement of a CUP in South Africa's private sectorApproximately 2 years

Secondary

MeasureTime frameDescription
Clinical characteristics (comorbidities including Tuberculosis, medication use, and adverse events) of patientsApproximately 2 years
Reasons for discontinuation based on the reasons mentioned in QuestionnaireApproximately 2 yearsReasons for discontinuation: defined as common responses given for stopping treatment and include death, adverse event, lack of efficacy, lost to follow-up, withdrawal of consent, or other reasons
Demographic characteristics (age, gender, education and population group) of patientsApproximately 2 years
Association of demographic and clinical characteristics based on Standard Disability Index of the Health Assessment Questionnaire (HAQ-DI) scoresApproximately 2 years
Changes in physical functioning against clinical trial and long-term extension phase data based incidence of adverse eventsApproximately 2 yearsAdverse events: defined as any untoward medical event in a patient whether related or unrelated to SC abatacept and may include any sign (laboratory finding), symptom, or disease
Reasons for skipping treatment based on the reasons mentioned in QuestionnaireApproximately 2 yearsReasons for skipping treatment: defined as explanations given for inability to adhere to the recommended treatment regime and include fear of side effects, lack of access (too far) to medicine, inconvenient to use, too busy or forgetting, or other reasons

Outcome results

None listed

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