Abatacept in Individuals Who aRe Considered At Risk of Developing Inflammatory Arthritis

NCT ID: NCT04261023

Last Updated: 2025-03-30

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-02-24
• Study Completion Date: 2021-03-15

Brief Summary

Phase II, single-centre, open label, two parallel arm cohort randomised controlled trial (RCT) testing abatacept in a population of anti-CCP Ab positive individuals at moderate to high risk of developing IA according to a published risk score, already followed in the observational study 'CCP: Next Generation'

Detailed Description

There is now evidence that the immunological disease process starts many years before the onset of clinically detectable inflammatory arthritis (IA). It is now a realistic goal to treat individuals in this pre-clinical phase with the possibility of arresting their progression to clinical disease.

Individuals at risk of developing RA can be identified by the presence of CCP antibodies alongside other clinical features. In Leeds we have developed a prediction model that stratifies these individuals into at-risk vs. low risk. At present there are no treatments in this pathway until individuals develop IA.

T-cells appear to be an appropriate target in at-risk individuals as they play a critical role in the generation and maintenance of autoimmunity. Abatacept (Orencia) is a selective T-cell modulator that blocks a co-stimulatory signal needed to activate T-cells and has an excellent safety profile.

Conditions

Inflammatory Arthritis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: SINGLE

Study Groups

Abatacept

Treatment arm - 125mg sub-cutaneous injection at week 0 and once weekly thereafter for a maximum of 48 weeks

Group Type: EXPERIMENTAL

Orencia 125 MG Per 1 ML Prefilled Syringe

Intervention Type: DRUG

Abatacept sub-cutaneous injection 125mg at week 0 and once weekly thereafter for a maximum of 48 weeks

Control arm - CCP Next Generation

Observational study cohort - usual care

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Orencia 125 MG Per 1 ML Prefilled Syringe

Abatacept sub-cutaneous injection 125mg at week 0 and once weekly thereafter for a maximum of 48 weeks

Intervention Type: DRUG

Other Intervention Names

Abatacept

Eligibility Criteria

Inclusion Criteria

• Participant in Leeds CCP 'Next Generation' observational cohort who has tested positive for anti-CCP Ab and accepted to be approached for a interventional study
• Age >18 years old.
• At moderate to high risk of progression to IA (see below).
• Consents to be contacted in future for an interventional study

A prediction model will be used to risk stratify individuals based on the following predictors:

1. Tenderness of ≥1 small joint of the hands or feet defined by the physician (one point)

2. Early morning stiffness ≥30 minutes (one point)

3. RF and/or anti-CCP Ab concentration >3x upper limit of normal. (2 points) The participant's risk will be calculated according to the model suggested by Rakieh et al. (1). Those with a score of ≥3 out of 4 will be eligible to be randomised.

• For the intervention arm:

• Randomised to intervention arm
• Consents to commence Abatacept therapy (if not, will remain in CCP Next-generation study)
• For the control arm:

• Randomised to the control arm
• Will remain in the CCP Next-generation study

Exclusion Criteria

For both the intervention and control arms:

• Previous diagnosis of RA or other form of inflammatory arthritis including, but not limited to SLE, psoriatic arthritis, ankylosing spondylitis, gout or pyrophosphate arthropathy and including current treatment with DMARDs or biological therapy
• Clinical synovitis on clinical examination by a rheumatologist
• Presence of concomitant illness likely to require systemic glucocorticosteroid therapy during the study, in the opinion of the investigator
• Treatment with an intravenous, intramuscular, intrabursal or intraarticular corticosteroid within 12 weeks prior to randomization
• Co-morbidities requiring chronic treatment with immunosuppressive or immune modulating therapy.
• Women in the intervention arm who get pregnant during the study will be withdrawn from treatment and followed for the duration of the pregnancy for safety purposes. All participants who get pregnant will continue to be followed up in clinic as standard NHS care to collect secondary end point data
• Evidence of active or latent bacterial or viral infection at the time of potential enrolment, including human immunodeficiency or herpes zoster virus or cytomegalovirus that resolved less than 2 months prior to enrolment
• Individuals with palindromic rheumatism

For the intervention arm only:

• History of acute allergic reactions to biologic therapies or immunoglobulins
• Subjects with current symptoms of severe, progressive, or uncontrolled renal, hepatic, hematologic, gastrointestinal, pulmonary, cardiac, neurologic, or cerebral disease, whether or not related to RA and which, in the opinion of the investigator, might place a subject at unacceptable risk for participation in the study
• Subjects who have at any time received treatment with any investigational drug within 28 days of the first dose of study drug
• Subjects who test positive for Hepatitis B, C or HIV.
• Subjects with tuberculosis (TB), including those at high risk of TB, chronic viral infections, recent serious bacterial infections, subjects receiving live vaccinations within 3 months of the anticipated first dose of study medication, or those with chronic illnesses that would, in the opinion of the investigator, put the participant at risk
• Subjects who currently abuse drugs or alcohol
• Subjects with a history of cancer in the last 5 years, other than non-melanoma skin cell cancers cured by local resection or carcinoma in situ
• Scheduled for or anticipating joint replacement surgery
• Men or women unwilling to use an acceptable method of contraception (detailed in 7.1.4) to avoid pregnancy for up to 14 weeks after the last dose of trial medication
• Women of childbearing potential with a positive serum or urine pregnancy test within 48 hours prior to the baseline visit. Women of child bearing potential are defined as women who have had any menstrual bleeding in the last 24 months and who have not had a hysterectomy or surgical sterilisation
• Evidence of active or latent bacterial or viral infection at the time of potential enrolment, including human immunodeficiency or herpes zoster virus or cytomegalovirus that resolved less than 2 months prior to enrolment
• Inadequate haematological, hepatic or renal function within 28 days of treatment:

• Haemoglobin <8.5 g/dL
• White blood cells <3000/mm3
• Platelets <100,000/mm3
• Serum creatinine, ALT or AST >2 times upper limit of normal
• Any other laboratory test result that, in the opinion of the study investigator, might place the participant at unacceptable risk for participation in the study

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Leeds

OTHER

Sponsor Role: lead

Responsible Party

Paul Emery

Professor of Rheumatology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Institute of Rheumatic & Musculoskeletal Medicine, Chapel Allerton Hospital

Leeds, WEST Yorkshire, United Kingdom

Countries

United Kingdom

Other Identifiers

RR15/348

Identifier Type: -

Identifier Source: org_study_id