Medical Device for Sustained Remission in Rheumatoid Arthritis Treated With Biological Therapy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorFrancisco J. Blanco

About this trial

This study aims to evaluate a new tool designed to help doctors decide whether it is safe to reduce medication in patients with rheumatoid arthritis (RA) who are in remission.

Rheumatoid arthritis is a chronic inflammatory disease that affects the joints, causing pain, stiffness, and reduced mobility. Many patients receive long-term treatment with biological drugs to control the disease. When the disease is well controlled (remission), doctors may gradually reduce the medication dose. However, deciding when and in whom to reduce treatment is currently based on experience and trial-and-error.

The study evaluates a predictive tool (called OPTIBIO) that uses information from blood samples, genetic data, and clinical characteristics to estimate the risk that the disease will flare up if treatment is reduced.

Participants in the study will be randomly assigned to one of two groups:

* In one group, the decision to reduce medication will be made by their usual doctor. * In the other group, the decision will be guided by the predictive tool.

The study lasts 12 months and includes several hospital visits. During these visits, participants will:

* Answer questionnaires about their health and quality of life * Have physical examinations * Provide blood samples for routine tests and additional research purposes * Possibly undergo joint ultrasound (if they consent) Some additional blood samples may be stored in authorized biobanks for future research related to rheumatoid arthritis, but only if participants explicitly agree. These samples will be coded to protect personal identity and will only be used in ethically approved research projects.

Participation in the study is entirely voluntary. Participants can choose which procedures they agree to and may withdraw at any time without affecting their medical care.

The study may not provide direct benefit to participants, but it could help improve future treatment decisions and the overall management of rheumatoid arthritis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults aged ≥18 years.

Diagnosis of rheumatoid arthritis according to either the 1987 American College of Rheumatology (ACR) criteria or the 2010 ACR/EULAR classification criteria.

Clinical remission for at least 6 months prior to the baseline visit, defined as DAS28-CRP < 2.6.

Receiving biological anti-TNF therapy (infliximab, adalimumab, etanercept, golimumab, or certolizumab).

Disqualifiers

Patients in whom biological therapy was prescribed due to systemic manifestations of rheumatoid arthritis.

Patients with rheumatoid arthritis and any known associated condition that may interfere with the assessment of study outcomes (e.g., fibromyalgia or concomitant chronic inflammatory diseases).

Patients receiving chronic anti-TNF biological therapy who are already undergoing treatment tapering or are on reduced or extended dosing regimens prior to study inclusion.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Predictive Model-Guided Decision Strategy

    Device

    Treatment optimization decisions are guided by the OPTIBIO predictive model, which integrates clinical variables with biomarker data derived from peripheral blood, including protein expression and genetic information. The model provides an individualized estimation of the risk of disease flare associated with treatment reduction and generates a recommendation on whether to maintain or taper biological therapy.

Treatment groups

184 Participants
are divided into 2 treatment groups
Group A: Standard of careNo intervention 0 interventions
Group B: OPTIBIO-guided decisionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Percentage of patients maintaining sustained remission.

Proportion of patients who remain in sustained remission throughout the entire follow-up period, defined as DAS28-CRP \< 2.6 based on tender joint count (28 joints), swollen joint count (28 joints), C-reactive protein levels, and patient global assessment

Time frame
Up to 12 months
2

Incidence of adverse events

Incidence and characteristics of adverse events, including serious infections requiring systemic antibiotics or hospitalization, serious treatment-related adverse events, and specific adverse reactions (e.g., infusion or injection reactions), including severity.

Time frame
Baseline to 70 days after last dose

Secondary outcomes

1

Proportion of patients achieving sustained acceptable therapeutic target

Proportion of patients maintaining an acceptable therapeutic target throughout follow-up, defined as low disease activity (DAS28-CRP \< 3.2) and absence of persistent inflammation in major joints (shoulders, elbows, hips, and knees).

Time frame
Up to 12 months
2

Proportion of patients experiencing disease flare (0-6 months).

Proportion of patients experiencing disease flare during the first 6 months of follow-up, defined as DAS28-CRP \> 2.6.

Time frame
Up to 6 months
3

Proportion of patients experiencing disease flare (6-12 months)

Proportion of patients experiencing disease flare between months 6 and 12 of follow-up, defined as DAS28-CRP \> 2.6.

Time frame
6 to 12 months
4

Number of disease flares (0-6 months)

Total number of disease flares occurring during the first 6 months of follow-up.

Time frame
Up to 6 months

Other outcomes

1

Performance of predictive models based on molecular biomarkers

Evaluation of sensitivity, specificity, and predictive values of models based on PRIME and RETRO biomarkers using clinical outcomes.

Time frame
Up to 12 months
2

Performance of predictive models based on imaging biomarkers

Evaluation of predictive performance of ultrasound-based biomarkers, including validation of deep learning models for inflammation assessment.

Time frame
Up to 12 months
3

Biobank sample collection

Collection and storage of peripheral blood samples (serum, plasma, RNA, DNA) for future biomarker research.

Time frame
Baseline

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Francisco J. Blanco

Lead sponsor

Hospital San Carlos, Madrid

Sponsor institution