Sequential Medications for Juvenile Rheumatoid Arthritis
(SMART-JIA Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests different medications to determine the best treatment plan for children and teens with juvenile rheumatoid arthritis, a condition that causes joint pain and swelling. Researchers compare three medications—Abatacept, Tocilizumab, and Tofacitinib—to a type of medicine called TNFi (Tumor Necrosis Factor inhibitor), which some patients may have already tried. The goal is to identify which medication works best and the optimal order for their use. Children and teens with moderate to high joint swelling, despite taking a TNFi for at least three months, might be suitable candidates for this study. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to potentially groundbreaking treatment advancements.
Do I need to stop my current medications for the trial?
The trial does not specify if you need to stop your current medications. However, it mentions that you should not have been treated with more than one TNFi (a type of medication) before, and certain medications like systemic glucocorticoids must be at a stable dose. It's best to discuss your current medications with the trial team.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Previous studies have shown that abatacept is well tolerated by patients with juvenile idiopathic arthritis (JIA), with no new safety issues and improved symptom control for many. Research indicates that abatacept is as safe as other treatments, such as interleukin inhibitors.
Studies on tumor necrosis factor inhibitors (TNFi), including adalimumab and etanercept, demonstrate their effectiveness and general tolerability for treating JIA. However, rare reports of serious side effects, such as lymphoma, have occurred in some cases.
Tocilizumab has demonstrated good long-term safety for children with JIA. Reports indicate it remains safe over time, with many patients experiencing significant improvements.
Studies on tofacitinib suggest it is generally safe and well tolerated by patients with JIA. No major adverse events were reported, and the safety findings align with existing knowledge about the drug.
Each of these treatments has undergone various studies for safety and is generally well tolerated in children with JIA. However, as with any medication, risks exist, so discussing these options with a healthcare provider is important.12345Why are researchers excited about this trial's treatments?
Researchers are excited about these treatments for juvenile rheumatoid arthritis because they offer diverse approaches to managing the condition. Abatacept is unique as it targets a specific part of the immune system, potentially offering relief to patients who haven't responded to other medications. Tocilizumab stands out by directly blocking the inflammatory signal IL-6, offering a novel way to reduce inflammation. Tofacitinib is an oral medication that inhibits certain enzymes involved in the inflammatory process, providing a convenient alternative to injections. Finally, having a second TNFi option, like adalimumab or etanercept, gives another chance for patients who did not respond to their first TNFi treatment. These varied mechanisms provide new hope for better tailoring treatments to individual needs.
What evidence suggests that this trial's treatments could be effective for juvenile rheumatoid arthritis?
This trial will evaluate the effectiveness of different treatments for juvenile idiopathic arthritis (JIA). Research has shown that Abatacept, one of the treatments in this trial, works well for JIA. In studies, it helped control the disease and even led to remission in some patients. Long-term use proved safe and improved patients' quality of life.
Another treatment option in this trial is Tumor Necrosis Factor inhibitors (TNFi), such as adalimumab and etanercept. Patients using TNFi experienced significant improvements in their condition.
Tocilizumab, also being tested in this trial, has been effective, with many patients seeing major improvements in their symptoms. Studies found that a large number of patients had over 70% improvement.
Tofacitinib, another treatment arm in this trial, has shown lasting effectiveness for JIA, with many patients reporting significant symptom relief. It was linked to better patient-reported outcomes and remained effective over long-term use.23678Are You a Good Fit for This Trial?
This trial is for children and teens with polyarticular juvenile idiopathic arthritis (including Still's Disease) who still have moderate or high disease activity after at least 3 months on a TNFi medication. Participants must be on no or low-dose stable steroids, and consent from parent/caregiver/patient is required.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive one of the non-TNFi medications or a second TNFi, with a second randomization to assess effectiveness of changing medication if needed
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Abatacept
- TNFi (Tumor Necrosis Factor inhibitor) medication
- Tocilizumab
- Tofacitinib
Trial Overview
The study compares three different non-TNFi medications (Abatacept, Tocilizumab, Tofacitinib) to a second TNFi in kids whose arthritis didn't improve with their first TNFi. The trial uses random assignment in two stages to find the best treatment sequence.
How Is the Trial Designed?
4
Treatment groups
Active Control
Adalimumab originator or biosimilar; etanercept originator or biosimilar depending on which TNFi the participant had failed.
The 50 mg, 87.5 mg and 125 mg SQ doses will be available for weight-based dosing. All participants randomized to abatacept in the first or second stage randomization will receive abatacept SQ weekly at a dosage based on the participant's body weight
Tocilizumab will be provided in prefilled syringes (162 mg tocilizumab/0.9 mL solution). All participants randomized to tocilizumab in the first or second stage randomization will be receiving 1 prefilled syringe (162 mg) with a dosing interval based on the body weight criteria.
Tofacitinib will be provided as oral tablets (tofacitinib citrate 5 mg) and as an oral solution (1 mg/mL). All participants randomized to tofacitinib in the first or second stage randomization will receive tofacitinib oral tablets or oral solution twice daily, approximately 12 hours apart, in the morning and evening, at a dosage based on the participant's body weight .
Find a Clinic Near You
Who Is Running the Clinical Trial?
Duke University
Lead Sponsor
Patient-Centered Outcomes Research Institute
Collaborator
Citations
Efficacy and safety of abatacept for systemic juvenile ...
Conclusions: Abatacept improved the disease activity index. In addition, abatacept was as safe as interleukin-6 (IL-6) and IL-1 inhibitors.
Safety and effectiveness of abatacept in juvenile idiopathic ...
Abatacept treatment resulted in sustained disease control, including ID and clinical remission in some patients, across pcJIA and oligoarticular JIA categories ...
Abatacept as Monotherapy and in Combination With ...
ABA monotherapy (SC and IV) was effective and well tolerated in children with pcJIA when prior MTX use was ineffective or not tolerated.
Long‐Term Safety, Efficacy, and Quality of Life in Patients With ...
Long‐term abatacept treatment for up to 7 years was associated with consistent safety, sustained efficacy, and quality‐of‐life benefits in patients with JIA.
5.
acrabstracts.org
acrabstracts.org/abstract/long-term-effectiveness-and-safety-of-abatacept-in-juvenile-idiopathic-arthritis-interim-results-from-the-abatacept-in-jia-registry-2/Interim Results from the Abatacept in JIA Registry
Conclusion: In this JIA cohort, abatacept demonstrated persistent effectiveness with low MD global disease activity, low number of active joints ...
Safety and effectiveness of abatacept in juvenile idiopathic ...
Abatacept was well tolerated in patients with JIA, with no new safety signals identified and with well-controlled disease activity.
Study Details | NCT01844518 | Pharmacokinetics, Efficacy ...
A Phase 3 Multi-center, Open-Label Study to Evaluate Pharmacokinetics, Efficacy and Safety of Abatacept Administered Subcutaneously (SC) in Children and ...
Long‐Term Safety, Efficacy, and Quality of Life in Patients With ...
Long-term abatacept treatment for up to 7 years was associated with consistent safety, sustained efficacy, and quality-of-life benefits in ...
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