Juvenile Idiopathic Arthritis (JIA) Clinical Trials

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Trial of Sequential Medications AfteR TNFi Failure in Juvenile Idiopathic Arthritis

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This study is an open-label, randomized, multicenter trial that incorporates a multi-arm design comparing each of 3 non-TNFi (Tumor Necrosis Factor inhibitor) medications to a second TNFi (active control) within a sequential multiple assignment randomized trial design with 2 randomization stages corresponding with clinical decision points. The first randomization addresses whether each of the 3 non-TNFi medications is superior to treatment with a second TNFi. The second randomization allows identification of optimal sequential use of biologics (treatment strategies).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 17
Healthy Volunteers: f
View:

• Polyarticular course JIA

• Moderate or high-disease activity (cJADAS10 \>5) despite treatment with an initial TNFi for ≥3 months

• Age ≥2 years and \<18 years and weight ≥ 10kg

• No systemic glucocorticoids or systemic glucocorticoids at a stable dose of ≤0.2 mg/kg/day (maximum 10 mg/day) for ≥2 weeks prior to baseline visit

• Documented informed consent/assent obtained from the parent/caregiver/patient

Locations
United States
California
University of California San Francisco Pediatric Rheumatology
RECRUITING
San Francisco
Florida
University of Florida
RECRUITING
Gainesville
New Jersey
Hackensack Meridian Health - Joseph M. Sanzari Children's Hospital
RECRUITING
Hackensack
Ohio
Nationwide Children's Hospital
RECRUITING
Columbus
Other Locations
Germany
Asklepios Children's Hospital
RECRUITING
Sankt Augustin
Italy
IRCCS Giannina Gaslini Institute
RECRUITING
Genoa
Contact Information
Primary
Laura E Schanberg (Contact PI)
laura.schanberg@duke.edu
919-373-3863
Backup
Huiman Barnhart (Dual PI)
huiman.barnhart@duke.edu
919-668-8828
Time Frame
Start Date: 2026-01-09
Estimated Completion Date: 2026-12
Participants
Target number of participants: 400
Treatments
Active_comparator: Second TNFi (Tumor Necrosis Factor inhibitor) medication
Adalimumab originator or biosimilar; etanercept originator or biosimilar depending on which TNFi the participant had failed.
Active_comparator: Abatacept
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
Active_comparator: Tocilizumab originator or biosimilar
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.
Active_comparator: Tofacitinib
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 .
Sponsors
Leads: Duke University
Collaborators: Patient-Centered Outcomes Research Institute

This content was sourced from clinicaltrials.gov