Juvenile Idiopathic Arthritis (JIA) Registry
- Conditions
- Juvenile Idiopathic ArthritisJIA
- Interventions
- Registration Number
- NCT00783510
- Lead Sponsor
- AbbVie
- Brief Summary
This is a global registry, to evaluate the long-term safety of Humira® in patients with moderate to severe polyarticular Juvenile Idiopathic Arthritis (JIA), that are treated as recommended in the Humira® product label. Patients treated with MTX will be considered a reference group. Patients will be followed in both the Humira® and Methotrexate (MTX) arms for 10 years from the enrollment date into one of the treatment arms.
- Detailed Description
This registry will assess the incidence and rate of Humira (monotherapy or combination therapy with MTX) or MTX observational and treatment-emergent SAEs, Adverse Events of Special Interest (AESI) and Pregnancy in patients diagnosed with moderately to severely active polyarticular or polyarticular-course JIA through Year 5. From Year 6 through Year 10 SAEs, a subset of AESI that includes congestive heart failure (CHF), malignancies, AEs at least possibly related to and/or leading to discontinuation of registry treatment and pregnancies will be collected. For JIA patients 2 to\< 4 years of age in countries with available local approval for this group of patients at the time of consent to the registry, emergent AESI, SAEs and pregnancy (at the age when a patient can become pregnant) will be collected for the full 10 years. The approved age range for HUMIRA in the U.S., European Union (EU) and in Australia is 4 years of age and older, and recent approval in EU for JIA patients 2 to \< 4 years of age.
Patients who discontinue from the registry before 10 years will be offered to participate in the direct to Health Care Provider follow-up process, as allowed by local regulations.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 849
- For a patient enrolling into the HUMIRA® arm; a pediatric patient diagnosed at any time with moderately to severely active polyarticular or polyarticular-course JIA (defined as arthritis affecting >= 5 joints at the time of diagnosis of polyarticular or polyarticular-course JIA) who has been prescribed HUMIRA® therapy according to the local approved HUMIRA® product labeling and meets one of the following criteria:
- Enrolled patients are 4 to 17 years of age as per approved HUMIRA® product label with the addition of JIA patients 2 to < 4 years of age in countries with available local approval for this group of patients at the time of consent to the registry.
- Newly initiated (within 24 months of registry entry) on HUMIRA® therapy and has received continuous (no more than 70 consecutive days off drug) HUMIRA® therapy, and the physician can provide available source documentation of SAEs, AEs of Special Interest, and dosing information since initiation of therapy;
- Or is entering after participation (within 24 months of registry entry or, if longer, continuously treated at the same site) in an AbbVie Humira sponsored study, regardless of age or the number of joints with symptoms of JIA, and has received continuous (no more than 70 consecutive days off drug) HUMIRA® therapy and the physician can provide available source documentation of SAEs, AEs of Special Interest, and dosing information since initiation of therapy.
- For a patient enrolling into the MTX arm; a pediatric patient diagnosed at any time with moderately to severely active polyarticular or polyarticular-course JIA (defined as arthritis affecting >= 5 joints at the time of diagnosis of polyarticular or polyarticular-course JIA) who is prescribed MTX therapy alone or in combination with other disease modifying anti-rheumatic drugs (DMARDs) according to the local product labeling (initiated treatment within 24 months of registry entry) and has received continuous therapy and the physician can available provide source documentation of SAEs, AEs of Special Interest, and dosing information since initiation of therapy.
- Patients who were treated in the MTX arm of this registry and prematurely discontinued from the MTX arm due to being a non-responder, or became intolerant of MTX treatment or are in need of combination treatment with HUMIRA® therapy may be eligible to enroll into the HUMIRA® treatment arm if all ongoing AEs/SAEs have been resolved, and they meet inclusion criteria and can enroll within the registry enrollment period. In case of ongoing AEs/SAEs at the time of the treatment arm switch, the AbbVie Designated Physician should be contacted to assess the eligibility of patient to roll into Humira treatment arm.
- Parent or guardian has voluntarily signed and dated an informed consent/patient authorization form, approved by an Institutional Review Board (IRB)/Independent Ethics Committee (IEC) if applicable according to local law, after the nature of the registry has been explained and the patient's parent or legal guardian has had the opportunity to ask questions. Pediatric patients will be included in all discussions as per applicable local regulations in order to obtain verbal or written assent.
- Patients should not be enrolled into the HUMIRA® or Methotrexate (MTX) arm if they cannot be prescribed and treated in accordance with the approved local HUMIRA® and/or with the local MTX product label
- Patients should not be enrolled into the HUMIRA® or MTX arm if they require on-going treatment with Kineret® (anakinra), Orencia® (abatacept), Rituxan® (rituximab), Enbrel® (etanercept), and Remicade® (infliximab), or any other approved biologic agents or investigational agents.
- Patients should not be enrolled into the MTX arm if they have had prior treatment with any investigational agent or anti-rheumatic biologic therapy such as, but not limited to, Orencia® (abatacept), Enbrel® (etanercept), Remicade® (infliximab), Rituxan® (rituximab), or Actemra® (tocilizumab)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description HUMIRA® Treatment Arm adalimumab For patients taking HUMIRA® Methotrexate Treatment Arm Methotrexate For patients taking Methotrexate
- Primary Outcome Measures
Name Time Method Incidence of Serious Adverse Events (SAEs) Up to 10 years Collected as events occur during the registry and as part of prior clinical studies. Events are collected retrospectively for patients who dosed prior to enrollment in the registry and as part of the Health Care Provider (HCP) process.
Incidence of Adverse Events (AEs) of Interest Up to 10 years Collected as events occur during the registry and as part of prior clinical studies. Events are collected retrospectively for patients who dosed prior to enrollment in the registry and as part of the Health Care Provider (HCP) process.
- Secondary Outcome Measures
Name Time Method Pediatric American College of Rheumatology (PedACR) 90 Up to 10 years Effectiveness data will be analyzed as observed and will be summarized for All Treated Patient Population.
Juvenile arthritis disease activity score (JADAS) Assessed in months 1,3, 6 and every 6 months through Year 5 Effectiveness data will be analyzed as observed and will be summarized for All Treated Patient Population. Is the total scores of four activity scales (Physician's Global Assessment of patient's disease, Parents' Global Assessment of patient's overall well-being, Number of active joints and Normalized erythrocyte sedimentation rate (ESR) if collected and available.
Physical function of the Disability Index of Childhood Health Assessment Questionnaire (DIHAQ) Assessed in months 1,3, 6 and every 6 months through Year 5 Effectiveness of therapy through clinical assessment.
Pediatric American College of Rheumatology (PedACR) 70 Up to 10 years Effectiveness data will be analyzed as observed and will be summarized for All Treated Patient Population.
Pediatric American College of Rheumatology (PedACR) - 30 Up to 10 years Effectiveness data will be analyzed as observed and will be summarized for All the Treated Patient Population.
Child Health Questionnaire (CHQ-PF50) Assessed in months 1,3, 6 and every 6 months through Year 5 The results will be summarized at each visit and will be used in exploratory analyses.
Pediatric American College of Rheumatology (PedACR) 50 Up to 10 years Effectiveness data will be analyzed as observed and will be summarized for All Treated Patient Population.
Trial Locations
- Locations (92)
AZ Arthritis and Rheumotology Research, PLLC /ID# 21023
🇺🇸Phoenix, Arizona, United States
Catalina Pointe Clinical Research /ID# 40227
🇺🇸Tucson, Arizona, United States
Arkansas Children's Hospital /ID# 23505
🇺🇸Little Rock, Arkansas, United States
Children's Hospital Los Angeles /ID# 24386
🇺🇸Los Angeles, California, United States
Children's National Medical Center /ID# 23506
🇺🇸Washington, District of Columbia, United States
Duplicate_Arthritis Associates South FL /ID# 17001
🇺🇸Delray Beach, Florida, United States
Ann & Robert H Lurie Children's Hospital of Chicago /ID# 20966
🇺🇸Chicago, Illinois, United States
The University of Chicago Medical Center /ID# 21981
🇺🇸Chicago, Illinois, United States
Methodist Medical Group Rheum /ID# 46343
🇺🇸Peoria, Illinois, United States
Indiana University /ID# 11421
🇺🇸Indianapolis, Indiana, United States
Scroll for more (82 remaining)AZ Arthritis and Rheumotology Research, PLLC /ID# 21023🇺🇸Phoenix, Arizona, United States