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Access to biologic therapies in Canada for children with juvenile idiopathic arthritis
Claire M A Leblanc1, Bianca Lang, Alma Bencivenga
1McGill University, and Department of Pediatrics, Montreal Children's Hospital, 2300 Rue Tupper, Montreal, Quebec H3H 1P3, Canada. claire.leblanc@muhc.mcgill.ca
Insights
Access to biologic therapies for children with juvenile idiopathic arthritis (JIA) in Canada is inconsistent, with significant provincial variations in coverage and criteria. This limits optimal care and necessitates policy reform for better health outcomes.
Area of Science:
- Pediatric Rheumatology
- Health Policy
- Pharmacoeconomics
Background:
- Juvenile idiopathic arthritis (JIA) is a chronic autoimmune disease affecting children.
- Biologic therapies offer effective treatment options for JIA.
- Access to these advanced treatments varies significantly within Canada.
Purpose of the Study:
- To compare access to biologic therapies for pediatric JIA patients across Canadian provinces.
- To identify provincial regulatory differences and access criteria for these treatments.
Main Methods:
- Compilation of provincial reimbursement guidelines for JIA biologics (June-August 2010).
- Multicenter, Canada-wide survey of pediatric rheumatologists regarding access experiences.
- Analysis of discrepancies in access criteria and coverage.
Main Results:
- Substantial difficulties were found in accessing biologic treatments, except for etanercept and abatacept.
- Significant provincial discrepancies in access criteria and coverage were identified.
- Age restrictions for younger children represented a notable barrier.
Conclusions:
- Canadian children with JIA may not receive internationally recognized standard care due to limited and inconsistent provincial formulary coverage.
- Urgent public policy changes are needed to improve access to biologic therapies.
- Enhanced access is crucial for optimizing short-term and long-term health outcomes for children with JIA.
Objective:
To compare access to biologic therapies for children with juvenile idiopathic arthritis (JIA) across Canada, and to identify differences in provincial regulations and criteria for access.
Methods:
Between June and August 2010, we compiled the provincial guidelines for reimbursement of biologic drugs for children with JIA and conducted a multicenter Canada-wide survey of pediatric rheumatologists to determine their experience with accessing biologic therapies for their patients.
Results:
There were significant difficulties accessing biologic treatments other than etanercept and abatacept for children. There were large discrepancies in the access criteria and coverage of biologic agents across provinces, notably with age restrictions for younger children.
Conclusion:
Canadian children with JIA may not receive optimal internationally recognized "standard" care because pediatric coverage for biologic drugs through provincial formularies is limited and inconsistent across the country. There is urgent need for public policy to improve access to biologic therapies for these children to ensure optimal short-term and longterm health outcomes.
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