Drug Rediscovery for Rare Immune Mediated Inflammatory Diseases
NCT06285539 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2026-05-12
Summary
Research into novel therapies for rare, immune-mediated inflammatory diseases (IMIDs) is limited due to small patient populations. Patients with Behçet's disease (BD), idiopathic inflammatory myopathy (IIM, also known as myositis) and IgG4-related disease (IgG4-RD) are treated with high-dosed glucocorticoids, methotrexate, azathioprine and mycophenolate mofetil, mostly for long periods of time with attendant risks of long-term toxicity, including infections. Therefore, there is an urgent need for new, more specific anti-inflammatory therapies such as targeted synthetic and biological disease-modifying antirheumatic drugs. Due to the role of type 1 interferon in both BD, IIM and IgG4-RD, JAK-STAT inhibition may be a promising treatment strategy in these conditions, because JAK1 is critical for the signal transduction of pro-inflammatory cytokine receptors. Previous research showed that JAK1 inhibition reduces activation of type 1 interferon-regulated proteins and key chemokines that control tissue inflammation.
Conditions
- Behcet's Disease
- Idiopathic Inflammatory Myopathies
- IgG4-related Disease
Interventions
- DRUG
-
Filgotinib
Filgotinib
Sponsors & Collaborators
-
Alfasigma S.p.A.
collaborator INDUSTRY -
ReumaNederland
collaborator UNKNOWN -
Autoimmune Research and Collaboration Hub
collaborator UNKNOWN -
UMC Utrecht
lead OTHER
Principal Investigators
-
Jaap M van Laar, Prof. dr. · UMC Utrecht
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-03-12
- Primary Completion
- 2026-12-31
- Completion
- 2027-12-31
Countries
- Netherlands
Study Locations
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