Browse recruiting and upcoming clinical trials for VEXAS syndrome.
Patient-friendly, AI-assisted summaries based on official ClinicalTrials.gov ↗ records. Last updated: Oct 10, 2026
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Who can join AIAdults with genetically confirmed VEXAS syndrome (UBA1 mutation), with or without myelodysplastic syndrome, requiring immunosuppressive therapy.
What is being studied AITests momelotinib treatment for VEXAS syndrome, with or without myelodysplastic syndrome.
Who can join AIPeople with VEXAS Syndome or other known or suspected autoinflammatory, autoimmune, or rheumatic diseases, their family members, and healthy volunteers.
What is being studied AICollects genetic and blood samples to study genetic causes and immune features of autoinflammatory diseases.
Who can join AIAdults older than 50 admitted to a participating Internal Medicine department with unexplained systemic inflammation or blood-cell abnormalities.
What is being studied AICollects clinical data and performs UBA1 genetic testing to identify VEXAS cases.
Who can join AIPeople diagnosed with monogenic or polygenic autoinflammatory diseases, including Behçet's disease, Still disease, PFAPA, Schnitzler, VEXAS, spondyloarthritis, Castleman disease, and non-infectious uveitis or scleritis.
What is being studied AICollects clinical, genetic, treatment, and outcome data in people with autoinflammatory diseases.
Who can join AIAdults (≥18) with inflammatory or immune-system conditions, with or without clonal hematopoiesis or related blood disorders (e.g., VEXAS, MDS/MPN, lymphoma, leukemia, MGUS).
What is being studied AICollects clinical, genetic, and outcome data on dysimmune manifestations with or without clonal hematopoiesis.