Autoimmune Research and Collaboration Hub

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Drug Rediscovery for Rare Immune Mediated Inflammatory Diseases	Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immunoglobulin G4-Related Disease, Skin and Connective Tissue Diseases, Stomatognathic Diseases, acquired idiopathic inflammatory myopathy, anterior uveitis, autoimmune disease, cardiovascular disorder, eye disorder, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, immune system disorder, mouth disorder, muscle tissue disorder, musculoskeletal system disorder, myositis disease, nervous system disorder, neuromuscular disease, panuveitis, skin disorder, skin vascular disease, uveal disorder, uveitis, vascular disorder, vasculitis	Recruiting	Phase 2	2026-05-12		NCT06285539

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