Service de médecine interne-APHP - Henri Mondor

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Ustekinumab in BEhçet's Syndrome STudy	Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Stomatognathic Diseases, anterior uveitis, cardiovascular disorder, eye disorder, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, mouth disorder, panuveitis, skin disorder, skin vascular disease, uveal disorder, uveitis, vascular disorder, vasculitis	Recruiting	Not stated	2025-11-24		NCT07244614

Clinical trials