cryopyrin-associated periodic syndrome
cryopyrin-associated periodic syndrome
Explore linked clinical trials. Standard reference: MONDO:00161685 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Natural History, Pathogenesis, and Outcome of Autoinflammatory Diseases (NOMID/CAPS, DIRA, CANDLE, SAVI, NLRC4-MAS, Still'S-like Diseases, and Other Undifferentiated Autoinflammatory Diseases) | Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Hypersensitivity, Immediate, Pathologic Processes, Pathological Conditions, Signs and Symptoms, STING-associated vasculopathy with onset in infancy, Skin and Connective Tissue Diseases, chronic inducible urticaria, chronic urticaria, cold urticaria, cryopyrin-associated periodic syndrome, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, immune system disorder, skin disorder, skin vascular disease, sterile multifocal osteomyelitis with periostitis and pustulosis, urticaria | Recruiting | Not stated | 2026-09-22 | NCT02974595 | |
| Repeat PET/CT Imaging in People With CAPS and Anakinra-Induced Amyloidosis Using an Amyloid-Reactive Peptide to Measure Changes in Organ-Specific Amyloid Load | Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Hypersensitivity, Immediate, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, amyloidosis, chronic inducible urticaria, chronic urticaria, cold urticaria, cryopyrin-associated periodic syndrome, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, immune system disorder, metabolic disease, proteostasis deficiencies, skin disorder, skin vascular disease, urticaria | Recruiting | Phase 1 | 2026-05-19 | NCT06974877 | |
| Ilaris NIS in Korea | Blood Protein Disorders, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Hemic and Lymphatic Diseases, Hypergammaglobulinemia, Hypersensitivity, Immediate, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Peroxisomal Disorders, Skin and Connective Tissue Diseases, TNF receptor 1-associated periodic fever syndrome, arthritic joint disease, arthropathy, autoimmune disease, brain disorder, central nervous system disorder, chronic inducible urticaria, chronic urticaria, cold urticaria, connective tissue disorder, cryopyrin-associated periodic syndrome, hematologic disorder, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, immune system disorder, immunoproliferative disorder, inborn errors of metabolism, juvenile idiopathic arthritis, metabolic disease, mevalonate kinase deficiency, musculoskeletal system disorder, nervous system disorder, rheumatic disorder, skin disorder, skin vascular disease, urticaria | Recruiting | Not stated | 2026-05-19 | NCT06838143 | |
| Circadian Rhythm Deregulation in Patients With CAPS | Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Hypersensitivity, Immediate, Muckle-Wells syndrome, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, chronic inducible urticaria, chronic urticaria, cold urticaria, cryopyrin-associated periodic syndrome, familial cold autoinflammatory syndrome, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, immune system disorder, skin disorder, skin vascular disease, urticaria | Recruiting | Not applicable | 2026-02-27 | NCT06544018 | |
| Are Mast Cells Involved in Autoinflammatory Diseases | Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Hypersensitivity, Immediate, Mast Cell Activation Disorders, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, TNF receptor 1-associated periodic fever syndrome, chronic inducible urticaria, chronic urticaria, cold urticaria, cryopyrin-associated periodic syndrome, familial Mediterranean fever, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, immune system disorder, mast cell activation syndrome, mevalonic aciduria, skin disorder, skin vascular disease, urticaria | Not yet recruiting | Not stated | 2022-03-23 | NCT05292768 |