hereditary periodic fever syndrome
hereditary periodic fever syndrome
Explore linked clinical trials. Standard reference: MONDO:001795367 results · Page 1 of 3
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Familial Mediterranean Fever and Related Disorders: Genetics and Disease Characteristics | Body Temperature Changes, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fever, Headache, Hypertrophy, Hypohidrosis, Neurologic Manifestations, Pain, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Skin and Connective Tissue Diseases, Splenomegaly, eye disorder, familial Mediterranean fever, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome, skin disorder, sweat gland disorder | Recruiting | Not stated | 2026-10-08 | NCT00001373 | |
| Genotype and Phenotype in Pediatric Familial Mediterranean Fever | Bacterial Infections and Mycoses, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Infections, bacterial infectious disease, brucellosis, familial Mediterranean fever, gram-negative bacterial infections, hereditary disease, hereditary periodic fever syndrome | Not yet recruiting | Not stated | 2026-10-05 | NCT07849998 | |
| Serum EBI-3 Protein Levels in Behçet's Disease | 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 | Not yet recruiting | Not stated | 2026-09-28 | NCT07845162 | |
| Corticotropin for Behçet's Disease: A Multicenter Randomized Controlled TrialAcronym. | 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 | Not yet recruiting | Phase 2 | 2026-09-22 | NCT07833163 | |
| Metabolic Syndrome Resposne to Dietary Limitations in Familial Mediterranean Fever in Adolescents | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Insulin Resistance, Nutritional and Metabolic Diseases, familial Mediterranean fever, glucose metabolism disease, hereditary disease, hereditary periodic fever syndrome, hyperinsulinism, metabolic disease | Recruiting | Not applicable | 2026-09-22 | NCT07833007 | |
| 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 | |
| Baricitinib in the Treatment of Intestinal Behçet's Syndrome | 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 | Phase 2 | 2026-09-21 | NCT06849908 | |
| Asprosin in Behect Patients | 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 | Not yet recruiting | Not stated | 2026-09-03 | NCT07803198 | |
| Inflammatory Disease Biobank for Immunophenotyping and Cardiovascular Research | Aortic Arch Syndromes, Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Spondylarthritis, Stomatognathic Diseases, Takayasu arteritis, Tako-tsubo cardiomyopathy, Ventricular Dysfunction, Ventricular Dysfunction, Left, acquired idiopathic inflammatory myopathy, anterior uveitis, anti-neutrophil cytoplasmic antibody-associated vasculitis, antiphospholipid syndrome, aortic disorder, arteritis, arthritic joint disease, arthropathy, autoimmune disease, autoimmune disorder of the nervous system, bone disorder, brain disorder, cardiomyopathy, cardiovascular disorder, central nervous system disorder, central nervous system vasculitis, cerebrovascular disorder, connective tissue disorder, eye disorder, heart disorder, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, immune system disorder, juvenile idiopathic arthritis, mouth disorder, muscle tissue disorder, musculoskeletal system disorder, myocarditis, myositis disease, necrotizing vasculitis, nervous system disorder, neuromuscular disease, panuveitis, pericarditis, rheumatic disorder, rheumatoid arthritis, skin disorder, skin vascular disease, spondylitis, spondyloarthropathy, systemic sclerosis, systemic-onset juvenile idiopathic arthritis, temporal arteritis, uveal disorder, uveitis, vascular disorder, vasculitis, vertebral column disorder | Not yet recruiting | Not stated | 2026-08-10 | NCT07737470 | |
| Apremilast Pediatric Study in Children With Active Oral Ulcers Associated With Behçet's Disease | Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Oral Ulcer, 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 | Phase 3 | 2026-07-24 | NCT04528082 | |
| Phase 1b Trial of RAY121 in Immunological Diseases (RAINBOW Trial) | Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cytopenia, Hemic and Lymphatic Diseases, Hemorrhage, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Purpura, Thrombocytopenic, Idiopathic, Signs and Symptoms, Skin Manifestations, Skin and Connective Tissue Diseases, Stomatognathic Diseases, anterior uveitis, antiphospholipid syndrome, autoimmune disease, blood coagulation disease, blood platelet disease, bullous pemphigoid, cardiovascular disorder, connective tissue disorder, dermatomyositis, eye disorder, hematologic disorder, hemorrhagic disease, 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, polymyositis, purpura, skin disorder, skin vascular disease, thrombocytopenia, thrombocytopenic purpura, thrombotic microangiopathy, uveal disorder, uveitis, vascular disorder, vasculitis, vesiculobullous skin disease | Recruiting | Phase 1 | 2026-07-22 | NCT06371417 | |
| Phase 1b Long-term Extension Trial of RAY121 in Immunological Diseases (RAINBOW-LTE Trial) | Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cytopenia, Hemic and Lymphatic Diseases, Hemorrhage, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Purpura, Thrombocytopenic, Idiopathic, Signs and Symptoms, Skin Manifestations, Skin and Connective Tissue Diseases, Stomatognathic Diseases, anterior uveitis, antiphospholipid syndrome, autoimmune disease, blood coagulation disease, blood platelet disease, bullous pemphigoid, cardiovascular disorder, connective tissue disorder, dermatomyositis, eye disorder, hematologic disorder, hemorrhagic disease, 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, polymyositis, purpura, skin disorder, skin vascular disease, thrombocytopenia, thrombocytopenic purpura, thrombotic microangiopathy, uveal disorder, uveitis, vascular disorder, vasculitis, vesiculobullous skin disease | Enrolling by invitation | Phase 1 | 2026-07-17 | NCT06723106 | |
| Diet Restiction in Subjects With Behcet Disease and Complaint of Tinnitus | Behcet disease, Body Weight, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Ear Diseases, Neurologic Manifestations, Nutritional and Metabolic Diseases, Overweight, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Skin and Connective Tissue Diseases, Stomatognathic Diseases, Tinnitus, Subjective, anterior uveitis, cardiovascular disorder, eye disorder, hearing disorder, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, mouth disorder, nervous system disorder, nutritional disorder, obesity disorder, otorhinolaryngologic disease, overnutrition, panuveitis, skin disorder, skin vascular disease, tinnitus, uveal disorder, uveitis, vascular disorder, vasculitis | Recruiting | Not applicable | 2026-07-14 | NCT07702149 | |
| Efficacy of Physical Activity Program in Metabolic-syndrome Females With Behcet Disease | Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Insulin Resistance, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, Stomatognathic Diseases, anterior uveitis, cardiovascular disorder, eye disorder, glucose metabolism disease, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, hyperinsulinism, metabolic disease, mouth disorder, panuveitis, skin disorder, skin vascular disease, uveal disorder, uveitis, vascular disorder, vasculitis | Recruiting | Not applicable | 2026-07-14 | NCT07702123 | |
| Behcet Disease Patients With Pulmonary Endoarterectomy: Outcomes of Program of Inspiratory Msucle Trianing | 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 applicable | 2026-06-23 | NCT07662603 | |
| A Study on the Use of Canakinumab Among Familial Mediterranean Fever and Still's Disease Patients | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, adult-onset Still disease, arthritic joint disease, arthropathy, autoimmune disease, connective tissue disorder, familial Mediterranean fever, hereditary disease, hereditary periodic fever syndrome, immune system disorder, juvenile idiopathic arthritis, musculoskeletal system disorder, rheumatic disorder, rheumatoid arthritis, systemic-onset juvenile idiopathic arthritis | Recruiting | Not stated | 2026-06-09 | NCT07517250 | |
| EACVI Study on Multimodality Cardiovascular Imaging of Inflammatory Cardiovascular Diseases | Aortic Arch Syndromes, Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Hypersensitivity, Delayed, Skin and Connective Tissue Diseases, Spondylarthritis, Stomatognathic Diseases, Takayasu arteritis, Tako-tsubo cardiomyopathy, Ventricular Dysfunction, Ventricular Dysfunction, Left, acquired idiopathic inflammatory myopathy, anterior uveitis, anti-neutrophil cytoplasmic antibody-associated vasculitis, aortic disorder, arteritis, arthritic joint disease, arthropathy, autoimmune disease, bone disorder, cardiomyopathy, cardiovascular disorder, connective tissue disorder, eye disorder, heart disorder, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, immune system disorder, juvenile idiopathic arthritis, lymphatic system disorder, lymphoproliferative syndrome, mouth disorder, muscle tissue disorder, musculoskeletal system disorder, myocarditis, myositis disease, necrotizing vasculitis, nervous system disorder, neuromuscular disease, panuveitis, pericarditis, rheumatic disorder, rheumatoid arthritis, sarcoidosis, skin disorder, skin vascular disease, spondylitis, systemic lupus erythematosus, systemic sclerosis, systemic-onset juvenile idiopathic arthritis, uveal disorder, uveitis, vascular disorder, vasculitis, vertebral column disorder | Recruiting | Not stated | 2026-06-05 | NCT07077304 | |
| Validity and Reliability of the International Physical Fitness Questionnaire and the Self-Perceived Health-Related Physical Fitness Questionnaire in Children and Adolescents With JIA and FMF | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, arthritic joint disease, arthropathy, autoimmune disease, connective tissue disorder, familial Mediterranean fever, hereditary disease, hereditary periodic fever syndrome, immune system disorder, juvenile idiopathic arthritis, musculoskeletal system disorder, rheumatic disorder | Not yet recruiting | Not stated | 2026-06-01 | NCT07617558 | |
| 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 | |
| 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 | |
| Deployment o the Multidisciplinary Prospective Cohort Imminent | Behcet disease, CNS demyelinating autoimmune disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypersensitivity, Immediate, Respiratory Hypersensitivity, Skin Diseases, Eczematous, Skin Diseases, Papulosquamous, Skin and Connective Tissue Diseases, Spondylarthritis, Spondylarthropathies, Stomatognathic Diseases, angioedema, anterior uveitis, arthritic joint disease, arthropathy, asthma, atopic eczema, autoimmune disease, autoimmune disorder of the nervous system, bone disorder, bronchial disorder, cardiovascular disorder, connective tissue disorder, demyelinating disease, dermatitis, eye disorder, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, immune system disorder, lung disorder, mouth disorder, multiple sclerosis, musculoskeletal system disorder, nervous system disorder, obstructive lung disease, panuveitis, psoriasis, psoriatic arthritis, respiratory system disorder, skin disorder, skin vascular disease, spondylitis, systemic sclerosis, urticaria, uveal disorder, uveitis, vascular disorder, vasculitis, vertebral column disorder | Recruiting | Not applicable | 2026-05-05 | NCT04334031 | |
| Recombinant Herpes Zoster Vaccine in Patients With Autoimmune Rheumatic Diseases | Axial Spondyloarthritis, Behcet disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Virus Infections, Dermatomyositis, Childhood Type, Herpesviridae infectious disease, Infections, Sjogren syndrome, Skin and Connective Tissue Diseases, Spondylarthritis, Spondylarthropathies, Stomatognathic Diseases, Varicella Zoster Virus Infection, Xerostomia, acquired idiopathic inflammatory myopathy, ankylosing spondylitis, ankylosis, anterior uveitis, arthritic joint disease, arthropathy, autoimmune disease, bone disorder, cardiovascular disorder, connective tissue disorder, dermatomyositis, dry eye syndrome, eye disorder, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, herpes zoster, immune system disorder, juvenile idiopathic arthritis, lacrimal apparatus disorder, mouth disorder, muscle tissue disorder, musculoskeletal system disorder, myositis disease, necrotizing vasculitis, nervous system disorder, neuromuscular disease, panuveitis, polymyositis, rheumatic disorder, rheumatoid arthritis, salivary gland disorder, skin disorder, skin vascular disease, spondylitis, spondyloarthropathy, systemic lupus erythematosus, systemic sclerosis, uveal disorder, uveitis, vascular disorder, vasculitis, vertebral column disorder, viral infectious disease | Active, not recruiting | Phase 4 | 2026-05-04 | NCT05879419 | |
| Randomized Controlled Multicenter Study Comparing Steroid Therapy Plus Anticoagulants to Steroid Therapy Alone in Deep Venous Thrombosis of Behçet's Syndrome | 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 | Phase 3 | 2026-04-23 | NCT06780462 | |
| Evaluating the Genetics and Immunology of Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Cervical Adenitis (PFAPA) Syndrome and Other Tonsil Disorders | Apnea, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyssomnias, Infections, Pharyngeal Diseases, Respiration Disorders, Skin and Connective Tissue Diseases, Sleep Disorders, Intrinsic, Stomatognathic Diseases, canker sore, hereditary disease, hereditary periodic fever syndrome, hereditary skin disorder, mouth disorder, nervous system disorder, obstructive sleep apnea syndrome, otorhinolaryngologic disease, pharyngitis, respiratory system disorder, respiratory tract infectious disorder, skin disorder, sleep apnea syndrome, sleep-wake disorder, stomatitis, tonsillitis | Recruiting | Not stated | 2026-04-08 | NCT05656365 |