Familial Mediterranean Fever

Browse recruiting and upcoming clinical trials for familial Mediterranean fever.

Patient-friendly, AI-assisted summaries based on official ClinicalTrials.gov ↗ records. Last updated: Oct 10, 2026

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ClinicalTrials.gov is the complete and most up-to-date source. Trials may be missing, and trial information may have changed since our last check. Always verify important information in the official registry.

34 trials + 28 related

Showing 34 trials, plus 28 related

Who can join AIAdolescents aged 13–17 with a diagnosis of Familial Mediterranean Fever (FMF).
What is being studied AITests inspiratory muscle retraining plus colchicine versus colchicine alone in adolescents with FMF
Study typeTreatment (procedure/device)
CountriesEgypt
Who can join AIPeople aged ≥6 years with colchicine‑resistant Familial Mediterranean Fever (FMF) who refuse continuous daily anakinra injections.
What is being studied AITests on-demand anakinra plus colchicine versus analgesics for pain and duration of FMF attacks.
Study typeTreatment (drug) · Phase 3
CountriesFrance
Who can join AIAdults (18–80) with familial Mediterranean fever (FMF) who completed the core RPH-104 study and received at least one dose.
What is being studied AILong-term safety and efficacy of RPH-104 (80 or 160 mg every 2 weeks) in FMF.
Study typeTreatment (drug) · Phase 2
CountriesArmenia, Russia, Turkey
Who can join AIAdults (18+) with an immune-mediated inflammatory disease such as lupus, multiple sclerosis, psoriatic arthritis, severe asthma, atopic dermatitis, angioedema, systemic sclerosis, or Behçet disease.
What is being studied AICollects clinical data, yearly disease measures, quality-of-life surveys, and blood samples for biomarker and genetic research.
Study typeOther
CountriesFrance
Who can join AIPeople with suspected or known inflammatory cardiovascular involvement from a range of conditions — for example myocarditis, pericarditis, sarcoidosis, systemic lupus erythematosus, systemic sclerosis, rheumatoid arthritis, Takayasu arteritis, and others.
What is being studied AICollects imaging and clinical data from CMR, cardiac PET, and echocardiography to detect heart involvement.
Study typeObservational
CountriesFrance
Recruiting
Who can join AIPeople with hereditary periodic fever syndromes (CAPS, crFMF, TRAPS, HIDS/MKD) or systemic juvenile idiopathic arthritis (sJIA) receiving Ilaris.
What is being studied AICollects safety and effectiveness data on Ilaris in routine clinical use.
Study typeObservational
CountriesSouth Korea
Who can join AIPeople with systemic autoimmune or autoinflammatory diseases (for example Behcet disease; ANCA-positive vasculitis; Takayasu or giant cell arteritis; Sjögren's; rheumatoid arthritis; celiac disease).
What is being studied AICollects clinical data, disease activity scores, and blood and stool samples for a biobank.
Study typeObservational
CountriesArmenia
Who can join AIPeople with NOMID/CAPS, DIRA, CANDLE, SAVI, NLRC4‑MAS, Still's or other undifferentiated autoinflammatory diseases; unaffected relatives and healthy people.
What is being studied AICollects clinical data and blood/tissue samples for genetic, immune, and biomarker studies of disease course.
Study typeObservational
CountriesUnited States
Who can join AIAdults 18–65 with Familial Mediterranean Fever and age-/sex-matched healthy volunteers.
What is being studied AITests the link between skin-measured AGEs and the CALLY inflammation index.
Study typeObservational
CountriesNot posted yet
Not yet recruiting
Who can join AIPeople with Behçet's disease and people without Behçet's disease (control participants).
What is being studied AIExamines vocal cord involvement using laryngoscopy and acoustic voice measurements.
Study typeObservational
CountriesNot posted yet
Who can join AIAdults with autoinflammatory diseases (including FMF, TRAPS, MKD, Cryopyrin Associated Periodic Syndrome, Haploinsufficiency) and matched control groups.
What is being studied AICollects clinical signs, blood/urine biomarkers, and biopsies to study mast cell involvement.
Study typeObservational
CountriesFrance
Who can join AIPeople aged 6 months–80 years with a diagnosis of Familial Mediterranean Fever (study also assesses non‑celiac gluten/wheat sensitivity).
What is being studied AICollects patient reports on whether wheat or other foods trigger FMF attacks and self-reported gluten/wheat sensitivity.
Study typeRegistry
CountriesItaly
Who can join AIPeople with monogenic or polygenic autoinflammatory diseases, for example Behçet disease, Still disease, PFAPA, Schnitzler and VEXAS.
What is being studied AICollects clinical, genetic, treatment, laboratory, radiologic and socio-economic data in a long-term registry.
Study typeRegistry
CountriesAlgeria, Australia, Belgium +19
Who can join AIAdults with rheumatic autoimmune diseases (for example rheumatoid arthritis, lupus, scleroderma, ankylosing spondylitis) and healthy adult volunteers.
What is being studied AICollects clinical data and biospecimens (blood, saliva, urine, stool, tissue) for research.
Study typeRegistry
CountriesUnited States
Who can join AIChildren and adolescents aged 10–18 with Juvenile Idiopathic Arthritis (JIA) or Familial Mediterranean Fever (FMF).
What is being studied AITests validity and reliability of two self-reported fitness questionnaires versus objective fitness tests.
Study typeRegistry
CountriesNot posted yet

Trials that may include familial Mediterranean fever (28)

ClinicalTrials.gov returned these when we searched for this condition, but we could not confirm from the registry records that they are intended for people with it. Check each trial’s eligibility criteria, and ask the study team if you are unsure.

Who can join AIPeople with multiple refractory autoimmune diseases, including Systemic Lupus Erythematosus, Systemic Sclerosis, Sjögren syndrome, and others.
What is being studied AITests BCMA‑CD19 CAR‑T cell therapy for multiple refractory autoimmune diseases.
Study typeTreatment (drug) · Phase 2
CountriesChina
Who can join AIPeople with antiphospholipid syndrome, bullous pemphigoid, Behçet's syndrome, dermatomyositis, immune‑mediated necrotizing myopathy, or immune thrombocytopenia.
What is being studied AITests multiple doses of RAY121 (classical complement pathway inhibitor) for safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy.
Study typeTreatment (drug) · Phase 1
CountriesAustralia, Austria, Bulgaria +17
Who can join AIPeople with Behçet's disease, idiopathic inflammatory myopathies (myositis), or IgG4-related disease.
What is being studied AITests daily oral filgotinib for 26 weeks on disease activity, quality of life, and safety.
Study typeTreatment (drug) · Phase 2
CountriesNetherlands
Who can join AIChildren with Behçet's disease (oral ulcers, age 2 and older) or juvenile psoriatic arthritis (age 5 to <18) who completed Week 52 of an apremilast core study.
What is being studied AITests long-term safety of apremilast in children with oral ulcers from Behçet's or JPsA.
Study typeTreatment (drug) · Phase 3
CountriesGreece, Israel, Spain +1
Who can join AIAdults aged 18–50 with Behçet's disease (diagnosed using International Study Group criteria) who had lower-extremity venous thrombosis confirmed within the past 14 days. The registry also requires either no previous vascular involvement or no previous immunosuppressive treatment for vascular involvement.
What is being studied AICompares immunosuppression alone versus immunosuppression plus rivaroxaban for Behçet-related leg clots.
Study typeTreatment (drug) · Phase 3
CountriesTurkey
Who can join AIPeople with Antiphospholipid Syndrome (APS), Bullous Pemphigoid (BP), Behçet's Syndrome (BS), Dermatomyositis (DM), Immune‑mediated Necrotizing Myopathy (IMNM), or Immune Thrombocytopenia (ITP).
What is being studied AILong-term safety, RAY121 blood levels, and complement activity.
Study typeTreatment (drug) · Phase 1
CountriesAustralia, Austria, Bulgaria +16
Who can join AIAdults with CAPS (Muckle-Wells syndrome or NOMID) who developed anakinra-induced amyloidosis and are enrolled on NIH protocol 17‑I‑0016.
What is being studied AIUses 124I-AT-01 PET/CT scans to detect and measure organ-specific amyloid in people with anakinra-induced amyloidosis.
Study typeDiagnostic
CountriesUnited States
Who can join AIPeople aged 6 years and older with genetically confirmed CAPS (familial cold urticaria, Muckle‑Wells, CINCA) and healthy household controls.
What is being studied AIMeasures circadian rhythms, melatonin timing/levels, activity, and inflammatory clock-related biomarkers in CAPS and household controls.
Study typeOther
CountriesFrance
Who can join AIPeople with mucocutaneous Behçet's syndrome.
What is being studied AICollects routine-care data to describe biosimilar ustekinumab and compare with apremilast.
Study typeObservational
CountriesFrance
Who can join AIPeople aged 1 month–99 years with PFAPA or other tonsil disorders (for example tonsillitis, obstructive sleep apnea, or sleep-disordered breathing).
What is being studied AICollects blood, tissue, and other samples to study genetics, immune features, and microbiota in tonsil disorders.
Study typeObservational
CountriesUnited States
Recruiting
Who can join AIPregnant women with vasculitis, including Behçet's disease, granulomatosis with polyangiitis, Takayasu arteritis, polyarteritis nodosa, and others.
What is being studied AICollects online questionnaires about vasculitis severity, pregnancy experiences, and pregnancy outcomes.
Study typeObservational
CountriesUnited States
Who can join AIAdults with Behçet's disease and age-matched healthy adults.
What is being studied AIMeasures serum EBI-3 protein levels by ELISA in people with Behçet's disease and controls
Study typeObservational
CountriesNot posted yet
Not yet recruiting
Who can join AIPeople with Behcet Disease and age- and sex-matched healthy volunteers.
What is being studied AIMeasures serum Asprosin and compares levels with disease activity in Behcet Disease
Study typeObservational
CountriesNot posted yet