[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cavernous-malformation-cerebral\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cavernous-malformation-cerebral":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100594988","early-phase-1-daratumumab-for-familial-cerebral-cavernous-malformations-a-single-arm-safety-and-efficacy-study-100594988",false,"NCT07026604","Daratumumab for Familial Cerebral Cavernous Malformations: A Single-Arm Safety and Efficacy Study","A Study on the Safety and Preliminary Efficacy of the Anti-CD38 Monoclonal Antibody Daratumumab in the Treatment of Refractory Familial Cerebral Cavernous Malformations","CCM-DS01","Inclusion Criteria:\n\n* Age ≥ 18 years;\n* Diagnosed with familial cerebral cavernous malformation (familial CCM) (diagnosis requires at least one of the following: multiple CCMs or ≥2 family members with CCM);\n* Presence of clinical symptoms or history of symptomatic events: intracerebral hemorrhage, stroke, permanent or transient neurological deficits, seizures, disability, or any other neurological symptoms associated with cavernous malformations;\n* Deemed unsuitable for surgical resection by a physician;\n* Able to provide written informed consent;\n* Participant is willing and able to attend outpatient follow-up visits.\n\nExclusion Criteria:\n\n* Stable familial CCM lesions not requiring intervention;\n* Presence of metal implants or other contraindications to MRI;\n* History of statin therapy within the past 6 months;\n* History of beta-blocker therapy within the past 6 months;\n* Laboratory abnormalities: absolute neutrophil count \\\u003C1 × 10⁹\u002FL, platelet count \\\u003C100 × 10⁹\u002FL, ALT \\>2.5× upper limit of normal (ULN), ALP \\>2.5× ULN, bilirubin \\>1.5× ULN, serum creatinine \\>2× ULN;\n* Known HIV positivity, hepatitis B virus seropositivity (excluding passive immunity from vaccination or immunoglobulin therapy), defined as HBsAg-positive and\u002For anti-HBs and anti-HBc positive, or known hepatitis C virus positivity;\n* Chronic or ongoing active infections requiring systemic treatment (e.g., chronic renal infection, chronic chest infection with bronchiectasis, tuberculosis);\n* Poorly controlled comorbidities, including chronic obstructive pulmonary disease (COPD), severe asthma, poorly controlled diabetes, renal and\u002For hepatic failure;\n* Cardiovascular diseases, including unstable angina, acute myocardial infarction (within 6 months prior to screening), congestive heart failure (NYHA Class II), arrhythmias requiring treatment (excluding premature beats or minor conduction abnormalities), deep vein thrombosis (excluding stable muscular vein thrombosis as judged by the investigator), pulmonary embolism, or other severe thromboembolic events, or history of deep vein thrombosis, pulmonary embolism, or severe thromboembolic events within 6 months prior to enrollment with a risk of recurrence as assessed by the investigator;\n* Participation in other interventional medical research or clinical trials within 4 weeks prior to screening (observational, natural history, or epidemiological studies without interventions are allowed);\n* Known allergic reactions to infused protein products;\n* Pregnancy (positive urine or serum pregnancy test in premenopausal women without documented surgical sterilization) or lactation;\n* Any condition (e.g., substance abuse, alcohol dependence) that, in the investigator's opinion, may compromise the participant's compliance with study requirements;\n* Participant or legal guardian unable to provide informed consent for the study.","ALL","18 Years",{"count":20,"type":21},10,"ESTIMATED","INTERVENTIONAL",[24],"EARLY_PHASE1","Cerebral cavernous malformation (CCM) is a common vascular abnormality of the brain, affecting 0.1%-0.5% of people. It often causes recurrent brain hemorrhages, epilepsy, and neurological impairments, with surgery being the main treatment. However, surgery carries high risks for patients with multiple lesions or lesions in critical areas, and no effective pharmacological treatment is available. CCM is linked to mutations in genes like CCM1, CCM2, CCM3, or MAP3K3, which activate the MEK5-ERK5-KLF2\u002F4 pathway, disrupting endothelial function. Immune cell infiltration, particularly plasma cells with high CD38 expression, suggests a role for humoral immunity in CCM. Depleting B cells in mouse models reduced lesions and hemorrhages, but broad B cell depletion is risky.\n\nTo find a safer treatment, researchers tested anti-CD38 monoclonal antibodies in mice, showing that targeting CD38 reduced CCM lesion formation. Given the success of CD38-targeted therapies like daratumumab in treating multiple myeloma, this study proposes evaluating daratumumab for CCM in a single-center trial with 10 adult patients to assess its safety and efficacy.",[27],"Cavernous Malformation, Cerebral",[29,30,31,32],"cavernous malformation","CD38","Daratumumab","immunotherapy","NOT_YET_RECRUITING","2025-06-10",{"date":36,"type":37},"2025-06-18","ACTUAL",{"date":39,"type":21},"2025-07-01",{"date":41,"type":21},"2026-11-01",{"name":43,"class":44},"Beijing Tiantan Hospital","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":54,"sex":17,"minAge":18,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":67,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":77,"leadSponsor":79,"locationsCount":5},"100368372","quantitative-susceptibility-biomarker-and-brain-structural-property-for-cerebral-cavernous-malformation-related-epilepsy-100368372","NCT04076449","Quantitative Susceptibility Biomarker and Brain Structural Property for Cerebral Cavernous Malformation Related Epilepsy","Quantitative Susceptibility Mapping Biomarker, Brain Structure and Connectome Associated With Cerebral Cavernous Malformation Related Epilepsy and Outcome After Surgery","CRESS","Inclusion Criteria:\n\n* (1) 18 to 70 years of age\n* (2) Diagnosed with a single cerebral cavernous malformation\n* (3) No prior treatment of the symptomatic lesion\n\nExclusion Criteria:\n\n* (1) Associated with brain lesions and\u002For tumors other than CCM\n* (2) History of previous intracranial surgery\n* (3) Prior brain irradiation\n* (4) Contraindication or unwilling or unable to undergo research MRI studies\n* (5) Pregnant or breastfeeding women\n* (6) Persons unable or unlikely to return for follow-up visits\n* (7) Dementia or other progressive neurological disease",true,"70 Years",{"count":57,"type":21},200,"OBSERVATIONAL","Cerebral cavernous malformation (CCM)-related epilepsy (CRE) impairs the quality of life in patients with CCM. Patients could not always achieve seizure freedom after surgical resection of the lesion, suggesting an inadequate treatment and evaluation of the epileptogenic zone or network. Iron deposition in cerebral cavernous malformations has been postulated to play an important role in triggering CRE. Quantitative susceptibility mapping (QSM), as an optimal in vivo imaging technique to quantify iron deposition, is employed to analyze the iron quantity in CCM patients with epilepsy and further combined with brain structural and connectome analysis, to describe the difference between CCMs with and without epilepsy. In vivo biomarkers predicting CRE risk in CCM natural history and CRE control outcome after CCM surgical resection will be further identified to improve management strategy.",[27,61,62,63,64,65,66],"Cavernous Angioma","Cavernous Hemangioma","Cavernous Hemangioma of Brain","Seizures","Seizures, Epileptic","Epilepsy",[68,66,69,70,71],"Cerebral Cavernous Malformation","Quantitative Susceptibility Mapping (QSM)","Brain Connectome","Cerebral Structure","RECRUITING","2019-09-03",{"date":75,"type":37},"2019-09-04",{"date":73,"type":37},{"date":78,"type":21},"2026-12-31",{"name":80,"class":44},"yuanli Zhao"]