[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"fronto-temporal-dementia\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:fronto-temporal-dementia":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,50],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100562542","phase-2-vortioxetine-for-the-treatment-of-mood-and-cognitive-symptoms-in-frontotemporal-dementia-100562542",false,"NCT06604520","Vortioxetine for the Treatment of Mood and Cognitive Symptoms in Frontotemporal Dementia","Functional Neuroimaging to Examine Affective Symptoms and Cognition in Frontotemporal Dementia","FTD Patients\n\nInclusion Criteria:\n\n1. Male or Female\n2. Age 45 and above\n3. Diagnosis of possible or probable bvFTD based on international consensus criteria for behavioral variant FTD (FTDC)\n4. The presence of at least one of the following affective symptoms on the 12-item Neuropsychiatric Inventory: depression, anxiety, irritability, or agitation\n5. A global Clinical Dementia Rating (CDR®) plus National Alzheimer's Coordinating Center (NACC) Frontotemporal lobar degeneration (FTLD) Behavior and Language Domains global score (CDR® plus NACC FTLD) less than or equal to one\n6. Patients must be medically stable\n7. Vortioxetine treatment is clinically indicated\n8. Competent to provide informed consent\n\nExclusion Criteria:\n\n1. No history of drug or alcohol dependence within six months prior to study entry\n2. Negative toxicology screening for drugs of abuse\n3. Subject must not be pregnant or nursing\n4. No contraindications to Vortioxetine treatment\n5. No contraindications for Magnetic Resonance (MR) scanning (e.g. metal implanted in the body)\n\nHealthy Controls\n\nInclusion Criteria:\n\n1. Male or Female\n2. Age 45 and above\n3. Subjects must be medically stable\n4. Free of psychotropic medications\n5. Competent to provide informed consent\n\nExclusion Criteria:\n\n1. No current or past history of neurological or psychiatric illness or substance abuse\n2. Subject must not be pregnant or nursing\n3. Negative toxicology screening for drugs of abuse\n4. No contraindications for MR scanning (e.g. metal implanted in the body)",true,"ALL","45 Years",{"count":20,"type":21},50,"ESTIMATED","INTERVENTIONAL",[24],"PHASE2","The goal of this clinical trial is to learn if vortioxetine improves mood symptoms and cognition in patients with early-stage behavioral variant Frontotemporal Dementia (bvFTD). The main questions this study aims to answer are:\n\n1. Do individuals with mood symptoms and bvFTD have brain changes and cognitive profiles that differ compared to individuals without bvFTD?\n2. Do mood symptoms and cognition improve following treatment with vortioxetine?\n\nResearchers will also determine whether there are changes in the brain associated with vortioxetine treatment.\n\nParticipants will:\n\n* Undergo a screening visit that involves clinical assessments and laboratory tests\n* Undergo an initial brain magnetic resonance imaging (MRI) and fluorodeoxyglucose (18F) Positron Emission Tomography (FDG PET) scan before starting treatment with vortioxetine\n* Undergo memory and problem-solving tests before starting treatment with vortioxetine\n* Undergo approximately 12 weeks of treatment with vortioxetine, during which time there will be regular contact and assessments with the study psychiatrist\n* Undergo a repeat PET scan and repeat memory and problem-solving tests after 12 weeks of treatment with vortioxetine",[27,28,29,30,31,32],"Fronto-temporal Dementia","Fronto-temporal Lobar Dementia","Frontotemporal Degeneration","Frontotemporal Dementia (FTD)","Frontotemporal Dementia, Behavioral Variant","Frontotemporal Dementia",[34,32,35,36],"FTD","Neuropsychiatric Symptoms","Antidepressant","RECRUITING","2026-03-05",{"date":40,"type":41},"2026-03-09","ACTUAL",{"date":43,"type":41},"2025-03-20",{"date":45,"type":21},"2029-09-01",{"name":47,"class":48},"Johns Hopkins University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":61,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":75,"leadSponsor":77,"locationsCount":49},"100562802","phase-1-huc-msc-sev-001-nasal-drops-for-neurodegenerative-diseases-100562802","NCT06607900","hUC-MSC-sEV-001 Nasal Drops for Neurodegenerative Diseases","A Multi-center, Open, Single-arm, Basket-design Clinical Trial to Evaluate the Safety and Efficacy of Human Umbilical Cord Mesenchymal Stem Cell-derived Small Extracellular Vesicles hUC-MSC-sEV-001 Nasal Drops for the Treatment of Multiple Neurodegenerative Diseases","General Criteria:\n\nInclusion Criteria:\n\n1. Age 18-80 years (inclusive), any gender.\n2. Subjects or their legal guardians voluntarily sign a written informed consent form and are able to comply with the study requirements for dosing and follow-up.\n\nExclusion Criteria:\n\n1. Subjects who have received allogeneic mesenchymal progenitor cell therapy or its derived small extracellular vesicles.\n2. Subjects with abnormal nasal anatomy, nasal damage, severe rhinitis, or other nasal conditions that may affect the administration of the investigational product.\n3. Subjects requiring nasogastric tube insertion.\n4. Suffering from other uncontrolled diseases that may interfere with the study results, including but not limited to severe local infection, systemic infection, or immunodeficiency.\n5. Combined with malignant tumors, hematological malignancies, or other serious systemic diseases.\n6. Clinically significant history of allergic reactions, especially drug allergic reactions.\n7. Severe renal insufficiency: creatinine clearance (CrCl) \\\u003C 30 mL\u002Fmin (calculated by Cockcroft-Gault formula), or other known severe renal diseases.\n8. Peripheral blood hemoglobin (HGB) \\\u003C 100 g\u002FL, absolute neutrophil count (NEUT) \\\u003C 1.5 × 10⁹\u002FL, platelet count (PLT) \\\u003C 100 × 10⁹\u002FL, white blood cell count (WBC) \\\u003C 4.0 × 10⁹\u002FL or ≥ 12 × 10⁹\u002FL, serum albumin \\\u003C 30 g\u002FL; alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≥ 3 × upper limit of normal (ULN).\n9. HBsAg positive, or HBcAb positive with HBV DNA positive, hepatitis C virus (HCV) antibody positive, peripheral blood HCV RNA positive, HIV antibody positive; CMV DNA positive, syphilis serology positive.\n10. Contraindications to MRI examination (e.g., metal implants) or inability to tolerate MRI (e.g., claustrophobia).\n11. Women of childbearing potential not intending to use effective contraception during the trial or within 90 days after the last dose and with a positive pregnancy test record; pregnant or lactating women; men who are sexually active during the trial or within 90 days after the last dose and not intending to use effective contraception; or men planning to donate sperm during the trial or within 90 days after the last dose.\n12. Vaccination within 1 month prior to the first dose or planned during the period from enrollment until the end of follow-up.\n13. Participation in other clinical drug studies within the past 30 days.\n14. Any condition that, in the investigator's judgment, may compromise the subject's ability to understand and\u002For comply with the study procedures and\u002For follow-up.\n\nAlzheimer's Disease (AD) Specific Criteria:\n\nInclusion Criteria:\n\n1. Probable AD as defined by the 2011 National Institute on Aging-Alzheimer's Association (NIA-AA) criteria.\n2. Clinical Dementia Rating (CDR) score ≤ 1.0.\n3. Subjects have an identified, reliable caregiver.\n4. Stable treatment regimen for at least 1 month prior to dosing.\n\nExclusion Criteria:\n\n1. Major history of significant brain injury with persistent neurological impairment (with or without) or known structural brain abnormalities.\n2. Cognitive impairment due to other causes: central nervous system infection, Creutzfeldt-Jakob disease, traumatic dementia, other physical\u002Fchemical factors (e.g., drug intoxication, alcoholism, carbon monoxide poisoning), major systemic illnesses (e.g., hepatic encephalopathy, pulmonary encephalopathy), intracranial space-occupying lesions (e.g., subdural hematoma, brain tumor), endocrine disorders (e.g., thyroid disease, parathyroid disease), vitamin B12 or folate deficiency, or any other known causes.\n\nParkinson's Disease (PD) Specific Criteria:\n\nInclusion Criteria:\n\n1. Diagnosis of PD according to the 2015 Movement Disorder Society (MDS) clinical diagnostic criteria for PD.\n2. Hoehn and Yahr stage ≤ 3.\n3. Stable treatment regimen for at least 1 month prior to dosing.\n\nExclusion Criteria:\n\n1\\. Parkinsonism other than PD, including but not limited to progressive supranuclear palsy (PSP), multiple system atrophy (MSA), vascular parkinsonism, drug-induced parkinsonism, essential tremor, primary dystonia.\n\nMultiple System Atrophy (MSA) Specific Criteria:\n\nInclusion Criteria:\n\n1. Diagnosis of possible or probable multiple system atrophy.\n2. Time since diagnosis \\\u003C 3 years from baseline, with an expected survival of at least 3 years.\n3. Stable treatment regimen for at least 1 month prior to dosing.\n\nExclusion Criteria:\n\n1. Modified Unified Multiple System Atrophy Rating Scale (UMSARS) Part I score ≥ 14.\n2. Presence of any condition that, in the investigators' judgment, affects the diagnosis or assessment of MSA.\n\nDementia with Lewy Bodies (DLB) Specific Criteria:\n\nInclusion Criteria:\n\n1. Meets the revised consensus criteria for DLB (Fourth Consensus Report of the DLB Consortium, 2017).\n2. Severity of motor symptoms must be ≤ stage 3 on the Hoehn and Yahr scale.\n3. Clinical Dementia Rating (CDR) score ≤ 1.0.\n4. Stable treatment regimen for at least 1 month prior to dosing.\n\nExclusion Criteria:\n\n1. Patients currently diagnosed with any primary psychiatric disorder (e.g., schizophrenia, bipolar disorder, or major depressive episode) according to DSM-V.\n2. Patients with clinically significant or unstable systemic illness and exposure to toxicants within the past 5 years.\n\nFrontotemporal Dementia (FTD) Specific Criteria:\n\nInclusion Criteria:\n\n1. Meets the 2017 International Research Society (IRS) diagnostic criteria for FTD.\n2. Clinical Dementia Rating (CDR) score ≤ 1.0.\n3. Stable treatment regimen for at least 1 month prior to dosing.\n\nExclusion Criteria:\n\n1\\. Diagnosis of severe central nervous system diseases other than FTD that may be the cause of the patient's FTD symptoms or may affect the study objectives.\n\nAmyotrophic Lateral Sclerosis (ALS) Specific Criteria:\n\nInclusion Criteria:\n\n1. Diagnosis of Amyotrophic Lateral Sclerosis (ALS) meeting the diagnostic criteria (Revised El Escorial Criteria, 2000 or Airlie House Criteria) at the level of definite, probable, or laboratory-supported probable ALS.\n2. Disease duration ≥ 6 months and ≤ 2 years (from the first occurrence of any ALS symptom).\n3. Revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R) score: each individual item score ≥ 2 points (with the three respiratory items - Dyspnea, Orthopnea, and Respiratory Insufficiency - all scoring 4 points).\n4. Stable treatment regimen for at least 1 month prior to dosing.\n\nExclusion Criteria:\n\n1\\. Diagnosis of non-ALS patients based on clinical presentation and available auxiliary clinical examinations (neurophysiology, MRI or other imaging techniques, laboratory tests, etc.).","18 Years","80 Years",{"count":60,"type":21},120,[62],"PHASE1","To evaluate the safety and preliminary efficacy of human umbilical cord mesenchymal stem cell-derived small extracellular vesicles hUC-MSC-sEV-001 nasal drops in multiple neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, multiple system atrophy, Lewy body dementia, frontotemporal dementia, and amyotrophic lateral sclerosis.",[65,66,67,68,27,69],"Alzheimer Disease","Parkinson Disease","Lewy Body Dementia","Multiple System Atrophy","Amyotrophic Lateral Sclerosis","NOT_YET_RECRUITING","2025-07-01",{"date":73,"type":41},"2025-07-08",{"date":71,"type":21},{"date":76,"type":21},"2028-08-31",{"name":78,"class":48},"Xuanwu Hospital, Beijing"]