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6BE",{"type":52,"coordinates":728},[729,730],-1.61396,54.97328,{"lat":730,"lon":729},{"facility":361,"status":46,"city":733,"state":28,"zip":734,"country":684,"cosmosGeoPoint":735,"geoPoint":739,"contacts":28},"Salford","M6 8HD",{"type":52,"coordinates":736},[737,738],-2.29042,53.48771,{"lat":738,"lon":737},{"facility":361,"status":46,"city":741,"state":28,"zip":742,"country":684,"cosmosGeoPoint":743,"geoPoint":747,"contacts":28},"Southampton","SO16 6YD",{"type":52,"coordinates":744},[745,746],-1.40428,50.90395,{"lat":746,"lon":745},{"type":749,"investigatorFullName":28,"investigatorTitle":28,"investigatorAffiliation":28,"oldNameTitle":28,"oldOrganization":28},"SPONSOR","100600209",false,"NCT07094516","A Clinical Trial to Learn About the Effects of VHB937 in People With Early Alzheimer's Disease","A Randomized, Placebo-controlled, Parallel Group, 72-week Study to Evaluate the Efficacy and Safety of VHB937 in Participants With Early Alzheimer's Disease Followed by an Extension","Key Inclusion Criteria\n\n* Male or female participants 50 to 85 years of age\n* Diagnosis of Mild Cognitive Impairment (MCI) due to AD or mild AD\n* Clinical Dementia Rating (CDR) Global score of 0.5 or 1.0\n* Confirmation of AD based on cerebral spinal fluid (CSF) biomarkers or amyloid PET imaging\n* Reliable study partner who can accompany the participant at study visits\n* If on symptomatic AD treatment (AChEIs\u002Fmemantine), on a stable dose prior to starting study treatment\n\nKey Exclusion Criteria\n\n* Dementia due to a condition other than AD, including but not limited to, frontal temporal dementia, Parkinson's disease, dementia with Lewy bodies, Huntington disease, vascular dementia.\n* History or current diagnosis of cardiac conditions or ECG abnormalities indicating significant risk of safety for participants in the study\n* Transient ischemic attacks (TIA) or stroke occurring within 12 months\n* Clinical evidence of liver or renal disease\u002Finjury\n* Current major depressive episode that is not adequately controlled, history of schizophrenia, other chronic psychosis\n* Significant neurological disease other than dementia (e.g. serious brain infection, traumatic brain injury, multiple concussions, epilepsy or recurrent seizures\n* Presence of suicidal ideation within 6 months or suicidal behavior within 2 years before Screening\n* Presence of cancer, HIV, Hep B, Hep C, uncontrolled thyroid disease, uncontrolled diabetes\n* Taking any prohibited medications\n\nOther protocol-defined inclusion\u002Fexclusion criteria may apply","ALL","50 Years","85 Years",{"count":760,"type":761},407,"ESTIMATED","INTERVENTIONAL",[764],"PHASE2","This is a multicentre, randomized, double-blind, placebo-controlled, parallel group Phase II study to evaluate the efficacy and safety of VHB937 in participants with early AD followed by an Extension. The double-blind part is 72 weeks long, followed by an extension.",[767],"Alzheimer's Disease",[769,770,771,772],"Alzheimer's disease","AD","Dementia","Monoclonal Antibody","2026-06-25",{"date":775,"type":776},"2026-06-26","ACTUAL",{"date":778,"type":776},"2025-08-07",{"date":780,"type":761},"2030-12-31",{"name":37,"class":6},74]