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City","23561",{"type":51,"coordinates":1185},[1186,1187],121.45703,25.06199,{"lat":1187,"lon":1186},{"facility":1190,"status":67,"city":1191,"state":28,"zip":1192,"country":1169,"cosmosGeoPoint":1193,"geoPoint":1197,"contacts":28},"National Cheng Kung University Hospital","Tainan","704",{"type":51,"coordinates":1194},[1195,1196],120.21333,22.99083,{"lat":1196,"lon":1195},{"facility":1199,"status":45,"city":1200,"state":28,"zip":1201,"country":1169,"cosmosGeoPoint":1202,"geoPoint":1206,"contacts":28},"National Taiwan University Hospital","Taipei","10002",{"type":51,"coordinates":1203},[1204,1205],121.52639,25.05306,{"lat":1205,"lon":1204},{"type":1208,"investigatorFullName":28,"investigatorTitle":28,"investigatorAffiliation":28,"oldNameTitle":28,"oldOrganization":28},"SPONSOR","100528354",false,"NCT06159673","ACP-204 in Adults With Alzheimer's Disease Psychosis","A Master Protocol for Three Independent, Seamlessly Enrolling, Double-blind, Placebo-controlled Efficacy and Safety Studies of ACP-204 in Adults With Alzheimer's Disease Psychosis","Inclusion Criteria:\n\n* Is male or female and ≥55 and ≤95 years of age living in the community or in an institutionalized setting\n* Meets clinical criteria for possible or probable AD based on the 2011 National Institute on Aging-Alzheimer Association (NIA-AA) criteria\n* Meets the revised criteria for psychosis in major or mild neurocognitive disorder established by the International Psychogeriatrics Association (IPA)\n* Has either blood-based biomarker or documented evidence (e.g. positron emission tomography, cerebrospinal fluid biomarker) indicating amyloid plaque deposition and neuropathologic change consistent with AD\n* Has a prior magnetic resonance imaging or computed tomography scan of the brain that is consistent with the diagnosis of AD\n* Meets revised criteria for psychosis in major or mild neurocognitive disorder as per International Psychogeriatrics Association\n* MMSE score ≥6 and ≤24\n* Psychotic symptoms for at least 2 months\n* Lives in a stable place of residence and there are no plans to change living arrangements\n* Has a designated study partner\u002Fcaregiver\n* Able to complete all study visits with a study partner\u002Fcaregiver\n* Must be on a stable dose of cholinesterase inhibitor or memantine, if applicable\n\nExclusion Criteria:\n\n* Requires treatment with a medication prohibited by the protocol\n* Is in hospice and receiving end-of-life palliative care, or has become bedridden\n* Requires skilled nursing care\n* Psychotic symptoms that are primarily attributable to delirium, substance abuse, or a medical or psychiatric condition other than dementia\n* Known history of cerebral amyloid angiopathy, epilepsy, central nervous system neoplasm, or unexplained syncope\n* Atrial fibrillation\n* Symptomatic orthostatic hypotension\n* Protocol-defined exclusionary clinical laboratory findings\n* Treatment with anti-tau therapy or donanemab within 2 months prior to Screening\n\nAdditional inclusion\u002Fexclusion criteria apply. Subjects will be evaluated at screening to ensure that all criteria for study participation are met.","ALL","55 Years","95 Years",{"count":1219,"type":1220},1074,"ESTIMATED","INTERVENTIONAL",[1223,1224],"PHASE2","PHASE3","This is a master protocol for 3 independent, seamlessly enrolling, multicenter, randomized, double-blind, placebo-controlled, parallel-group studies in patients with ADP\n\n* Substudy 1 (Phase 2) will evaluate efficacy and dose response of ACP-204 30 and 60 mg vs placebo. This substudy will be initiated first.\n* Substudies 2A and 2B (both: Phase 3) will be confirmatory studies of either both doses (ACP-204 30 and 60 mg, respectively) or a single dose from Part 1 vs placebo. Substudies 2A and 2B will be performed independently of each other and will commence after enrollment of Part 1.\n\nAll 3 substudies will be analyzed independently of each other.\n\nEach substudy individually will consist of a screening period (up to 49 days); a double-blind treatment period (6 weeks); a safety follow-up period (30 days) for patients not rolling over into an open-label extension study; and vital status follow-up (for patients who terminated their substudy early).",[1227],"Alzheimer's Disease Psychosis",[1229,1230,1231],"Alzheimer's disease psychosis","Hallucinations","Delusions","2026-06-15",{"date":1234,"type":1235},"2026-06-16","ACTUAL",{"date":1237,"type":1235},"2023-11-14",{"date":1239,"type":1220},"2028-02",{"name":5,"class":6},145]