ACP-204 in Adults With Alzheimer's Disease Psychosis

A vizsgálat adatai

Ki végzi

ACADIA Pharmaceuticals Inc.

Azonosító

NCT06159673EU 2023-507325-42-00

A regiszteradat frissítve

2026. november 5.

Eredeti leírás

This is a master protocol for 3 independent, seamlessly enrolling, multicenter, randomized, double-blind, placebo-controlled, parallel-group studies in patients with ADPA teljes eredeti leírásKevesebb

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

This is a master protocol for 3 independent, seamlessly enrolling, multicenter, randomized, double-blind, placebo-controlled, parallel-group studies in patients with ADP

* 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. * 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.

All 3 substudies will be analyzed independently of each other.

Each 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).

Bevonási feltételek: Is male or female and ≥55 and ≤95 years of age living in the community or in an institutionalized setting; Meets clinical criteria for possible or probable AD based on the 2011 National Institute on Aging-Alzheimer Association (NIA-AA) criteria; Meets the revised criteria for psychosis in major or mild neurocognitive disorder established by the International Psychogeriatrics Association (IPA); 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; Has a prior magnetic resonance imaging or computed tomography scan of the brain that is consistent with the diagnosis of AD; Meets revised criteria for psychosis in major or mild neurocognitive disorder as per International Psychogeriatrics Association; MMSE score ≥6 and ≤24; Psychotic symptoms for at least 2 months; Lives in a stable place of residence and there are no plans to change living arrangements; Has a designated study partner/caregiver; Able to complete all study visits with a study partner/caregiver; Must be on a stable dose of cholinesterase inhibitor or memantine, if applicable.

Kizáró feltételek: Requires treatment with a medication prohibited by the protocol; Is in hospice and receiving end-of-life palliative care, or has become bedridden; Treatment with anti-tau therapy or donanemab within 2 months prior to Screening; Additional inclusion/exclusion criteria apply. Subjects will be evaluated at screening to ensure that all criteria for study participation are met; Psychotic symptoms that are primarily attributable to delirium, substance abuse, or a medical or psychiatric condition other than dementia; Known history of cerebral amyloid angiopathy, epilepsy, central nervous system neoplasm, or unexplained syncope; Protocol-defined exclusionary clinical laboratory findings; Requires skilled nursing care; Atrial fibrillation; Symptomatic orthostatic hypotension.

ClinicalTrials.gov NCT06159673 · EU CTIS 2023-507325-42-00