A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of KarXT + KarX-EC for the Treatment of Cognitive Impairment Associated With Mild to Moderate Alzheimer's Disease (MINDSET 2)

ReclutandoFase 3ClinicalTrials.gov

ID: NCT06976203Tipo: INTERVENTIONALInicio: 21 de jul de 2025Fin estimado: 23 de feb de 2029

Traducción no disponible, mostrando original

Resumen

The purpose of this study is to evaluate the efficacy and safety of KarXT + KarX-EC for cognitive impairment in Alzheimer's Disease

Elegibilidad

Edad mínima: 60 YearsEdad máxima: 85 YearsSexo: ALL

Criterios de inclusión

Participants must have a confirmed diagnosis of Alzheimer's disease (AD), specifically at the mild (stage 4) or moderate (stage 5) dementia stages, as defined by the National Institute on Aging and Alzheimer's Association (NIA-AA) core clinical criteria. The diagnosis of AD pathology must be confirmed through the 2024 revised NIA-AA Workgroup criteria using a stepwise diagnostic approach.
Participants must have an Mini-Mental State Examination (MMSE) score ranging from 12 through 22, inclusive, at the time of screening.
Participants must have a designated caregiver who maintains adequate contact (around 10 hours per week or more) and is willing to attend all study visits. The caregiver must also be responsible for reporting on the participant's condition, overseeing medication compliance, and consenting to their involvement in both their own and the participant's study-related activities.
Participants on acetyl choline esterase inhibitors (AChEIs) and/or memantine, must have been on a stable dosage for at least 12 weeks prior to screening, and agree to maintain this stable dose for the study duration.

Criterios de exclusión

Participants must not present with any significant or severe medical conditions that could compromise their safety, the ability to comply with or complete the study, or the integrity of the study results. This includes any grade of hepatic impairment, urinary retention, active biliary disease, moderate-severe renal impairment (eGFR of \<50 mL/min), and unstable hypertension or tachycardia.
Participants must not have any primary psychiatric diagnoses such as major depression, schizoaffective disorder, or bipolar disorder, and those with severe psychiatric symptoms that could complicate the interpretation of treatment effects, impair cognitive assessment, or impact study completion.
Participants must not have a history of schizophrenia or other chronic psychosis, as well as those who have previously been exposed to KarXT or are currently undergoing treatment with disease-modifying anti-amyloid therapies for AD within the past 6 months prior to screening.
Participants must not have significant pathological findings on brain magnetic resonance imaging (MRI) at screening that could affect safety or interfere with study procedures.

Intervenciones

drug

KarXT

Specified dose on specified days

drug

KarX-EC

Specified dose on specified days

other

Placebo

Specified dose on specified days

Ubicaciones

Local Institution - 0029

ABB, Buenos Aires F.D., Argentina

Site 0029

NOT_YET_RECRUITING

Centro Médico Luquez

Córdoba, Córdoba Province, Argentina

Juan Luquez, Site 0027 · +5493517481586

RECRUITING

Local Institution - 0025

Buenos Aires, Argentina

Site 0025

NOT_YET_RECRUITING

CEN Centro Especializado en Neurociencias

Córdoba, Argentina

Hernan Ruggeri, Site 0028 · 93515339477

RECRUITING

Local Institution - 0030

Córdoba, Argentina

Site 0030

NOT_YET_RECRUITING

Local Institution - 0026

Mendoza, Argentina

Site 0026

NOT_YET_RECRUITING

Patrocinadores

PrincipalBristol-Myers Squibb

Contactos

BMS Clinical Trials Contact Center www.BMSClinicalTrials.com

CONTACT

Clinical.Trials@bms.com 855-907-3286

First line of the email MUST contain NCT # and Site #.

CONTACT

Aviso: La información de este ensayo proviene de fuentes públicas y tiene carácter exclusivamente informativo. No constituye asesoramiento médico, regulatorio ni de ningún otro tipo. Las traducciones son automatizadas y no poseen validez oficial. Consultá siempre con un profesional de la salud. Ver Términos de Uso.

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