A Study to Evaluate KarXT as a Treatment for Psychosis Associated With Alzheimer's Disease (ADEPT-4)
Sponsored by Karuna Therapeutics, Inc., a Bristol Myers Squibb company
About this study
The purpose of this study is to evaluate the safety and efficacy of KarXT in adult participants with mild to severe Alzheimer's Disease (AD) with moderate to severe psychosis related to AD.
Where this study is enrolling (43)
- Call 480-926-0644
Gilbert Neurology Partners - PLLC - Avacare
Gilbert, Arizona
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- Call 602-839-6900
Banner Alzheimer's Institute
Phoenix, Arizona
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- Call 714-999-6688
Advanced Research Center, Inc.
Anaheim, California
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- Call 909-488-9116
Inland Psychiatric Medical Group (IPMG)-Chino
Chino, California
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- Call 323-442-3715
USC - The Memory and Aging Center (MAC) - Alzheimer Disease Research Center (ADRC)
Los Angeles, California
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Show all 43 locations
- Call 860-790-7354
University of Connecticut Health Center
Farmington, Connecticut
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- Call 407-823-8421
Nova Psychiatry
Orlando, Florida
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- Call 352-775-1000
Charter Research
The Villages, Florida
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- Call 305-819-2909
Envision Trials LLC
Bonita Springs, Florida
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- Call 386-278-8000
Arrow Clinical Trials
Daytona Beach, Florida
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- Call 941-436-6838
Aqualane Clinical Research
Naples, Florida
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- Call 407-654-2724
Sensible HealthCare, LLC
Ocoee, Florida
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- Call 407-440-4493
Combined Research Orlando Phase I-IV LLC
Orlando, Florida
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- Call 813-300-3300
Guardian Angel Research
Tampa, Florida
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- Call 813-251-1800
Interventional Psychiatry of Tampa Bay
Tampa, Florida
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- Call 561-845-0500
Premiere Research Institute at Palm Beach Neurology, PA
West Palm Beach, Florida
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- I'm interested
Agile Clinical Research Trials, LLC
Atlanta, Georgia
- Call 508-925-7403
Boston Neuro Research Center
North Dartmouth, Massachusetts
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- Call 413-305-1142
Elixia Health - Springfield - Elixia - PPDS
Springfield, Massachusetts
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- Call 617-636-3202
Tufts Medical Center - 800 Washington St - PPDS
Boston, Massachusetts
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- Call 617-855-2136
McLean Hospital
Belmont, Massachusetts
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- Call 412-916-2425
Neurobehavioral Medicine Group (NBMG)
Bloomfield Township, Michigan
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- Call 601-420-5810
Precise Research Centers
Flowood, Mississippi
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- Call 314-594-7785
Tekton Research, LLC - Saint Louis Psychiatry - PPDS
St Louis, Missouri
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- Call 732-341-9500
Advanced Memory Research Institute - CenExel - PPDS
Toms River, New Jersey
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- Call 617-636-5000
SUNY Upstate Medical University
Syracuse, New York
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- Call 845-674-9398
Mid Hudson Medical Research PLLC
New Windsor, New York
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- Call 516-239-1800
Five Towns Neurology, PC
Woodmere, New York
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- Call 252-515-0050
West Clinical Research
Morehead City, North Carolina
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- Call 336-235-0991
Triad Clinical Trials - 515 College Rd
Greensboro, North Carolina
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- Call 704-364-4000
AMC Research, LLC - Flourish - PPDS
Matthews, North Carolina
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- Call 216-444-8897
Insight Clinical Trials LLC - Independence
Independence, Ohio
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- Call 614-293-4560
Ohio State University
Columbus, Ohio
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- Call 405-317-5783
The Rivus Wellness & Research Institute
Oklahoma City, Oklahoma
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- Call 714-456-7002
Alzheimer's Disease and Memory Disorders Center at Rhode Island Hospital
Providence, Rhode Island
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- Call 615-322-4967
Vanderbilt Psychiatric Hospital
Nashville, Tennessee
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- Call 512-407-8628
Senior Adults Specialty Research
Austin, Texas
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- Call 972-777-6956
Epic Medical Research LLC - DeSoto
DeSoto, Texas
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- Call 210-567-8229
Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases
San Antonio, Texas
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- Call 972-717-6262
University Hills Clinical Research - 102 Decker Ct
Irving, Texas
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- Call 915-974-2200
Advanced Neuro Research Center - El Paso
El Paso, Texas
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- Call 703-717-7755
Conquest Research, LLC - Virginia - Vienna
Vienna, Virginia
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- Call 425-453-0404
Northwest Clinical Research Center
Bellevue, Washington
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Who can participate
Inclusion criteria
- ✓Patients who are 55 to 90 years of age, inclusive, at the time of Screening (Visit 1).
- ✓Patients who are diagnosed with AD based on the 2024 revised criteria for diagnosis and staging of AD: Alzheimer's Association Workgroup.
- ✓Patient must have a magnetic resonance imaging (MRI) or computed tomography (CT) scan of the brain (completed within the past 5 years) taken during or subsequent to the onset of dementia to rule out other central nervous system (CNS) disease that could account for the dementia syndrome, eg, major stroke, neoplasm, subdural hematoma.
- ✓Patient must have a history of psychotic symptoms (meeting International Psychogeriatric Association criteria) for at least 2 months prior to Screening (Visit 1) (participants may or may not have symptoms of agitation).
Exclusion criteria
- ✕\- Patients will not be able to participate if they have:
- ✕i) Psychotic symptoms that are primarily attributable to a condition other than the AD causing the dementia, eg, schizophrenia, schizoaffective disorder, delusional disorder, or mood disorder with psychotic features.
- ✕ii) History of major depressive episode with psychotic features during the 12 months prior to Screening, or history of bipolar disorder, schizophrenia, or schizoaffective disorder.
- ✕iii) Patients are not able to participate if they have certain safety concerns, including certain laboratory test irregularities.
- ✕\* Other protocol-defined Inclusion/Exclusion criteria apply.
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.