A Study to Evaluate the Long-term Efficacy and Safety of KarXT + KarX-EC for Agitation in Alzheimer's Disease (ADAGIO-3)
Sponsored by Bristol-Myers Squibb
About this study
The purpose of this study is to evaluate the long-term efficacy and safety of combined formulation of xanomeline tartrate/trospium chloride in an immediate release (IR) capsule (KarXT) and xanomeline enteric capsules (KarX-EC) in participants with agitation associated with Alzheimer's Disease who completed the parent studies CN012-0023 or CN012-0024.
Where this study is enrolling (9)
- I'm interested
Imaging Endpoints
Scottsdale, Arizona
- Call 786-616-9853
Nuovida Research Center
Miami, Florida
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- Call 386-304-7070
Progressive Medical Research
Port Orange, Florida
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- Call 786-681-4959
Hope Research Network - Miami
Virginia Gardens, Florida
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- Call 813-251-1800
IPTB Clinical Research
Tampa, Florida
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Show all 9 locations
- Call 413-281-0577
Boston Center for Memory
Newton, Massachusetts
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- Call 760-758-2222
Redbird Research
Las Vegas, Nevada
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- Call 252-515-0050
West Clinical Research
Morehead City, North Carolina
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- Call 972-782-2405
Epic Medical Research, LLC - Carrolton
Carrollton, Texas
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Who can participate
Inclusion criteria
- ✓Participants must have completed study CN012-0023 or CN012-0024 per protocol.
- ✓Participants must have an identified caregiver who has sufficient contact (approximately 8 hours over a week).
Exclusion criteria
- ✕Participants must not have clinically significant cardiovascular (eg, untreated or unstable hypertension, clinically significant tachycardia), pulmonary, renal, hematologic, GI, endocrine, immunologic, dermatologic, neurologic, or oncologic disease or any other condition that, in the opinion of the investigator, would jeopardize the safety of the participant or the validity of the study results.
- ✕Other protocol-defined Inclusion/Exclusion criteria apply.
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Trial data sourced from ClinicalTrials.gov.