KarXT
DrugSpecified dose on specified days
Other names: BMS-986510, Xanomeline/Trospium Chloride
NCT Number: NCT06947941
The purpose of this study is to evaluate KarXT + KarX-EC as a treatment for psychosis associated with Alzheimer's disease.
Interested in participating?
Request Info55 year–90 year
All sexes
Interventional
Phase 3
Local Institution - 0020, Macquarie Park, New South Wales, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Specified dose on specified days
Other names: BMS-986510, Xanomeline/Trospium Chloride
Specified dose on specified days
Other names: BMS-986519, Xanomeline Enteric-coated
Specified dose on specified days
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
NPI-C Core Score includes assessment for hallucinations, delusions, agitation, and aggression domains
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
NPI-C Core Score: Caregiver Distress Scale includes assessment for hallucinations, delusions, agitation, and aggression domains
Time frame: Up to approximately Week 14
Responder rate is defined as improvement from baseline in NPI-C: H+D score ≥ 40%.
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Procholinergic symptoms include nausea, vomiting, and diarrhea.
Time frame: Up to approximately Week 14
Anticholinergic symptoms include dry mouth, constipation, urinary retention and blurred vision.
Time frame: Up to approximately Week 14
AESIs such as symptomatic orthostasis, syncope, urinary adverse events, and elevated liver enzymes will be evaluated.
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
This will be measured in males only.
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
This includes measuring of BP, supine or sitting and then standing after approximately 2 minutes, no later than approximately 3 minutes.
Time frame: Up to approximately Week 14
This includes measuring of HR, supine or sitting and then standing after approximately 2 minutes, no later than approximately 3 minutes.
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Time frame: Up to approximately Week 14
Contact information is provided by the study sponsor or research team.
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com, www.BMSStudyConnect.com
CONTACT
First line of the email MUST contain NCT # and Site #.
CONTACT
Bristol-Myers Squibb
Industry
A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate the Safety and Efficacy of KarXT + KarX-EC for the Treatment of Psychosis Associated With Alzheimer's Disease
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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