KarXT
DrugSpecified dose on specified days
Other names: BMS-986510
NCT Number: NCT07061288
A study to evaluate the safety, tolerability, and PK of an injectable form of KarXT in participants with schizophrenia
Interested in participating?
Request Info18 year–55 year
All sexes
Interventional
Phase 1
Collaborative Neuroscience Research, LLC, Los Alamitos, California, United States
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
Time frame: Up to 3 weeks
Time frame: Up to 3 weeks
Time frame: Up to 3 weeks
Time frame: Up to 15 weeks
Time frame: Up to 15 weeks
Time frame: Up to 15 weeks
Time frame: Up to 15 weeks
Time frame: Up to 15 weeks
Time frame: Up to 15 weeks
Time frame: Up to 15 weeks
Time frame: Up to 15 weeks
Time frame: Up to 3 weeks
Time frame: Up to 3 weeks
Time frame: Up to 3 weeks
Contact information is provided by the study sponsor or research team.
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
CONTACT
First line of the email MUST contain NCT # and Site #.
CONTACT
Bristol-Myers Squibb
Industry
An Open-label, Phase 1, Dose-Finding Study to Characterize the Safety, Tolerability, and Pharmacokinetics of a Long-Acting Injectable KarXT Formulation in Participants With Schizophrenia
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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