A Study to Evaluate the Effect of KarXT on Urological Safety
Bristol-Myers Squibb · NCT07221877
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 4
- Target enrollment
- 60
- US sites recruiting
- 13
- Study start
- January 20, 2026
- Record last updated
- October 19, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to characterize the effect of KarXT on voiding dynamics and urological safety in participants with DSM-5 schizophrenia.
Being studied: Xanomeline/trospium chloride
Conditions: Schizophrenia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Male and Female participants (age 18 to 65 years of age, with a primary diagnosis of schizophrenia based on psychiatric evaluation (DSM-5) and confirmed by MINI (v 7.0.2).
- Participants must have a PANSS total score ≤ 80 and CGI-S score ≤ 4, at screening and baseline, and a BMI ≥18 and ≤ 40 kg/m2.
- Participants must be willing and able to discontinue all antipsychotic medications prior to the baseline visit and be willing and able to comply with protocol requirements.
Exclusion Criteria
- Participants with newly diagnosed schizophrenia, any other DSM-5 disorder diagnosed within the past 12 months, alcohol or drug use disorder within the past 12 months, history/presence of clinically significant disease or disorder that would jeopardize participant safety or validity of study results.
- Participants at risk for suicidal behavior, as well as individuals who are pregnant or breastfeeding, will be excluded from the study.
- Other protocol-defined Inclusion/Exclusion criteria apply
Recruiting US locations
Pillar Clinical Research- Little Rock
Little Rock, AR 72204
Site contact: Leslie Smith, Site 0017 · 501-350-3285
Clinical Innovations, Inc. dba CITrials
Bellflower, CA 90706
Site contact: Robert Bota, Site 0007 · 562-748-4999
CenExel CNS - Garden Grove
Garden Grove, CA 92845
Site contact: David Walling, Site 0006 · 714-799-7799
ATP Clinical Research
Orange, CA 92866
Site contact: Gustavo Alva, Site 0016 · 949-354-5353
Collaborative Neuroscience Research, LLC
Torrance, CA 90504
Site contact: Lara Shirikjian, Site 0019 · 310-523-4200
Health Synergy Clinical Research
Boynton Beach, FL 33426
Site contact: Mohammad Nisar, Site 0004 · 786-831-7303
Innovative Clinical Research
Lauderhill, FL 33319
Site contact: Rishi Kakar, Site 0003 · 786-512-4106
Uptown Research Institute
Chicago, IL 60640
Site contact: John Sonnenberg, Site 0005 · 773-968-9868
Pillar Clinical Research -Chicago
Chicago, IL 60641
Site contact: Roueen Rafeyan, Site 0010 · 312-865-6336
IMA Clinical Research Las Vegas
Las Vegas, NV 89102
Site contact: Mustafa Rawaf, Site 0013 · 702-527-7401
Hassman Research Institute Marlton Site
Marlton, NJ 08053
Site contact: Elan Cohen, Site 0002 · 267-981-8911
Adams Clinical Philadelphia
Philadelphia, PA 19104
Site contact: Cassie Blanchard, Site 0014 · 631-252-0769
Adams Clinical Dallas
DeSoto, TX 75115
Site contact: Benji Kurian, Site 0015 · 214-497-3151
Study contacts (from the official record)
- BMS Clinical Trials Contact Center www.BMSClinicalTrials.com · 855-907-3286 · Clinical.Trials@bms.com
- First line of the email MUST contain NCT # and Site #.
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