Relapse Prevention Trial Evaluating KarXT Treatment in Schizophrenia
Karuna Therapeutics, Inc., a Bristol Myers Squibb company · NCT07686263
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 3
- Target enrollment
- 472
- US sites recruiting
- 7
- Study start
- August 20, 2026
- Record last updated
- September 28, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of the study is to evaluate the relapse prevention of KarXT in the treatment of participants with Schizophrenia
Being studied: Xanomeline/Trospium Chloride; Placebo
Conditions: Schizophrenia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Participant must have a primary diagnosis of schizophrenia for at least 1 year established by a comprehensive psychiatric evaluation based on the DSM-5-TR (American Psychiatric Association 2022) criteria and confirmed by MINI for Psychotic Disorder Studies version 7.0.2 at screening.
- Participant must have experienced hospitalization for schizophrenia within 1 year from the screening date.
- Participant must be experiencing residual schizophrenia symptoms and have a PANSS total score ≥70 to ≤ 110 at screening and Day -1.
- Participant much have a PANSS Score of ≥ 4 (moderate or greater) on ≥ 2 of the following Positive Scale (P) items at screening and Day -1:
- Item 1 (P1; delusions)
- Item 2 (P2; conceptual disorganization)
- Item 3 (P3; hallucinatory behavior)
- Item 6 (P6; suspiciousness/persecution)
- Participant must have a CGI-S score of ≥ 4 at screening and Day -1
- Participant must have a BMI ≥ 18 and ≤ 40 kg/m2.
Exclusion Criteria
- Participant must not have any primary DSM-5 disorder other than schizophrenia within 12 months before screening
- Participants must not have a newly diagnosed or are experiencing their first treated episode of psychosis or schizophrenia.
- Participant must not have a risk of suicidal behavior as determined by the Investigator's clinical assessment and/or Columbia-suicide Severity Rating Scale (C-SSRS).
- Participant must not have had psychiatric hospitalization(s) for more than 30 days (cumulative) within the 6 months before screening.
- Participant must not have a history of treatment resistance to schizophrenia medications
- Participant must not have decrease in PANSS total score (floor adjusted) between screening and Day -1 of more than 20%.
- Other protocol-defined Inclusion/Exclusion criteria apply.
Recruiting US locations
Pillar Clinical Research - Bentonville
Bentonville, AR 72712
Site contact: Fayz Hudefi, Site 0154 · 479-367-2688
Pillar Clinical Research- Little Rock
Little Rock, AR 72204
Site contact: Leslie Smith, Site 0139 · 501-350-3285
Research Centers of America ( Hollywood )
Hollywood, FL 33024
Site contact: Edwin Gomez, Site 0145 · 954-604-3900
Health Synergy Clinical Research
West Palm Beach, FL 33407
Site contact: Mohammad Nisar, Site 0044 · 786-831-7303
Atlanta Center for Medical Research
Atlanta, GA 30331
Site contact: Elyssa Barron, Site 0166 · 404-881-5800
Pillar Clinical Research -Chicago
Chicago, IL 60641
Site contact: Roueen Rafeyan, Site 0056 · 312-865-6336
Pillar Clinical Research - Richardson
Richardson, TX 75080
Site contact: Scott Bartley, Site 0133 · 214-396-4844
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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