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RecruitingPhase 3

Relapse Prevention Trial Evaluating KarXT Treatment in Schizophrenia

Karuna Therapeutics, Inc., a Bristol Myers Squibb company · NCT07686263

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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 #.
Relapse Prevention Trial Evaluating KarXT Treatment in Schizophrenia (NCT07686263) | Bored Studies