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NCT07061288RecruitingPhase 1

A Study to Evaluate the Safety, Tolerability, and PK of an Injectable Form of KarXT

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

Source: ClinicalTrials.gov · Last updated 2 Sept 2026

Brief summary (registry, in English)

A study to evaluate the safety, tolerability, and PK of an injectable form of KarXT in participants with schizophrenia

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
131 (estimated)
First submitted
2 Jul 2025
Start date
3 Sept 2025
Primary completion date
21 Jun 2027
Lead sponsor
Bristol-Myers Squibb
NCT number
NCT07061288

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 131
  • From 3 Sept 2025 to the primary completion date, 21 Jun 2027
  • 8 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Participants must not have any other DSM-5-TR disorder diagnosed within the past 12 months, such as major depressive disorder or bipolar disorder.
  • Participants must not have a history of alcohol or drug use disorder within the past 12 months or those with clinically significant disease or disorder that would jeopardize their safety or affect the validity of study results.

Other

  • Participants must not have newly diagnosed schizophrenia or a first treated episode of schizophrenia.
  • Participants must not be at risk for suicidal behavior.
  • Female participants must not be pregnant or breastfeeding.
  • Other protocol-defined Inclusion/Exclusion criteria apply.

Who the study is looking for

  • Participants must have a primary diagnosis of schizophrenia, as confirmed by psychiatric evaluation based on Diagnostic and Statistical Manual of Mental Disorders (5th Edition, Text Revision) (DSM-5-TR) criteria and Mini International Neuropsychiatric Interview (MINI) (version 7.0.2).
  • Participants must have a Positive and Negative Syndrome Scale (PANSS) total score ≤ 80 and a Clinical Global Impression - Severity (CGI-S) score ≤ 4 at both screening and baseline.
  • Participants must have a body mass index (BMI) between 18 and 40 kg/m².
  • Participants should be willing and able, as determined by the investigator, to discontinue all antipsychotic medications prior to the baseline visit and must be able to comply with all protocol requirements.

Age in the registry: 18 years to 55 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Atlanta Center for Medical Research
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting
Community Clinical Research
Coordinator of this site? Confirm its status
AustinUnited StatesRecruiting
Uptown Research Institute
Coordinator of this site? Confirm its status
ChicagoUnited StatesRecruiting
CenExel iResearch, LLC
Coordinator of this site? Confirm its status
DecaturUnited StatesRecruiting
Research Centers of America ( Hollywood )
Coordinator of this site? Confirm its status
HollywoodUnited StatesRecruiting
Collaborative Neuroscience Research, LLC
Coordinator of this site? Confirm its status
Los AlamitosUnited StatesRecruiting
Hassman Research Institute Marlton Site
Coordinator of this site? Confirm its status
MarltonUnited StatesRecruiting
Innovative Clinical Research, Inc.
Coordinator of this site? Confirm its status
Miami LakesUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.