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Evaluation of Treatment Satisfaction and KarXT Utilization Registry (RESKU)

Evaluation of Treatment Satisfaction and KarXT Utilization Registry (RESKU)

Recruiting
18 years and older
All
Phase N/A

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Overview

The purpose of this study is to understand treatment preference and satisfaction among adults with schizophrenia in the United States who are prescribed xanomeline and trospium chloride (X/T) therapy

Eligibility

Inclusion Criteria:

  • Aged ≥18 years at index date.
  • Have a confirmed diagnosis of schizophrenia before index date.
  • Receipt of an initial prescription order for xanomeline and trospium chloride (XT) and plan to fill and initiate such therapy.
  • Provide a signed and dated Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved written informed consent form (ICF) in accordance with regulatory, local, and institutional guidelines.
  • Agree to use an electronic device to record, or provide paper entry of, patient-reported outcomes (in English or Spanish).
  • English or Spanish speaking.

Exclusion Criteria:

  • Participation in an interventional study within the last 30 days or plan to participate in such study at the time of eligibility screening.
  • Evidence of use of XT prior to time of eligibility screening.

Study details
    Schizophrenia

NCT07101094

Bristol-Myers Squibb

1 November 2025

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