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Tracks how adults with schizophrenia feel about xanomeline and trospium treatment

Studies treatment preference and satisfaction in adults with schizophrenia taking xanomeline and trospium.

Key facts

Who runs it
Bristol-Myers Squibb
Where
Baltimore, Bel Air, Belle Mead, Belmont, Boston, Catonsville, El Paso, Evanston, Fort Mill, Grand Island, Kinston, Longview, Miami, New York, Omaha, Orange, Rose Hill, San Jose, South Dartmouth, and Westlake, United StatesSee the 20 sites
Trial code
Registry title
Evaluation of Treatment Satisfaction and KarXT Utilization Registry (RESKU)
Status
Recruiting
People taking part
300 people, planned
Started
22 Sept 2025
Expected to end
14 May 2029
Type of study
Observational
Treatments tested
  • xanomeline and trospium chloride (X/T) therapy
Record updated
30 September 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with schizophrenia in the United States who have been prescribed xanomeline and trospium chloride (X/T) and plan to start it.

Age
18 years or older
Sex
All sexes can join
Disease stage
A confirmed diagnosis of schizophrenia before the start date
Earlier treatment
Must have a first prescription for xanomeline and trospium chloride (XT) and plan to fill and start it. Must not have used XT before screening.

Main reasons for not taking part

  • Took part in an interventional study in the last 30 days
  • Plans to take part in an interventional study at the time of screening
  • Has already used XT before screening
  • Cannot give signed written informed consent
  • Does not speak English or Spanish

The registry criteria, word for word

Show all 8 criteriaShow less

Who can take part

  • 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

Who cannot take part

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

Where in United States

  • The Johns Hopkins HospitalBaltimore, United StatesContact: Frederick Nucifora, Site 0007Taking people
  • Bel Air, MarylandHospital not named in the registryNo longer taking part
  • Hackensack Meridian Health - Carrier ClinicBelle Mead, United StatesContact: Stacy Doumas, Site 0001Taking people
  • Belmont, MassachusettsHospital not named in the registryNo longer taking part
  • Boston Medical CenterBoston, United StatesContact: Hannah Brown, Site 0002Taking people
  • Catonsville, MarylandHospital not named in the registryNo longer taking part
  • Haracec Clinical ResearchEl Paso, United StatesContact: Aghaegbulam Uga, Site 0012Taking people
  • Evanston HospitalEvanston, United StatesContact: Joshua Straus, Site 0003Taking people
  • Continuum Health ProvidersFort Mill, United StatesContact: Brian Mika, Site 0006Taking people
  • Grand Island, NebraskaHospital not named in the registryContact: Site 0020Not yet recruiting
  • New Dawn Psychiatric Services, PLLCKinston, United StatesContact: Punitha Rathnam, Site 0016Taking people
  • C-Trilogy OutreachLongview, United StatesContact: Tracy Hicks, Site 0013Taking people
  • Miami, FloridaHospital not named in the registryContact: Site 0019Not yet recruiting
  • Radial - ManhattanNew York, United StatesContact: Owen Muir, Site 0015Taking people
  • Omaha Insomnia and Psychiatric ServicesOmaha, United StatesContact: Vithya Selvaraj, Site 0005Taking people
  • ATP Clinical Research - Costa MesaOrange, United StatesContact: Gustavo Alva, Site 0009Taking people
  • New Dimension GroupRose Hill, United StatesContact: Constance Olatidoye, Site 0018Taking people
  • Lumos Clinical Research CenterSan Jose, United StatesContact: Sarbani Maitra, Site 0010Taking people
  • South Dartmouth, MassachusettsHospital not named in the registryNo longer taking part
  • Westlake Brain HealthWestlake, United StatesContact: Abdelrahman Abdelaziz, Site 0014Taking people

About the trial

What the trial wants to find out

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

The group in the trial

  • Participants receiving xanomeline and trospium chloride (X/T) therapy

    Treatment: xanomeline and trospium chloride (X/T) therapy

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Real-world Evaluation of Treatment Satisfaction and KarXT Utilization Registry (RESKU)
Plain-language title
Tracks how adults with schizophrenia feel about xanomeline and trospium treatmentGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Record updated
30 September 2026