Clinical Trials in the USA / NCT07101094
Recruiting
Observational
Evaluation of Treatment Satisfaction and KarXT Utilization Registry (RESKU)
NCT07101094 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Schizophrenia
Investigational drug(s) / intervention(s)
xanomeline and trospium chloride (X/T) therapy
xanomeline and trospium chloride (X/T) therapy: According to the product label
Study summary
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.
Primary outcome measure(s)
- Participant medication preference as assessed by the Preference of Medication (POM) questionnaire — Month 1, Month 3, Month 6
- Participant treatment satisfaction as assessed by the Medication Satisfaction Questionnaire (MSQ) — Baseline, Month 1, Month 3, Month 6
Trial sites (20)
| Facility | City | Region | Status |
|---|---|---|---|
| ATP Clinical Research - Costa Mesa | Orange | California | Recruiting |
| Lumos Clinical Research Center | San Jose | California | Recruiting |
| Local Institution - 0019 | Miami | Florida | Not Yet Recruiting |
| Evanston Hospital | Evanston | Illinois | Recruiting |
| The Johns Hopkins Hospital | Baltimore | Maryland | Recruiting |
| Local Institution - 0017 | Bel Air | Maryland | Withdrawn |
| Local Institution - 0004 | Catonsville | Maryland | Withdrawn |
| Local Institution - 0008 | Belmont | Massachusetts | Completed |
| Boston Medical Center | Boston | Massachusetts | Recruiting |
| Local Institution - 0011 | South Dartmouth | Massachusetts | Completed |
| Local Institution - 0020 | Grand Island | Nebraska | Not Yet Recruiting |
| Omaha Insomnia and Psychiatric Services | Omaha | Nebraska | Recruiting |
| Hackensack Meridian Health - Carrier Clinic | Belle Mead | New Jersey | Recruiting |
| Radial - Manhattan | New York | New York | Recruiting |
| New Dawn Psychiatric Services, PLLC | Kinston | North Carolina | Recruiting |
| New Dimension Group | Rose Hill | North Carolina | Recruiting |
| Westlake Brain Health | Westlake | Ohio | Recruiting |
| Continuum Health Providers | Fort Mill | South Carolina | Recruiting |
| Haracec Clinical Research | El Paso | Texas | Recruiting |
| C-Trilogy Outreach | Longview | Texas | Recruiting |
More Bristol-Myers Squibb trials in the USA
Other trials for the same condition
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52-week Open Label Safety-Tolerability Study
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07101094 on ClinicalTrials.gov ↗ ← All trials in the USA