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Real-world Patient Characteristics, Treatment Patterns, and Healthcare Utilization Among KarXT Users

← catalyst calendar

NCT07571148

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
6,876actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-01-16actualWhen the study began enrolling
Primary completion2026-03-25actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-07-31estimatedThe whole study's end, after follow-up
First posted2026-05-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-06actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Schizophrenia

Intervention

  • Drug: KarXT (xanomeline and trospium)

Primary outcomes

what the primary-completion date above is the date OF
Number of all-cause and schizophrenia-related healthcare encounters per participant
measured Baseline and up to 6 months
Number of participants adherent to KarXT (proportion of days covered ≥80%)
measured Baseline and up to 6 months
Time to discontinuation of KarXT
measured Baseline and up to 6 months
KarXT initial dose (index dose)
measured Baseline
Number of of participants with dose increases or decreases
measured Baseline and up to 6 months
Number of participants using concomitant antipsychotic and anticholinergic medications
measured Baseline and up to 6 months
Number of participants with comorbidities
measured Baseline and up to 6 months
Number of participants with gastrointestinal adverse events
measured Baseline and up to 6 months
Number of participants with documented schizophrenia symptoms
measured Baseline and up to 6 months

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