Effectiveness and Adverse-effect Switch Evaluation of Xanomeline and Trospium Chloride (KarXT)
← catalyst calendarNCT07379827 · readout in 670 d
Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.
Phase
—
Status
Recruiting
Study type
Observational
Enrollment
1,500estimated
Sites
55
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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-02-26 | actual | When the study began enrolling |
| Primary completion | 2028-06-20 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2028-06-20 | estimated | The whole study's end, after follow-up |
| First posted | 2026-02-02 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-19 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Schizophrenia
Intervention
- Drug: Xanomeline and trospium chloride (KarXT)
Primary outcome
what the primary-completion date above is the date OFTreatment titration and switch regimens as described by the prescribing clinician
measured Baseline and up to 20 weeks
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