Mavacamten Post-marketing Surveillance in Patients With Obstructive Hypertrophic Cardiomyopathy in Japan
← catalyst calendarNCT07383025 · readout in 1,198 d
Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.
Phase
—
Status
Recruiting
Study type
Observational
Enrollment
200estimated
Sites
1
Country
Japan
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 | 2025-05-21 | actual | When the study began enrolling |
| Primary completion | 2029-11-30 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2029-11-30 | estimated | The whole study's end, after follow-up |
| First posted | 2026-02-03 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-02-03 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Obstructive Hypertrophic Cardiomyopathy (oHCM)
Intervention
- Drug: Mavacamten
Primary outcomes
what the primary-completion date above is the date OFIncidence of adverse events (AEs) and/or serious AEs (SAEs)
measured Up to 52 weeks
Actions taken after adverse events (AEs) and/or serious AEs (SAEs)
measured Up to 52 weeks
Outcome of adverse events (AEs) and/or serious AEs (SAEs)
measured Up to 52 weeks
Permalink · BMY's whole pipeline · Catalyst calendar · Every registered study · What changed