Korea Post Marketing Surveillance (PMS) Study of Talzenna®
← catalyst calendarNCT04982848 · readout in 805 d
Sponsored by Pfizer (industry) · PFE — their whole pipeline →.
Phase
—
Status
Not yet recruiting
Study type
Observational
Enrollment
600estimated
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 | 2027-06-01 | estimated | When the study began enrolling |
| Primary completion | 2028-11-01 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2028-11-01 | estimated | The whole study's end, after follow-up |
| First posted | 2021-07-29 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-11-18 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Breast Neoplasms
Intervention
- Drug: Talzenna
Primary outcome
what the primary-completion date above is the date OFIncidence of adverse events categorized according to physical organ and disease/symptom
measured From date of randomization until the 28 calendar days following the last administration of a drug under study
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