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Patterns of Care and Outcomes in Locally Recurrent Inoperable or Metastatic Triple-Negative Breast Cancer

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NCT07092254

Sponsored by Daiichi Sankyo (industry) · 4568.T — their whole pipeline →.

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
760estimated
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
Start2025-09-01actualWhen the study began enrolling
Primary completion2025-11-28actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-09-04estimatedThe whole study's end, after follow-up
First posted2025-07-29actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-17actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Triple Negative Breast Cancer

Intervention

  • Drug: No drug

Primary outcomes

what the primary-completion date above is the date OF
Treatment sequencing before the diagnosis of advanced, metastatic TNBC (i.e., all treatments received for early TNBC if initially diagnosed with earlier-stage disease)
measured From date of initial diagnosis of early TNBC (if applicable) until diagnosis date of advanced, metastatic TNBC, up to approximately 15 months
Treatment sequencing on or after the diagnosis date for advanced, metastatic TNBC
measured From date of initial diagnosis of advanced, metastatic TNBC until end of follow-up, up to approximately 15 months
Real-world disease-free interval (rwDFI)
measured From the completion of treatment with curative intent (either date of breast tumor surgery or date of last dose of systemic therapy (whichever occurred last) and the first local or distant disease recurrence date, up to approximately 15 months
Clinician-defined real-world progression-free survival (rwPFS)
measured From the start of each line of therapy until end of follow up, up to approximately 15 months
Overall survival
measured From the start of each line of therapy until end of follow-up, up to approximately 15 months
Occurrence of clinical events of interest
measured From the start of each line of therapy until end of follow-up, up to approximately 15 months

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