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Real World-clinical Outcomes of Tucatinib, Trastuzumab, and Capecitabine Following Trastuzumab Deruxtecan (T-DXd) for the Treatment of HER2-positive Metastatic Breast Cancer.

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NCT06961331

Sponsored by Pfizer (industry) · PFE — their whole pipeline →.

Phase
Status
Completed
Study type
Observational
Enrollment
86actual
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
Start2025-05-07actualWhen the study began enrolling
Primary completion2025-09-25actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-09-25actualThe whole study's end, after follow-up
First posted2025-05-07actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-01-09actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Metastatic HER2+ Advanced Breast Cancer

Interventions

  • Drug: Tucatinib
  • Drug: Trastuzumab
  • Drug: Capecitabine

Primary outcomes

what the primary-completion date above is the date OF
Time to Next Treatment
measured 1 Year
Time to Discontinuation
measured 1 Year
Overall survival (OS)
measured 1 Year
real-world Progression free survival (rwPFS)
measured 1 Year

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