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PROVIDENCE - Prospective Non-interventional Study (NIS) to Examine Patient-reported Outcomes and Real-world Clinical Data in Patients With HER2-positive, HER2-low or HER2-ultralow Unresectable or Metastatic Breast Cancer Treated With Trastuzumab Deruxtecan

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NCT05573893 · readout in 1,960 d

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →. With Daiichi Sankyo.

Phase
Status
Recruiting
Study type
Observational
Enrollment
800estimated
Sites
109
Country
Germany

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
Start2023-09-12actualWhen the study began enrolling
Primary completion2031-12-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2031-12-31estimatedThe whole study's end, after follow-up
First posted2022-10-10actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Breast Neoplasms
  • Breast Cancer
  • Neoplasm Metastasis

Primary outcome

what the primary-completion date above is the date OF
Real-world Time To Next Treatment (rwTTNT1)
measured From first dose of T-DXd until initiation of subsequent therapy or death of any cause, whichever came first, assessed up to 60 months

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