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A Study to Learn About the Vepdegestrant (ARV-471, PF-07850327) in People With ER+/HER2- Locally Advanced or Metastatic Breast Cancer (BC)

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NCT05463952 · results posted

Sponsored by Pfizer (industry) · PFE — their whole pipeline →. With Arvinas Estrogen Receptor, Inc..

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
6actual
Sites
3
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
DateFiledBasisWhat it is
Start2022-08-16actualWhen the study began enrolling
Primary completion2023-05-04actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-03-31estimatedThe whole study's end, after follow-up
First posted2022-07-19actualWhen this record first appeared on the registry
Results posted2024-09-23actualWhen the sponsor posted results to the registry
Record updated2024-11-13actualThe 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: vepdegestrant — also filed as ARV-471, PF-07850327

Primary outcome

what the primary-completion date above is the date OF
Number of Participants With Dose Limiting Toxicity (DLTs) During First Treatment Cycle
measured Cycle 1 (28 days)

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2022-10-21 · 1.8 MB · Prot_000.pdf
Statistical Analysis Planposted 2023-05-25 · 504 KB · SAP_001.pdf

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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