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Study for Participants Continuing From Pfizer-sponsored Palbociclib (a Study Medicine) Studies

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NCT05226871 · readout in 134 d

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

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
35actual
Sites
23
Countries
China, Mexico, South Korea +4

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
Start2022-07-07actualWhen the study began enrolling
Primary completion2026-12-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-12-31estimatedThe whole study's end, after follow-up
First posted2022-02-07actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-11-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Breast Cancer
  • Head and Neck Cancer

Interventions

  • Drug: Palbociclib — also filed as IBRANCE
  • Drug: Cetuximab
  • Drug: Fulvestrant
  • Drug: Letrozole

Primary outcome

what the primary-completion date above is the date OF
Number/Percentage of Participants with Treatment-Emergent Adverse Events (AEs) Leading to Permanent Discontinuation of Study Treatment and Serious Adverse Events (SAEs)
measured Baseline up to 28 days after last dose of study intervention

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