A Real-life Study to Understand the Use and Effects of Palbociclib in US Patients With Breast Cancer
Running, not enrolling
Conditions studied: Breast Cancer, Malignant Neoplasm of Breast
In brief
Palbociclib, the first oral CDK4/6 inhibitor, is an approved medicine indicated for the treatment of a kind of advanced/metastatic breast cancer (MBC), called hormone receptors positive (HR+)/ Human epidermal growth factor receptor 2 negative (HER2-) disease. Palbociclib is given orally in combination with hormonal therapies. The purpose of this study is to better understand how Palbociclib combination is used in real-life conditions and its clinical impact compared with hormonal therapy. The study will also evaluate how long patients take the different CDK 4/6 inhibitor drugs and whether using those drugs impacts the use of chemotherapy later. Male and female patients aged 18 years old or more presenting the following conditions will be selected for the study: * HR+/HER2- MBC * First treatment with Palbociclib, hormonal therapy, or other CDK4/6 inhibitors after MBC diagnosis The study will use data without personal identity, which were obtained from medical records in routine clinical practice.
Key facts
- Study ID
- NCT06495164
- Run by
- Pfizer
- People needed
- 1
- Starts
- 2024-06-24
- Expected to finish
- 2026-12-30
- Last updated by the study team
- 2025-11-25
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Pfizer New York — New York, New York, United States
Full record on ClinicalTrials.gov
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