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NCT06003114Completed

A Study to Understand the Use of Palbociclib in Canadian Patients With Breast Cancer That Has Spread to Other Organs

Real-World Utilization of Palbociclib as 1L Treatment in Canadian HR+/HER2-women Breast Cancer Patients

Source: ClinicalTrials.gov · Last updated 10 Jul 2026

Brief summary (registry, in English)

The purpose of this real-world study is to understand the use of palbociclib as first treatment for Hormone receptor positive (HR+) and Human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer in Canada (PALCAN). The real-world study is not a research study. It involves real patients who receive medicines prescribed by their doctors in the real world. Metastatic breast cancer is the type which has spread from breast to other organs. HR positive stands for Hormone-receptor cells that have a protein on their surface that binds to one of 2 types of hormones. They are estrogen or progesterone. Both these hormones help cancer cells grow. HER2 negative describes cells that have a small amount or none of a protein called HER2 on their surface. In normal cells, HER2 helps control cell growth. Cancer cells that are HER2 negative may grow more slowly and are less likely to come back or spread to other parts of the body. This study will mainly measure: \- duration of treatment (from start of treatment till end of treatment) among a group of patients taking palbociclib (Ibrance) in combination with hormone therapy as first line treatment for HR+ HER2- metastatic breast cancer.

Status (registry)
Completed
Study type
Observational
Enrollment
472 (actual)
First submitted
10 Aug 2023
Start date
Oct 2023
Primary completion date
Feb 2024
Lead sponsor
Pfizer
NCT number
NCT06003114

What you commit to

  • Study type: Observational
  • Participants enrolled: 472
  • From Oct 2023 to the primary completion date, Feb 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Received a different CDK4/6 inhibitor before palbociclib in the first line
  • Received other systemic therapy, including hormone therapy, 15-60 days prior to initiation of palbociclib
  • Invalid or incomplete records (more specifically, complete duration of treatment on palbociclib, endocrine therapy or LHRH)

Other

  • Death date recorded on or before the date of index date

Who the study is looking for

  • Received at least one cycle of palbociclib as first line therapy for metastatic breast cancer between 01 January 2016 and 31 December 2022
  • Histologically confirmed HR+/HER2- metastatic breast cancer
  • Minimum of 3 months available follow-up on palbociclib

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Alberta Health Services
Coordinator of this site? Confirm its status
EdmontonCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.