Ibrance

Drug

Drug Profile

Ibrance is the brand name of palbociclib, a cyclin-dependent kinase 4/6 (CDK4/6) inhibitor for hormone receptor-positive, HER2-negative advanced or metastatic breast cancer. It is used in combination endocrine regimens such as aromatase inhibitors or fulvestrant. The FDA first approved Ibrance on February 3, 2015.

Drug Class
Cyclin-dependent kinase 4/6 (CDK4/6) inhibitor
Approval Status
FDA approved; first approved February 3, 2015.
Mechanism of Action
Cyclin-dependent kinase 4/6 (CDK4/6) inhibition.
Brand Names
  • Ibrance
Indications
  • \HR-positive, HER2-negative advanced or metastatic breast cancer (with aromatase inhibitor or fulvestrant)\

Related News

Phase 3 Breast Cancer Trial Data Highlights from Q1 2026

Multiple phase 3 breast cancer trials reported significant findings in early 2026, including positive results for novel therapies across different subtypes. Key data includes progression-free survival benefits for palbociclib in HR-positive, HER2-positive advanced breast cancer and investigations of antibody-drug conjugates and combination therapies. Full trial findings are expected to be presented at upcoming medical meetings.

Related Clinical Trials

NCT ID Title Status Phase
NCT06962969

A Study to Understand the Patients Confirmed to Have Advanced or Metastatic Breast Cancer and Receiving Palbociclib Treatment Using a Real-world Database

COMPLETED
NCT04874025

Observational Analysis of Palbociclib Treatment in Patients With First Line Therapy for Locally Advanced and/or Metastatic Breast Cancer

COMPLETED
NCT02059213

A Phase II Study of Androgen Deprivation Therapy With or Without Palbociclib in RB-Positive Metastatic Prostate Cancer

COMPLETED PHASE2