For Healthcare Professionals

A Study Of Palbociclib (PD-0332991) + Letrozole VS. Placebo+ Letrozole For 1st Line Treatment Of Asian Postmenopausal Women With ER+/HER2- Advanced Breast Cancer [PALOMA-4]

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About the study

The study is designed to compare the clinical benefit following treatment with letrozole in combination with Palbociclib versus letrozole in combination with placebo in Asian postmenopausal women with ER(+)/HER2(-) advanced breast cancer who have not received prior systemic anti cancer therapies for their advanced/metastatic disease.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Adult Asian women with locoregionally recurrent or metastatic disease not amenable to curative therapy
  2. Confirmed diagnosis of ER positive breast cancer
  3. No prior systemic anti-cancer therapy for advanced ER+ disease
  4. Postmenopausal women
  5. Measurable disease as per Response Evaluation Criterion in Solid Tumors [RECIST] or bone-only disease
  6. Eastern Cooperative Oncology Group [ECOG] 0-1
  7. Adequate organ and marrow function
  8. Patient must agree to provide tumor tissue

EXCLUSION CRITERIA

Exclusion Criteria:


  1. Confirmed diagnosis of HER2 positive disease
  2. Patients with advanced, symptomatic, visceral spread that are at risk of life threatening complication in the short term
  3. Known uncontrolled or symptomatic CNS metastases
  4. Prior neoadjuvant or adjuvant treatment with a non steroidal aromatase inhibitor (ie, anastrozole or letrozole) with disease recurrence while on or within 12 months of completing treatment
  5. Prior treatment with any CDK 4/6 inhibitor

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

Breast Neoplasms

Age (in years)

18 - 70

Phase

Phase 3

Participants needed

340

Est. Completion Date

Dec 31, 2024

Treatment type

Interventional


Sponsor

Pfizer

ClinicalTrials.gov identifier

NCT02297438

Study number

A5481027

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