A Study to Learn About the Study Medicine Called PF-07220060 in Combination With Fulvestrant in People With HR-positive, HER2-negative Advanced or Metastatic Breast Cancer Who Progressed After a Prior Line of Treatment

Running, not enrolling · Phase 2

Conditions studied: Advanced or Metastatic Breast Cancer

In brief

The purpose of this study is to learn about the safety and how effective the study medicine (PF-07220060) plus fulvestrant is compared to the study doctor's choice of treatment in people with advanced or metastatic breast cancer. Advanced cancer is the one that is unlikely to be cured or taken care of with treatment. Metastatic cancer is the one that has spread to other parts of the body. This study is seeking female and male participants who: * are 18 years of age or older; * are hormone receptor (HR)-positive and human epidermal growth factor receptor 2 (HER2)-negative; * have advanced or metastatic breast cancer after taking other treatments before this study; * have not taken or need to take medications that are not allowed by the study protocol; * do not have any medical or mental conditions that may increase the risk of study participation. Half of the participants will take PF-07220060 two times daily by mouth along with fulvestrant. Fulvestrant will be given as a shot into the muscle. The other half will take the study doctor's choice of treatment which can either be: * Fulvestrant alone taken as shot into the muscle. * Everolimus along with exemestane taken once daily by mouth. This study will compare the experiences of participants receiving the study medicine plus fulvestrant to those who are receiving the study doctor's choice of treatment. This will help decide if the study medicine is safe and effective. Participants will receive study treatment and/or will be in the study until: * imaging scans (such as an MRI and/or CT) show that their cancer is getting worse. * the study doctor thinks the participant is no longer benefitting from the study medicine. * has side effects that become too severe. A side effect is a reaction (expected or unexpected) to a medicine or treatment you take. * the participant chooses to stop taking part.

Key facts

Study ID: NCT06105632
Run by: Pfizer
People needed: 333
Starts: 2024-01-09
Expected to finish: 2028-01-21
Last updated by the study team: 2026-02-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Histological confirmation of breast cancer with evidence of locally advanced or metastatic disease, which is not amenable to surgical resection or radiation therapy with curative intent.
Documented estrogen receptor (ER) and/or progesterone receptor (PR)- positive tumor
Documented HER2-negative tumor
Able to provide a sufficient amount of representative formalin fixed, paraffin embedded (FFPE) tumor tissue specimen.
Must have received CDK4/6i plus NSAI defined per study protocol. There must be documented PD during or after CDK4/6i treatment.
Measurable disease or non-measurable bone only disease as defined by RECIST version 1.1.
Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) ≤2.

You may not qualify if…

Any medical or psychiatric condition that may increase the risk of study participation or make the participant inappropriate for the study.
In visceral crisis at risk of immediately life-threatening complications in the short term.
Known active uncontrolled or symptomatic central nervous system metastases, carcinomatous meningitis, or leptomeningeal disease.
Prior treatment with any of the following:
Everolimus or investigational anti-cancer agents in any setting
Prior chemotherapy in the advanced setting
Radiation within 2 weeks of randomization
Current use or anticipated need for any prohibited food, supplements or concomitant medication(s) (ie, other anti-cancer therapies, other endocrine therapies, growth factors, chronic systemic corticosteroids, strong cytochrome P450 3A4/5 [CYP3A4/5] or uridine 5' diphosphate-glucuronosyltransferase 2B7 [UGT2B7] inhibitors and inducers, direct oral anticoagulants, proton pump inhibitors).
Inadequate renal function, hepatic dysfunction, or hematologic abnormalities.

Where it is running

Harbin Medical University Cancer Hospital — Harbin, Heilongjiang, China
Henan Cancer Hospital — Zhengzhou, Henan, China
Hoag Health Center Irvine — Irvine, California, United States
Hoag Hospital Irvine — Irvine, California, United States
Keck Hospital of USC — Los Angeles, California, United States
Los Angeles General Medical Center — Los Angeles, California, United States
USC/Norris Comprehensive Cancer Center — Los Angeles, California, United States
Hoag Memorial Hospital Presbyterian — Newport Beach, California, United States
Keck Medical Center of USC Pasadena — Pasadena, California, United States
Danbury Hospital — Danbury, Connecticut, United States
Norwalk Hospital — Norwalk, Connecticut, United States
Georgetown University Medical Center — Washington D.C., District of Columbia, United States
MedStar Washington Hospital Center — Washington D.C., District of Columbia, United States
Intermountain Health St. Vincent Regional Hospital — Billings, Montana, United States
Intermountain Health St. Vincent Regional Hospital - Cancer Centers of Montana — Billings, Montana, United States
Cancer Care Specialists — Reno, Nevada, United States
Vassar Brothers Medical Center — Poughkeepsie, New York, United States
Memorial Hermann Cancer Center — Houston, Texas, United States
Baylor Scott & White Medical Center - Round Rock — Round Rock, Texas, United States
Centro de Investigaciones Medicas y Desarrollo LC — Buenos Aires, Buenos Aires F.D., Argentina
CIPREC — Buenos Aires, Buenos Aires F.D., Argentina
Organizacion Medica de Investigacion — CABA, Buenos Aires F.D., Argentina
Clinica Viedma S. A — Viedma, Río Negro Province, Argentina
Instituto de Oncología de Rosario — Rosario, Santa Fe Province, Argentina
Guangxi Medical University Affiliated Tumor Hospital — Nanning, Guangxi, China

Full record on ClinicalTrials.gov

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