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BGB-43395 Plus Letrozole Versus CDK4/6i Plus Letrozole for Patients With Advanced or Metastatic HR+/HER2- Breast Cancer Who Have Not Received Prior Treatment for Advanced or Metastatic Disease

RecruitingPhase 3

An Open-Label, Randomized, Multicenter Phase 3 Study Investigating the Efficacy and Safety of BGB-43395 Plus Letrozole Versus CDK4/6 Inhibitors (Abemaciclib, Palbociclib, Ribociclib) Plus Letrozole in Patients With Advanced or Metastatic HR+/HER2- Breast Cancer Who Have Not Received Prior Systemic Anticancer Treatment for Advanced or Metastatic Disease

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Participants must be at least 18 years of age or the legal age of consent in the jurisdiction in which the study is taking place at the time of signing the informed consent.
* Participants with histologically confirmed locally advanced or metastatic HR+ HER2- breast cancer.
* Participants must have a stable Eastern Cooperative Oncology Group (ECOG) Performance Status of ≤ 1.
* Adequate organ function.

Exclusion Criteria:

* Participants who have received prior systemic treatment in the advanced or metastatic setting.
* Participants who have received prior treatment with any selective cyclin-dependent kinase 4 (CDK4) or cyclin-dependent kinase 2 (CDK2) targeting agent, or any other investigational anticancer drug in any disease setting, except for prior investigational or approved SERDs in the adjuvant setting, provided that disease recurrence occurred more than 12 months after the last dose of endocrine-based therapy.
* Participants with active leptomeningeal disease or uncontrolled, untreated brain metastasis.

Note: Other protocol-defined inclusion/exclusion criteria may apply.

About the study

The purpose of this study is to investigate the efficacy and safety of BGB-43395 in combination with letrozole compared with investigator's choice of cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) in combination with letrozole in patients with advanced or metastatic hormone receptor positive (HR+)/human epidermal growth factor receptor 2 negative (HER2-) breast cancer (BC) who have not received prior systemic treatment for advanced or metastatic disease.

What is being tested

Sponsor: BeOne Medicines · Participants: 1,056 · Started: May 22, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07492641

Locations in the U.S.

AlabamaAlabama Oncology Princeton, Birmingham
AlaskaAlaska Oncology and Hematology, Llc, Anchorage
Fairbanks Cancer Care Physicians Pc, Fairbanks
ArizonaPioneer Research Center, Bullhead City
Ironwood Cancer and Research Centers Chandler Ii, Chandler
ArkansasGenesis Cancer and Blood Institute Hot Springs (Harmony Park), Hot Springs
CaliforniaHelios Clinical Research the Oncology Institute Fountain Valley, Fountain Valley
California Research Institute, Los Angeles
Ventura County Hematology Oncology Specialists, Oxnard
FloridaBrcr Coral Springs, Coral Springs
Mid Florida Hematology and Oncology Center, Orange City
Cancer Care Centers of Brevard Palm Bay, Palm Bay
Florida Clinical Trials Group Plantation, Plantation
Hematology Oncology Associates of the Treasure Coast, Port Saint Lucie
The Oncology Institute of Hope and Innovation South Miami, South Miami
Florida Clinical Trials Group Tamarac, Tamarac
Moffitt Cancer Center McKinley Campus Richard M Shulze Family Foundation Outpatient Center, Tampa
GeorgiaUniversity Cancer and Blood Center Athens Comprehensive Cancer Center, Athens
Central Georgia Cancer Care Macon Office, Macon
HawaiiHawaii Cancer Care, Honolulu
IllinoisHope and Healing Cancer Services, Hinsdale
Cancer Care Specialists For Illinois, OFallon
IndianaFort Wayne Medical Oncology and Hematology, Fort Wayne
Hematology Oncology of Indiana, Indianapolis
IowaMercy Medical Center, Cedar Rapids
KentuckyOwensboro Health Mitchell Memorial Cancer Center, Owensboro
MichiganKarmanos Cancer Institute, Detroit
MinnesotaAspirus St Lukes Hospital, Duluth
Metro Minnesota Community Oncology Research Consortium (Mmcorc), Saint Paul
MissouriOncology Hematology Associates, Springfield
NebraskaNebraska Cancer Specialists St Francis Grand Island, Grand Island
Cancer Partners of Nebraska April Sampson Cancer Center, Lincoln
Nebraska Cancer Specialists, Omaha
NevadaComprehensive Cancer Centers of Nevada, Las Vegas
Renown Regional Medical Center, Reno
New JerseyAstera Cancer Care East Brunswick, East Brunswick
Summit Medical Group, Florham Park
Rutgers Cancer Institute of New Jersey, New Brunswick
New YorkNyu Langone Health Perlmutter Cancer Center Sunset Park, Brooklyn
Nyu Langone Health Perlmutter Cancer Center At Nyu Langone Hospital Long Island, Mineola
Nyu Langone Health Perlmutter Cancer Center 34Th Street, New York
University of Rochester, Rochester
New York Cancer and Blood Specialists, Shirley
North CarolinaPardee Cancer Center, Hendersonville
Carolina Cancer Research Center, Wilson
OhioGabrail Cancer Center Research, Canton
Dayton Physicians Network, Dayton
OregonOncology Associates of Oregon Willamette Valley Cancer Center, Eugene
Oregon Oncology Specialists, Salem
PennsylvaniaConsultants in Medical Oncology and Hematology Cancer Center At Broomall, Broomall
McGlinn Cancer Institute, West Reading
TennesseeBallad Health Cancer Center Kingsport, Kingsport
TexasTexas Oncology Austin Central, Austin
UtahUtah Cancer Specialists Cancer Center, Salt Lake City
VirginiaOncology and Hematology Associates of Southwest Virginia, Inc (Us Oncology Research), Blacksburg
Virginia Cancer Specialists, Fairfax
Virginia Cancer Institute, Richmond
WashingtonVista Oncology East Olympia, Olympia
Multicare Cancer Institute Deaconess Medical Office Building 1, Spokane
Multicare Cancer Institute Tacoma General Hospital, Tacoma
Northwest Medical Specialties, Tacoma
Multicare Cancer Institute North Star Lodge, Yakima
WisconsinGundersen Health System, La Crosse

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.