Ireland
--:--IST
Active, not recruiting Phase 3

Phase IIIb Study of Ribociclib + ET in Early Breast Cancer

NCT05827081 · tracked via the Priya Life Science USA tracker
Phase
Phase 3
Started
2024-02-28
Last updated
2026-10-23

Condition(s) studied

Early Breast Cancer

Investigational drug(s) / intervention(s)

Ribociclib →Letrozole →AnsastrozoleGoserelin →Leuprolide →Exemestane →

Ribociclib: Ribociclib 400 mg orally once daily on days 1-21 of a 28 day cycle followed by 7 days rest

Letrozole: Letrozole 2.5 mg orally once daily continuously

Ansastrozole: Anastrozole 1 mg orally once daily continuously.

Goserelin: Goserelin administered subcutaneously at 3.6 mg once every 4 weeks if the one-month depot formulation is used or at 10.8 mg once every 3 months if the three-month depot formulation is used

Leuprolide: Leuprolide administered subcutaneously at 3.75 mg once every 4 weeks if the one-month depot formulation is used or at 11.25 mg once every 3 months if the three-month depot formulation is used

Exemestane: Exemestane 25 mg once daily continuously

Study summary

The purpose of this open-label, multicenter, phase IIIb, single-arm study is to characterize the efficacy and safety of the combination of ribociclib and standard adjuvant endocrine therapy (ET) on invasive breast cancer-free survival (iBCFS), in a close to clinical practice patient population with HR-positive (HR+), HER2-negative (HER2-), Anatomic Stage Group III, IIB, and a subset of Stage IIA Early Breast Cancer (EBC).

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Key Inclusion criteria: * Participant is an adult, male or female ≥ 18 years of age at the time of informed consent form signature (IC). * Participant has a histologically and/or cytologically confirmed diagnosis of estrogen-receptor positive and/or progesterone receptor positive breast cancer (BC) based on the most recently analyzed tissue sample tested by a local laboratory prior to enrollment. * Participant has HER2- BC defined as a negative in situ hybridization test or an immunohistochemistry (IHC) status of 0, 1+ or 2+. If IHC is 2+, a negative in situ hybridization (FISH, CISH, or SISH) test is required by local laboratory testing based on the most recently analyzed tissue sample. * Participants may have already received any standard neoadjuvant and/or adjuvant ET, including tamoxifen or toremifene at the time of informed consent signature, but enrollment should occur within 36 months of prior ET start date and participants should have at least 3 years remaining of endocrine adjuvant therapy. * For participants with prior ET treatment \> 12 months, restaging is highly recommended (unless contradictory to local regulations) to rule out disease recurrence prior to enrollment. * The number of participants with prior ET between 12 and 36 months will be capped at 30%. The cap will not apply to Black or African American participants. * Participant has no contraindication to receive adjuvant ET in the study. * Participant after surgical resection where tumor was removed completely, with the final surgical specimen microscopic margins free from tumor, and belongs to one of the following categories: * Anatomic Stage Group III, or * Anatomic Stage Group IIB, or * A subset of Anatomic Stage Group IIA. * Participant has an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1 or 2. * Participant has adequate bone marrow and organ function. * ECG values assessed by KardiaMobile-6L device, or standard 12-lead ECG per local investigator where KardiaMobile-6L cannot be used, as: * QTcF interval at Screening \< 450 msec (QT interval using Fridericia's correction). * Mean resting heart rate 50-99 beats per minute (determined from the ECG). Key Exclusion criteria: * Participant with distant metastases of BC beyond regional lymph nodes (Stage IV according to AJCC 8th edition) and/or evidence of recurrence after curative surgery. * Participant is concurrently using other antineoplastic therapy with the exception of adjuvant ET. * Participant has any other concurrent severe and/or uncontrolled medical condition that would, in the Investigator's judgment, cause unacceptable safety risks, contraindicate participant participation in the clinical study or compromise compliance with the protocol, or limit life expectancy to ≤5 years. * Clinically significant, uncontrolled heart disease and/or cardiac repolarization abnormality. * Pregnant or breast-feeding (lactating) women or women who plan to become pregnant or breast-feed during the trial. * Women of child-bearing potential (CBP), defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception while taking study treatment and for 21 days after stopping the treatment. Other inclusion/exclusion criteria may apply

Primary outcome measure(s)

  • Invasive Breast Cancer Free Survival (iBCFS) rate at 3 years — At 3 years
    iBCFS is defined as the time from the date of first dose to the date of the first event of invasive ipsilateral breast tumor recurrence, local/regional invasive recurrence, distant recurrence, death (any cause), or contralateral invasive BC. iBCFS will be assessed using STEEP criteria version 2.0 (Standardized Definitions for Efficacy End Points in Adjuvant Breast Cancer Trials), as assessed by Investigator. The iBCFS rate at 3 years will be assessed.

Trial sites (214)

FacilityCityRegionStatus
Central Alabama Research Birmingham Alabama
Alaska Oncology and Hematology LLC Anchorage Alaska
Western Reg MC-COH Phoenix Goodyear Arizona
CARTI Cancer Center Little Rock Arkansas
Beverly Hills Cancer Center Beverly Hills California
Onco Inst of Hope and Innovation Cerritos California
City of Hope National Medical Duarte California
Providence Medical Foundation Fullerton California
Los Angeles Cancer Network Good Samaritan Los Angeles California
El Camino Hospital Mountain View California
Palo Alto Medical Foundation Mountain View California
UC Irvine Medical Center Orange California
Sutter Inst Medical Research Sacramento California
School Of Medicine Sacramento California
Sharp Rees Stealy Medical Group Inc San Diego California
Rocky Mountain Cancer Centers Denver Colorado
Georgetown University Lombardi Cancer Center Washington D.C. District of Columbia
Medstar Washington Hospital Center Washington D.C. District of Columbia
AdventHealth Altamonte Springs Altamonte Springs Florida
Holy Cross Health Fort Lauderdale Florida
Hialeah Hospital Hialeah Florida
Memorial Cancer Institute Hollywood Florida
Jupiter Medical Center Jupiter Florida
Ocala Research Institute Inc Ocala Florida
Summit Cancer Care PC Savannah Georgia
Affiliated Oncologists IL Chicago Illinois
Hope And Healing Care Hinsdale Illinois
Midwestern Reg MC COH Chicago Zion Illinois
Investigative Clinical R of Indiana Indianapolis Indiana
University of Iowa Health Care Waukee Iowa
University of Kansas Cancer Center Westwood Kansas
Cancer Center of Kansas Wichita Kansas
Willis-Knighton Cancer Center Shreveport Louisiana
Mercy Medical Center Baltimore Maryland
Maryland Oncology Hematology P A Silver Spring Maryland
Boston Medical Center Boston Massachusetts
Dana Farber Cancer Institute Boston Massachusetts
Minnesota Oncology Hematology P A Minneapolis Minnesota
Allina Hlth Cancer Inst Minneapolis Minneapolis Minnesota
Jackson Oncology Associates Jackson Mississippi

+ 174 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05827081 on ClinicalTrials.gov ↗ ← All trials in the USA