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ABCSG 63 / ERIKA: Elacestrant and RIbociclib in Ki67-tested endocrine responsive breAst cancer: An open-label, two-arm, randomized, phase II study of elacestrant plus ribociclib vs. AI (plus GnRH agonist in pre-/perimenopausal women and men) plus ribociclib as neoadjuvant therapy for endocrine-responsive HER2-negative early breast cancer
EU CTIS ID: 2023-505758-17-00
What this study is testing
To evaluate the superiority of elacestrant plus ribociclib vs. AI (and GnRH agonist in pre-/perimenopausal women and men) plus ribociclib in endocrine-responsive early breast cancer, when measured by modified PEPI score at the time of surgery
- Therapeutic exploratory (Phase II)
A plain-language read of the study's public EU CTIS listing. The study team confirms the details.
Who can take part
You may be able to join if
- (1) Signed informed consent obtained prior to any study specific assessments and procedures which are not performed as part of standard of care
- (10) Serum potassium ≥3mmol/L, serum sodium ≥130mmol/L, serum calcium ≤2.9mmol/L, serum albumin ≥3.0 g/dL (≥30 g/L), serum phosphate ≥2.5mg/dL and serum magnesium ≥0.5mmol/L (intake of (multi)vitamin supplements allowed)
- (11) Aspartate amino transferase (AST), alanine amino transferase (ALT), and alkaline phosphatase (ALP) < 3 x ULN
- (12) Total serum bilirubin ≤1.5 x ULN with the following exception: Patients with known Gilbert’s syndrome: total serum bilirubin level ≤ 3.0 x ULN or direct bilirubin ≤1.5 x ULN
- (13) Serum creatinine ≤ 1.5 x ULN or creatinine clearance ≥ 50 mL/min (calculated using the Cockcroft-Gault formula); - - Creatinine clearance (male) = ([140-age in years] × weight in kg)/ ([serum creatinine in mg/dL] × 72); - - Creatinine clearance (female) = (0.85 × [140-age in years] × weight in kg)/ ([serum creatinine in mg/dL] × 72)
- (14) Patients must have a 12-lead ECG with all of the following parameters at screening: - QTcF interval (using Fridericia’s correction) < 450 ms; - Resting heart rate ≥ 50 bpm
You likely can't join if
- (1) Metastatic or locally advanced disease (without loco-regional treatment options with curative intention) as per local standard
- (10) Serious medical or psychiatric disorders that would, in the investigator’s judgement, interfere with the patient’s safety or informed consent (e.g., known chronic pancreatitis, known chronic active hepatitis, known active untreated or uncontrolled fungal, bacterial or viral infections; - Patients with known HBV and/or HCV infection (testing only required, if clinically indicated) must have undetectable viral load during screeningns, etc.); - Patients known to be HIV+ (testing only required, if clinically indicated) are allowed if they have undetectable viral load at screening
- (11) Clinically significant, uncontrolled heart disease and/or cardiac repolarization abnormalities, including but not limited to any of the following: - History of acute coronary syndromes (including myocardial infarction, unstable angina, coronary artery bypass grafting, coronary angioplasty, or stenting) or symptomatic pericarditis within 6 months prior to screening; - - History of documented congestive heart failure (New York Heart Association functional classification III-IV); - Documented cardiomyopathy; - - Clinically significant cardiac arrhythmias (e.g., ventricular tachycardia), complete left bundle branch block, high-grade AV block (e.g., bifascicular block, Mobitz type II and third-degree AV block); - - Long QT syndrome or family history of idiopathic sudden death or congenital long QT syndrome, or any of the following: - i. Risk factors for Torsades de Pointe (TdP) including uncorrected hypokalemia or hypomagnesemia, history of cardiac failure, or history of clinically significant/symptomatic bradycardia; - ii. Inability to determine the QTcF interval (Fridericia’s correction) during screening; - Systolic blood pressure (SBP) >160 mmHg or <90 mmHg at screening
- (12) Documented pneumonitis/ILD prior to randomization
- (13) Patient is currently receiving or has received any of the following medications that cannot be discontinued within 14 days or 5 half-lives, whichever is shorter, prior to first dose of the study: - Herbal preparations/medications known as strong inducers or inhibitors of CYP3A4 or those with a known risk of QT prolongation. These include, but are not limited to, St. John’s wort, kava, ephedra (ma huang), gingko biloba, DHEA, yohimbe, saw palmetto, and ginseng; - Medications, and/or foods including fruits (e.g., grapefruit, pumeloes, star fruit, Seville oranges) and their juices that are known strong and moderate inducers or inhibitors of CYP3A4; - Medications with a known risk to prolong the QT interval and/or known to cause Torsades de Pointe that cannot be discontinued or replaced by safe alternative medication 14 days prior to randomization; - Medications that have a narrow therapeutic index and are predominantly metabolized through CYP3A4/5; - Systemic corticosteroids
- (14) Patients receiving live, attenuated vaccine within 7 days prior to randomization AND not fit for study participation as per investigator’s assessment
See the full eligibility criteria
Who can join
- (1) Signed informed consent obtained prior to any study specific assessments and procedures which are not performed as part of standard of care
- (10) Serum potassium ≥3mmol/L, serum sodium ≥130mmol/L, serum calcium ≤2.9mmol/L, serum albumin ≥3.0 g/dL (≥30 g/L), serum phosphate ≥2.5mg/dL and serum magnesium ≥0.5mmol/L (intake of (multi)vitamin supplements allowed)
- (11) Aspartate amino transferase (AST), alanine amino transferase (ALT), and alkaline phosphatase (ALP) < 3 x ULN
- (12) Total serum bilirubin ≤1.5 x ULN with the following exception: Patients with known Gilbert’s syndrome: total serum bilirubin level ≤ 3.0 x ULN or direct bilirubin ≤1.5 x ULN
- (13) Serum creatinine ≤ 1.5 x ULN or creatinine clearance ≥ 50 mL/min (calculated using the Cockcroft-Gault formula); - - Creatinine clearance (male) = ([140-age in years] × weight in kg)/ ([serum creatinine in mg/dL] × 72); - - Creatinine clearance (female) = (0.85 × [140-age in years] × weight in kg)/ ([serum creatinine in mg/dL] × 72)
- (14) Patients must have a 12-lead ECG with all of the following parameters at screening: - QTcF interval (using Fridericia’s correction) < 450 ms; - Resting heart rate ≥ 50 bpm
- (15) Willingness and ability to provide FFPE tumor tissues and liquid biopsies for mandatory translational research program
- (2) Women or men, age ≥ 18 years at the time of initially signing the study specific informed consent form(s) (ICF). Female patients may be either postmenopausal, premenopausal or perimenopausal. Refer to section 11.2, for definitions on the menopausal status.
- (3) Histologically confirmed invasive, (unilateral or bilateral) adenocarcinoma of the breast with the following characteristics: - cT1c-4a-c, cN0-3, M0 per AJCC (American Joint Committee on Cancer) Breast Cancer Staging version 8 (refer to section 23.3); - In case of a multifocal tumor (defined as the presence of two or more foci of cancer within the same breast quadrant) or multicentric tumor (defined as the presence of two or more foci of cancer within different quadrants), the overall largest lesion must be > 1 cm and designated as the “target” lesion for all subsequent tumor evaluations; - Histologically confirmed HER2-negative tumors; HER2 measurement to be assessed locally according to the ASCO/CAP guideline; - ER-positive tumors (i.e. > 10 % positive stained tumor cells); - PR-positive or negative tumors
- (4) ECOG performance status 0-1
- (5) In women of childbearing potential, urine or serum pregnancy test must be negative within 28 days prior to randomization. In postmenopausal women or hysterectomized patients, pregnancy tests do not need to be performed. - Women of childbearing potential and men must use adequate contraception that results in a failure rate <1 % per year during the study treatment. In case of women of childbearing potential, until 180 days after the last dose of study treatment and in case of men with female partners of childbearing potential, until 120 days after the last dose of study treatment; - - Men or women must abstain from donating sperm or ova during the study treatment. In case of women, until 180 days after the last dose of study treatment and in case of men, until 120 days after the last dose of study treatment
- (6) Absolute neutrophile count (ANC) ≥ 1.5 x 109/L (1500/µL) without granulocyte colony-stimulating factor (G-CSF) support
- (7) Platelet count ≥ 100 x 109/L (100,000/µL) without transfusion
- (8) Hemoglobin ≥ 90 g/L (9 g/dL). Patients may be transfused only once to meet this criterion
- (9) For patients not receiving therapeutic anticoagulation: INR or aPTT ≤ 1.5 x ULN. For patients receiving therapeutic anticoagulation: stable anticoagulant regimen
What rules you out
- (1) Metastatic or locally advanced disease (without loco-regional treatment options with curative intention) as per local standard
- (10) Serious medical or psychiatric disorders that would, in the investigator’s judgement, interfere with the patient’s safety or informed consent (e.g., known chronic pancreatitis, known chronic active hepatitis, known active untreated or uncontrolled fungal, bacterial or viral infections; - Patients with known HBV and/or HCV infection (testing only required, if clinically indicated) must have undetectable viral load during screeningns, etc.); - Patients known to be HIV+ (testing only required, if clinically indicated) are allowed if they have undetectable viral load at screening
- (11) Clinically significant, uncontrolled heart disease and/or cardiac repolarization abnormalities, including but not limited to any of the following: - History of acute coronary syndromes (including myocardial infarction, unstable angina, coronary artery bypass grafting, coronary angioplasty, or stenting) or symptomatic pericarditis within 6 months prior to screening; - - History of documented congestive heart failure (New York Heart Association functional classification III-IV); - Documented cardiomyopathy; - - Clinically significant cardiac arrhythmias (e.g., ventricular tachycardia), complete left bundle branch block, high-grade AV block (e.g., bifascicular block, Mobitz type II and third-degree AV block); - - Long QT syndrome or family history of idiopathic sudden death or congenital long QT syndrome, or any of the following: - i. Risk factors for Torsades de Pointe (TdP) including uncorrected hypokalemia or hypomagnesemia, history of cardiac failure, or history of clinically significant/symptomatic bradycardia; - ii. Inability to determine the QTcF interval (Fridericia’s correction) during screening; - Systolic blood pressure (SBP) >160 mmHg or <90 mmHg at screening
- (12) Documented pneumonitis/ILD prior to randomization
- (13) Patient is currently receiving or has received any of the following medications that cannot be discontinued within 14 days or 5 half-lives, whichever is shorter, prior to first dose of the study: - Herbal preparations/medications known as strong inducers or inhibitors of CYP3A4 or those with a known risk of QT prolongation. These include, but are not limited to, St. John’s wort, kava, ephedra (ma huang), gingko biloba, DHEA, yohimbe, saw palmetto, and ginseng; - Medications, and/or foods including fruits (e.g., grapefruit, pumeloes, star fruit, Seville oranges) and their juices that are known strong and moderate inducers or inhibitors of CYP3A4; - Medications with a known risk to prolong the QT interval and/or known to cause Torsades de Pointe that cannot be discontinued or replaced by safe alternative medication 14 days prior to randomization; - Medications that have a narrow therapeutic index and are predominantly metabolized through CYP3A4/5; - Systemic corticosteroids
- (14) Patients receiving live, attenuated vaccine within 7 days prior to randomization AND not fit for study participation as per investigator’s assessment
- (15) Drugs that have an influence on the status of sex hormones, e.g., additional hormonal treatments (either oral or transdermal) including estrogen, progesterone hormone replacement therapy including megestrol acetate, oral or other types of hormonal contraceptives (including implants and depot injections), hormonal stimulation of ovaries (i.e., oocytes cryopreservation, IVF or ICSI), selective estrogen modulators (e.g., basedoxifene, ospemifene, raloxifene, tamoxifen)
- (2) Patients receiving any prior systemic cancer therapy for invasive breast cancer
- (3) Patients with a history of any malignancy are ineligible except for the following circumstances: - Patients with a malignancy history other than invasive breast cancer if they have been disease-free for at least 5 years and are deemed by the investigator to be at low risk for recurrence of that malignancy; - Patients with a history of completely resected non-metastatic, non-melanoma skin cancer; - Patients with a history of successfully treated in situ carcinoma; - Patients with a contralateral breast carcinoma in situ; - - Patients with an ipsilateral breast carcinoma in situ (only in case in situ carcinoma is a separate lesion and not a component of the invasive breast cancer per histology report of biopsied invasive target lesion)
- (4) Pregnant or lactating women
- (5) Concurrent participation in another clinical trial with the same primary endpoint and/or concurrent participation in another clinical trial with a therapeutic investigational product
- (6) Known hypersensitivity to the study drugs or its excipients (incl. peanut and soy)
- (7) Patients unable to swallow normally and to take tablet and capsules (predictable poor compliance to oral treatment per investigator’s assessment)
- (8) Medical history or ongoing gastrointestinal disorders potentially affecting the absorption of elacestrant and/or ribociclib (e.g., uncontrolled ulcerative diseases, uncontrolled/refractory/chronic nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel/significant gastric resection)
- (9) Patient has had major surgery within 28 days prior to randomization or has not recovered from major side effects (as per investigator’s assessment)
The study team makes the final eligibility decision.
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18-64 years, 65+ years. The study team makes the final eligibility decision.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.