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A Study to Evaluate the Pharmacokinetics, Efficacy, and Safety of Subcutaneous Administration of the Fixed-Dose Combination of Pertuzumab and Trastuzumab in Combination With Chemotherapy in Participants With HER2-Positive Early Breast Cancer
Cancer Breast Cancer Early Breast Cancer
Basic Details
Sponsor
Hoffmann-La Roche
Phase
Phase 3
Study Identifier
NCT03493854, WO40324, 2017-004897-32
Condition
Early Breast Cancer
Official Title
A Phase III, Randomized, Multicenter, Open-Label, Two-Arm Study to Evaluate the Pharmacokinetics, Efficacy, and Safety of Subcutaneous Administration of the Fixed-Dose Combination of Pertuzumab and Trastuzumab in Combination With Chemotherapy in Patients With HER2-Positive Early Breast Cancer
Study Summary
This is a global Phase III, two-arm, open-label, multicenter, randomized study to investigate the pharmacokinetics, efficacy, and safety of the fixed-dose combination (FDC) of pertuzumab and trastuzumab for subcutaneous (SC) administration in combination with chemotherapy in patients with human epidermal growth factor receptor 2 (HER2)-positive early breast cancer in the neoadjuvant/adjuvant setting.
Eligibility Criteria
All
≥ 18 Years
No
Inclusion Criteria
- Ability to comply with the study protocol, in the investigator's judgment
- Eastern Cooperative Oncology Group (ECOG) Performance Status ≤1
- Female and male patients with Stage II - IIIC (T2-T4 plus any N, or any T plus N1-N3, M0), locally advanced, inflammatory, or early-stage, unilateral, and histologically confirmed invasive breast cancer
- Primary tumor >2 cm in diameter, or node-positive disease (clinically or on imaging, and node positivity confirmed with cytology and/or histopathology)
- HER2-positive breast cancer confirmed by a central laboratory prior to study enrollment. HER2-positive status will be determined based on pretreatment breast biopsy material.
- Hormone receptor status of the primary tumor, centrally confirmed
- Patient agreement to undergo mastectomy or breast conserving surgery after neoadjuvant therapy
- Availability of formalin-fixed, paraffin-embedded (FFPE) tumor tissue block for central confirmation of HER2 and hormone receptor status and additional biomarker research
- Baseline left ventricular ejection fraction (LVEF) ≥55% measured by echocardiogram (ECHO) or multiple-gated acquisition scan (MUGA)
- For women of childbearing potential (WOCBP) who are sexually active: agreement to remain abstinent or use one highly effective non-hormonal contraceptive method with a failure rate of <1% per year, or two effective non-hormonal contraceptive methods during the treatment period and for 7 months after the last dose of HER2-targeted therapy, and agreement to refrain from donating eggs during this same period
- For men: men must remain abstinent or use a condom with a spermicidal product during the treatment period and for 7 months after the last dose of HER2-targeted therapy to avoid exposing the embryo. Men must refrain from donating sperm during this same period.
- A negative serum pregnancy test must be available prior to randomization for WOCBP, unless they have undergone surgical sterilization
- No major surgical procedure unrelated to breast cancer within 28 days prior to randomization or anticipation of the need for major surgery during the course of study treatment
Exclusion Criteria
- Stage IV (metastatic) breast cancer
- Patients with a history of invasive breast cancer
- Patients with a history of concurrent or previously treated non-breast malignancies except for appropriately treated 1) non-melanoma skin cancer and/or 2) in situ carcinomas, including cervix, colon, and skin
- Patients who have received any previous systemic therapy for treatment or prevention of breast cancer, or radiation therapy for treatment of cancer
- Patients who have a past history of ductal carcinoma in situ or lobular carcinoma in situ if they have received any systemic therapy for its treatment or radiation therapy to the ipsilateral breast
- Patients with high-risk for breast cancer who have received chemo-preventative drugs in the past are not allowed to enter the study
- Patients with multicentric breast cancer, unless all tumors are HER2-positive
- Patients with bilateral breast cancer
- Patients who have undergone an excisional biopsy of primary tumor and/or axillary lymph nodes
- Axillary lymph node dissection prior to initiation of neoadjuvant therapy
- Sentinel lymph node biopsy prior to neoadjuvant therapy
- Treatment with any investigational drug within 28 days prior to randomization
- Serious cardiac illness or medical conditions
- Inadequate bone marrow function, renal function or impaired liver function
- Current severe, uncontrolled systemic disease that may interfere with planned treatment
- Pregnant or breastfeeding, or intending to become pregnant during the study or within 7 months after the last dose of HER2-targeted therapy
- Any serious medical condition or abnormality in clinical laboratory tests that, in the investigator's judgment, precludes the patient's safe participation in and completion of the study
- Known active liver disease, for example, active viral hepatitis infection, autoimmune hepatic disorders, or sclerosing cholangitis
- Concurrent, serious, uncontrolled infections, or known infection with HIV
- Known hypersensitivity to study drugs, excipients, and/or murine proteins
- Current chronic daily treatment with corticosteroids
- History of other malignancy within 5 years prior to screening, except for appropriately treated carcinoma in situ of the cervix, colon, skin, and/or non-melanoma skin carcinoma
- History of ventricular dysrhythmias or risk factors for ventricular dysrhythmias, such as structural heart disease, coronary heart disease, clinically significant electrolyte abnormalities, or family history of sudden unexplained death or long QT syndrome
The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical study see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.
The information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.
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Study results
LPS_WO40324_FeDeriCA_interim results_December2020_Chinese Traditional_Taiwan
(PDF, 1.1 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Czech
(PDF, 0.7 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Dutch_Belgium
(PDF, 0.5 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_English
(PDF, 2.0 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_French_Belgium
(PDF, 0.7 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_French_Canada
(PDF, 0.9 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_German
(PDF, 0.6 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Italian
(PDF, 0.5 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Japanese
(PDF, 0.6 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Korean
(PDF, 0.5 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Polish
(PDF, 0.5 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Portuguese_Brazil
(PDF, 1.2 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Russian
(PDF, 0.2 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Spanish_Argentina
(PDF, 1.6 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Spanish_Mexico
(PDF, 0.5 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Spanish_Spain
(PDF, 0.5 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Thai_Thailand
(PDF, 1.6 MB)
LPS_WO40324_FeDeriCA_interim results_December2020_Ukrainian
(PDF, 1.0 MB)
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For the latest version of this information please go to www.forpatients.roche.com