跳至主要内容
临床试验/PER-030-13
PER-030-13未知未知

A RANDOMIZED, DOUBLE-BLIND, PHASE 3 STUDY EVALUATING THE EFFICACY AND SAFETYOF ABP 980 COMPARED WITH TRASTUZUMAB IN SUBJECTS WITH HER2 POSITIVE EARLY BREAST CANCER

AMGEN INC.,0 个研究点目标入组 0 人开始时间: 2014年2月14日最近更新:
适应症

试验速览

阶段
未知
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 85(—)
性别
Female

入选标准

  • 8.3.1 Inclusion Criteria
  • Subjects MUST satisfy all of the following entry criteria before they will be allowed to participate in the study:
  • 1. Females ≥ 18 years old
  • 2. Histologically confirmed invasive breast cancer
  • 3. Planning for surgical resection of breast tumor and SN or axillary lymph node resection
  • 4. Planning neoadjuvant chemotherapy
  • 5. HER2 positive disease defined as:
  • o +3 overexpression by immunohistochemistry (IHC) or
  • o HER2 amplification by fluorescence in situ hybridization (FISH)
  • 6. Measurable disease ( assessment method used in order of priority: ultrasound, mammography, MRI, or physical examination) in the breast after diagnostic biopsy, defined as longest diameter ≥ 2.0 cm
  • 7. Known ER and PR hormone receptor status at study entry
  • 8. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • 9. Left ventricular ejection fraction (LVEF) of ≥ 55 % by 2D echocardiogram
  • (Others, please see Study Protocol)

排除标准

  • 8.3.2 Exclusion Criteria
  • If any of the following apply, the subject MUST NOT enter the study:
  • 1. Bilateral breast cancer
  • 2. Presence of know metastases
  • 3. Received prior treatment, including chemotherapy, biologic therapy, radiation or surgery with the exception of diagnostic biopsy for primary breast cancer
  • 4. Other concomitant active malignancy or history of malignancy in the past 5 years except treated basal cell carcinoma of the skin or carcinoma in situ of the cervix
  • 5. Pre-existing clinically significant (≥ grado 2) peripheral neuropathy
  • 6. Any history of documented or current congestive heart failure, current high-risk uncontrolled arrhythmias, current angina pectoris requiring a medicinal product, current clinically significant valvular disease, current evidence of transmural infarction on electrocardiogram (ECG) or current poorly controlled hypertension
  • 7. Severe dyspnea at rest requiring supplementary oxygen therapy
  • (Others, please see Study Protocol)

研究者

发起方
AMGEN INC.,

相似试验

进行中(未招募)
1 期
The trial is designed to determine the efficacy and safety of ABP 980 compared with Trastuzumab in subjects with HER2 positive early breast cancerHER2 Positive Early Breast CancerMedDRA version: 18.0Level: PTClassification code 10065430Term: HER-2 positive breast cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
EUCTR2012-004319-29-CZAmgen Inc.768
进行中(未招募)
不适用
The trial is designed to determine the efficacy and safety of ABP 215 compared with Bevacizumab in subjects with advanced non-small cell lung cancerAdvanced Non-small Cell Lung CancerMedDRA version: 17.0Level: PTClassification code 10061873Term: Non-small cell lung cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
EUCTR2013-000738-36-BGAmgen Inc.620
进行中(未招募)
1 期
The trial is designed to determine the efficacy and safety of ABP 980 compared with Trastuzumab in subjects with HER2 positive early breast cancerHER2 Positive Early Breast CancerMedDRA version: 14.1Level: LLTClassification code 10065430Term: HER-2 positive breast cancerSystem Organ Class: 100000004864
EUCTR2012-004319-29-ESAmgen Inc.556
尚未招募
3 期
A Randomized, Double-Blind, Phase 3 Study Evaluating the Safety and Efficacy of Venetoclax in Combination with Azacitidine in Patients Newly Diagnosed with Higher-Risk Myelodysplastic Syndrome (Higher-Risk MDS)Myelodisplastic Syndrome (MDS)myelodysplasia10024324
NL-OMON54378AbbVie Deutschland GmbH & Co. KG13
进行中(未招募)
1 期
Double-Blind study comparing venetoclax and azacitidine versus placebo and azacitidine in patients that are newly diagnosed with Higher-Risk Myelodysplastic SyndromeMyelodysplastic Syndrome
EUCTR2020-000744-55-FRAbbVie500