Phase II Study for Repeated Dosing of the Trifunctional Bispecific Anti-HER-2/Neu x Anti-CD3 Antibody Ertumaxomab in Patients With HER-2/Neu 1+ or 2+/FISH Negative Expressing Advanced or Metastatic Breast Cancer (Stage IIIb/IV) Progressing After Endocrine Treatment
试验速览
- 阶段
- 2 期
- 状态
- 终止
- 发起方
- 入组人数
- 40
- 试验地点
- 5
- 主要终点
- Clinical efficacy measured by objective response rate (best response during the course of the study)
研究概览
简要总结
The purpose of the study is to demonstrate clinical efficacy of the investigational trifunctional bispecific antibody ertumaxomab for treatment of patients with HER-2/neu 1+ or 2+ (FISH-) expressing advanced or metastatic breast cancer (stage III b/IV) which has progressed after endocrine therapy.
Ertumaxomab is a trifunctional bispecific antibody targeting Her-2/neu and CD3 on T cells. Trifunctional antibodies represent a new concept for targeted anticancer therapy. This new antibody class has the capability to redirect T cells and accessory cells (e.g. macrophages, dendritic cells [DCs] and natural killer [NK] cells) to the tumor site. According to preclinical data, trifunctional antibodies activate these immune cells, which can trigger a complex anti-tumor immune response.
详细描述
An open-label, non-randomized, uncontrolled, one-stage, phase II study evaluating the efficacy and safety of the investigational trifunctional bispecific antibody ertumaxomab (anti-Her-2/neu x anti-CD3) for the treatment of hormone therapy refractory advanced or metastatic breast cancer tumours (stage IIIb or IV) which are known to express HER-2/neu (1+ or 2+/FISH negative).Ertumaxomab will be administered at 7 day intervals by constant rate 3 hour intravenous (i.v.) infusions according to the following sequential dose schedule: 10 µg (day 0) and thereafter 100 µg flat doses once every 7 days (± 1 day) for a maximum of up to 12 weeks or until disease progression or any other unacceptable toxicity.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Signed and dated informed consent form
- •Women ≥ 18 years, negative pregnancy test at screening life expectancy of at least 6 months
- •Locally advanced (stage IIIb) or metastatic (stage IV) and not curable adenocarcinoma of the breast
- •Measurable disease, defined as at least one lesion that is measurable in one dimension (RECIST)
- •HER-2/neu expression 1+ or 2+ / FISH negative
- •Estrogen Receptors (ERs) and/or Progesterone Receptors (PRs) positive
- •Prior adequate endocrine therapy for advanced or metastatic disease
- •Disease progression during or after endocrine therapy
- •No prior treatment with mouse or rat antibodies
- •ECOG performance score of ≤ 1
- •Adequate hematological, liver and kidney function
排除标准
- •Women who are pregnant or breast-feeding
- •Known HIV infection or Presence of autoimmune disease or other Concurrent non-malignant co-morbidities that are uncontrolled
- •History or symptoms indicative of brain or CNS metastases
- •Prior diagnosis of any malignancy not cured by surgery alone less than 5 years before study entry (except in situ carcinoma of the cervix or adequately treated basal cell carcinoma of the skin)
- •Documented acute or chronic infection requiring antibiotic treatment
- •Any concurrent chemo-, hormonal, immuno- or corticoid therapy
- •Any prior chemotherapy for advanced or metastatic disease
- •Any concurrent investigational treatment for advanced or metastatic disease
- •History of relevant cardiovascular disease as follows:
- •Left ventricular ejection fraction (LVEF) below the institution's lower limit of normal, based on echocardiography (ECG) at rest
- •Uncontrolled or symptomatic congestive heart failure (New York Heart Association (NYHA) > 2
- •Uncontrolled or symptomatic arrhythmia and/or angina pectoris
- •Myocardial infarction during the last 2 years
结局指标
主要结局
Clinical efficacy measured by objective response rate (best response during the course of the study)
次要结局
- Duration of response
- Time to progression (TTP)
- Efficacy:
- Clinical benefit rate
- Incidence of adverse events (AEs)
- Vital signs
- Laboratory parameters
- Safety:
- Presence of human anti-murine antibodies after ertumaxomab infusion