EUCTR2011-001119-30-NL进行中（未招募）不适用
An open-label, Phase I/IIa, dose escalating study of 2B3-101 in patients with solid tumors and brain metastases or recurrent malignant glioma. - 2B3-101-CR-001
to-BBB technologies B.V.0 个研究点目标入组 82 人开始时间: 2011年4月12日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 82
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •To be eligible to participate in this study, candidates must meet the following eligibility criteria:
- •1.Age = 18 years.
- •2.Measurable intracranial disease by MRI.
- •3.ECOG Performance Status = 2.
- •4.Estimated life expectancy of at least 8 weeks.
- •5.Toxicities incurred as a result of previous anticancer therapy (radiation therapy, chemotherapy, or surgery) must be resolved to = grade 2 (as defined by CTCAE version 4.0).
- •6.No evidence of (cortical) cognitive impairment as defined by a Mini-Mental Status Exam (MMSE) score = 25/30.
- •7.Written informed consent according to local guidelines.
- •In addition to the above listed eligibility criteria, the following criteria are applicable:
- •8.2B3-101 single agent dose-escalation phase:
- •Patients with pathologically confirmed diagnosis of advanced, recurrent solid tumors and unequivocal evidence of brain metastases that are refractory to standard therapy or for whom no standard therapy exists or with unequivocal evidence of newly diagnosed untreated brain metastases and controlled extracranial disease.
- •Patients with pathology confirmed diagnosis of advanced, recurrent primary malignant (grade III and IV) glioma that are refractory to standard therapy or for whom no standard therapy exists.
- •2B3-101 in combination with trastuzumab dose-escalation phase:
- •Patients with histologically-confirmed HER2-positive adenocarcinoma of the breast with unequivocal evidence of brain metastases that are refractory to standard therapy or for which no standard therapy exist or with unequivocal evidence of newly diagnosed untreated brain metastases and controlled extracranial disease.
- •Breast cancer brain metastases study- arm of the expansion phase:
- •Patients with pathologically confirmed diagnosis of advanced, recurrent breast cancer with unequivocal evidence of brain metastases that are refractory to standard therapy or for whom no standard therapy exist.
- •Patients with pathologically confirmed diagnosis of advanced breast cancer with newly diagnosed, untreated, brain metastases, which per multi-disciplinary team decision do not require immediate radiotherapy or surgery.
- •Patients with histologically-confirmed HER2-positive adenocarcinoma of the breast with unequivocal evidence of brain metastases that are refractory to standard therapy or for which no standard therapy exist or with unequivocal evidence of newly diagnosed untreated brain metastases, which per the multi-disciplinary team decision do not require immediate radiotherapy or surgery
- •SCLC brain metastases study arm of the expansion phase:
- •Patients with pathologically confirmed diagnosis of advanced, recurrent SCLC with unequivocal evidence of brain metastases that are refractory to standard therapy or for whom no standard therapy exist.
- •Patients with pathologically confirmed diagnosis of advanced SCLC with newly diagnosed, untreated, brain metastases, which per multi-disciplinary team decision do not require immediate radiotherapy or surgery.
- •Melanoma brain metastases study arm of the expansion phase:
- •- Patients with pathologically confirmed diagnosis of advanced, recurrent melanoma with unequivocal evidence of brain metastases that are refractory to standard therapy or for whom no standard therapy exist.
- •Patients with pathologically confirmed diagnosis of advanced mel;anoma with newly diagnosed, untreated, brain metastases, which per multi-disciplinary team decision do not require
排除标准
- •Candidates will be excluded from study entry if any of the following exclusion criteria exist:
- •Prior Treatment:
- •1.Less than 1 week since the last treatment of lapatinib, less than 2 weeks since the last treatment of vemurafenib, less than 4 weeks since the last treatment of chemotherapy, biological therapy, immunotherapy and systemicradiotherapy (except palliative radiation delivered to <20% of bone marrow), less than 6 weeks for nitrosoureas and mitomycin C and less than 8 weeks for cranial radiotherapy. Previous trastuzumab treatment will be allowed to continue without interruption in patients that are included in either the 2B3-101 dose-escalation phase in combination with trastuzumab or in the breast cancer expansion phase once the MTD for the combination has been established.
- •2.Patients that have received a maximum cumulative dose of free (i.e., non-liposomal) or liposomal doxorubicin > 360mg/m2 or free epirubicin > 600mg/m2
- •Current Treatment:
- •3.Current or recent (within 30 days of first study treatment) treatment with another investigational drug or participation in another investigational study.
- •Hematology, coagulation and biochemistry:
- •4.Inadequate bone marrow function: Absolute Neutrophil Count (ANC): < 1.5 x 109/L, or platelet count < 100 x 109/L or hemoglobin < 6 mmol/L.
- •5.Inadequate liver function, defined as:
- •Serum (total) bilirubin > 1.5 x the ULN for the institution if no liver metastases (> 2 x ULN in patients with liver metastases);
- •ASAT or ALAT > 2.5 x ULN if no liver metastases (> 4 x ULN in patients with liver metastases);
- •Alkaline phosphatase levels > 2.5 x ULN if no liver metastases (> 5 x ULN in patients with liver metastases, or > 10 x ULN in patients with bone metastases).
- •6.Inadequate renal function, defined as:
- •Serum creatinine > 1.5 x ULN.
- •7.Leptomeningeal carcinomatosis as the only site of CNS involvement.
- •8.Pregnancy or lactation. Serum pregnancy test to be performed within 7 days prior to study treatment start, or within 14 days followed by a confirmatory urine pregnancy test within 7 days prior to study treatment start.
- •9.For female subjects of childbearing potential (defined as < 2 years after last menstruation and not surgically sterile) and male subjects who are not surgically sterile or with female partners of childbearing potential: absence of effective, non-hormonal means of contraception (intrauterine contraceptive device, barrier method of contraception in conjunction with spermicidal gel).
- •10.Major surgical procedure (including open biopsy, excluding central line IV and portacath) within 28 days prior to the first study treatment, or anticipation of the need for major surgery during the course of the study treatment.
- •11.Grade 3 or 4 motor, sensory, or cranial neuropathy symptoms (as defined by CTCAE version 4.0).
- •12.Uncontrolled hypertension (systolic > 150 mm Hg and/or diastolic > 100mm Hg).
- •13.Clinically significant (i.e. active) cardiovascular disease defined as:
- •Stroke within = 6 months prior to day 1;
- •Transient Ischemic Attack (TIA) within = 6 months prior to day 1;
- •Myocardial infarction within = 6 months prior to day 1;
- •Unstable angina;
- •New York Heart Association (NYHA) Grade II or greater Congestive Heart Failure (CHF);
- •Serious cardiac arrhythmia requiring medication;
- •Clinically relevant pathologic findings in ECG.
- •14.14.Left Ventricle Ejection Fraction (LVEF) by MUGA or ECHO < 55% for patients recei
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