NCT01251484已完成2 期
Phase II Study of BIBF 1120 in Recurrent Glioblastoma Multiforme
Ulrik Lassen2 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2011年1月1日最近更新:
适应症
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 25
- 试验地点
- 2
- 主要终点
- Response rate
研究概览
简要总结
VEGF inhibition by BEV may induce a change in tumor invasiveness and treatment failure is often associated with remote metastases. BEV may stop the growth of tumor cells by blocking blood flow to the tumor. Cediranib, a pan-VEGF inhibitor has shown promising results in recurrent GBM.
VEGF-blocking with small molecules may overcome the mechanism of resistance, and response to BIBF-1120 in such circumstances may open a new treatment option in GBM. In additional, recurrent glioblastomas have an extremely poor prognosis, so innovative therapies are needed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 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
- All
- 接受健康志愿者
- 否
入选标准
- •Written informed consent
- •Histological verification of primary GBM and failure after radiotherapy and TMZ
- •- Previously received radiotherapy and TMZ
- •More than 4 weeks since any of the following prior treatments
- •Chemotherapy (6 weeks for nitrosureas or mitomycin C)
- •Radiotherapy to nontarget lesions or lesions that are not to be biopsied
- •Investigational agents
- •More than 6 months since prior major surgery or open biopsy and recovered (only 6 weeks required if operation is for recurrent BGM)
- •● ECOG performance status 0-1
- •Age > 18 years
- •Creatinine normal OR creatinine clearance ≥ 60 mL/min
- •Fertile females must use anticonception (p- pills, IUD, depot injection of gestagen, subdermal
- •implantation, hormonal vaginal ring or transdermal depot plaster, throughout the study and 3
- •months after discontinuation of study drugs. Fertile men must use dobbelt barrier method
- •(preservative with sperm inhibiting creme) or female partner uses the above mentioned
- •contraception.
- •Fertile males must use preservatives.
- •Exclusions criteria
- •Prior treatment with BIBF 1120 or any other VEGFR inhibitor, except bevacizumab in Group 2
- •Chemo-, hormono-, radio-(except for brain and extremities) or immunotherapy or therapy with monoclonal antibodies or small tyrosine kinase inhibitors within the past 4 weeks prior to treatment with the trial drug.
- •Persistence of clinically relevant therapy related toxicity from previous chemo and/or radiotherapy
- •Treatment with other investigational drugs or treatment in another clinical trial within the past 4 weeks before start of therapy or concomitantly with the trial
- •Therapeutic anticoagulation( except low-dose heparin and/or heparin flush as needed for maintenance of an in-dwelling intravenous devise) or anti-platelet therapy (except for low-dose therapy with acetylsalicylic acid<325mg per day
- •Major injuries within the past 10 days prior to start of study treatment with incomplete wound healing and/or planned surgery during the on-treatment study period
- •History of clinically significant haemorrhagic or thromboembolic event in the past 6 months
- •Known inherited predisposition to bleeding or thrombosis
- •Significant cardiovascular diseases ( i.e. uncontrolled hypertension, unstable angina, history of infarction within the past 12 months prior to start of study treatment, congestive heart failure > NYHA II, serious cardiac arrhythmia, pericardial effusion)
- •Proteinuria CTCAE grade 2 or greater
- •Hepatic function: total bilirubin outside of normal limits; ALT or AST > 1.5 ULN
- •Coagulation parameters: International normalised ratio ( INR) > 2, prothrombin time
- •- (PT) and partial thromboplastin time (PTT) > 50% of deviation of institutional ULN
- •Absolute neutrophil count ( ANC) < 1500/ml, platelets < 100000/ml, Haemoglobin < 9.0 g/dl
- •Other malignancies within the past 5 years other then basal cell skin cancer or carcinoma in situ of the cervix
- •Active serious infections in particular if requiring systemic antibiotic or antimicrobial therapy
- •Active or chronic hepatitis C and/or B infection
- •Gastrointestinal disorders or abnormalities that would interfere with absorption of the study drug
- •Serious illness or concomitant non-oncological disease such as neurologic, psychiatric, infectious disease or active ulcers (gastro-intestinal tract, skin) or laboratory abnormality that may increase the risk associated with study participation or study drug administration and in the judgment of the investigator would make the patient inappropriate for entry into the study.
- •Pregnancy or breast feeding
- •Psychological, familial, sociological or geographical factors potentially hampering compliance with the study protocol and follow-up schedule
- •active alcohol or drug abuse
排除标准
- 未提供
结局指标
主要结局
Response rate
时间窗: Response evaluation every 8 weeks
MacDonald criteria
次要结局
- Adverse events(Assessed every 2 weeks)
研究者
Ulrik Lassen
Ulrik Lassen, MD, PH.D
Rigshospitalet, Denmark
研究点 (2)
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