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Efficacy and Safety of Oral Treatment With BIBF 1120 ES in Advanced Non-small-cell Lung Cancer

2017年12月27日 更新者:Boehringer Ingelheim

A Double-blind, Randomised Phase II Study to Determine Efficacy and Safety of Oral Treatment With BIBF 1120 ES 250 mg Twice Daily Versus 150 mg Twice Daily in Patients Suffering From Advanced Non-small-cell Lung Cancer

The overall purpose of this phase II trial was to evaluate the efficacy of 250 mg BIBF 1120 twice daily (BID) versus 150 mg BIBF 1120 BID in patients with advanced non-small-cell lung cancer (NSCLC) who had failed at least one prior chemotherapy regimen. In addition, safety data for the two different dosages were collected and analysed.

研究概览

研究类型

介入性

注册 (实际的)

73

阶段

  • 阶段2

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion criteria:

  1. Male or female patients with histologically confirmed advanced NSCLC (i.e. adenocarcinoma, squamous cell carcinoma, large cell carcinoma, or combinations of these) stage IIIB (including pleural effusion) and stage IV.
  2. Patients with recurrent disease who relapsed after previous treatment with platinum- or non-platinum based chemotherapy.
  3. Full recovery from all therapy related toxicities from previous chemotherapy/ radiotherapy or recovery in as much as no further improvement may be expected by the investigator.
  4. Age ≥18 years.
  5. Life expectancy of at least 3 months.
  6. ECOG performance score 0, 1 or 2.
  7. Uni-dimensionally measurable tumour lesions by one or more techniques, i.e. CT, MRI, X-ray.
  8. Adequate hepatic function: total bilirubin within normal limits; alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) ≤ 1.5x upper limit of normal (ULN) in patients without liver metastasis; For patients with liver metastasis: total bilirubin ≤ 1.5x ULN; ALT and/or AST < 2.5x ULN.
  9. Coagulation parameters: international normalised ratio less than 1.3 or prothrombin time (PT) and partial thromboplastin time (PTT) less than 1.5 times institutional ULN.
  10. Adequate renal function: serum creatinine ≤ 1.5 x upper normal limit.
  11. Absolute neutrophil count (ANC) ≥ 1500/mL, platelets ≥ 100000/mL, haemoglobin ≥ 9.0 g/dL.
  12. Written informed consent consistent with ICH-GCP guidelines and local law.

Exclusion criteria:

  1. Active brain metastases stable for < 4 weeks, symptomatic, or requiring treatment with anti-convulsants and/or steroids or leptomeningeal disease.
  2. Patients with history of haemorrhagic or thrombotic event (including transient ischemic attacks) in the past 12 months. Known inherited predisposition to thrombosis.
  3. Concurrent therapeutic anticoagulation (except heparin flush as needed for maintenance of an indwelling intravenous device) or antiplatelet therapy (except chronic low-dose daily acetylsalicylic acid < 325mg).
  4. Sanguineous pleural effusion due to disease or pericardial effusion suspicious for disease.
  5. Clinically significant haemoptysis (1 teaspoon or more) within the last 3 months.
  6. Centrally located tumours with radiographic evidence (CT or MRI) of local invasion of major blood vessels.
  7. Radiographic evidence of cavitary or necrotic tumours at screening.
  8. Major injuries and surgeries. Planned surgical procedures during the trial. Patients with incomplete wound healing within the past 4 weeks.
  9. Gross haematuria within the last 3 months.
  10. Significant cardiovascular diseases (i.e. uncontrolled hypertension, unstable angina, history of myocardial infarction within the past 6 months, serious cardiac arrhythmia, congestive heart failure according to New York Heart Association (NYHA) III or IV.
  11. Serious illness or concomitant non-oncological disease such as neurologic-, psychiatric- or infectious disease 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.
  12. Gastrointestinal abnormalities that would interfere with intake or absorption of the study drug, prior surgical procedures affecting absorption, treatment for peptic ulcer disease within the last 6 months, active gastrointestinal bleeding unrelated to cancer (as evidenced by either hematemesis, hematochezia, or melena in the past 3 months and without endoscopic documented resolution), or malabsorption syndromes.
  13. Other malignancy within the past 5 years (other than non-melanomatous skin cancer or cervical carcinoma in situ).
  14. Treatment with other investigational drugs (elimination half life < 5 days) within the past 4 weeks before visit 2 or participation in another clinical trial within the past 4 weeks before start of therapy (visit 2) or concomitantly with this trial.
  15. Treatment with chemo-, immuno-, hormonotherapy or with biologic response modifier within the past four weeks prior to treatment with the trial drug and during the trial.
  16. Radiotherapy within the last 4 weeks prior start of treatment with the trial drug and radiotherapy to an area of measurable disease.
  17. Hypersensitivity to BIBF 1120 ES or the excipients of the trial drug.
  18. Male or female patients who are sexually active and unwilling to use a medically acceptable method of contraception prior to study entry and for the duration of study participation.
  19. Pregnancy or breast feeding.
  20. Known or suspected active alcohol or drug abuse.
  21. Patients unable to comply with the protocol.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:安慰剂
实验性的:BIBF 1120 ES low dose
实验性的:BIBF 1120 ES high dose

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Tumour response according to response evaluation criteria in solid tumours (RECIST)
大体时间:baseline, every 6 weeks for an expected mean observation duration of 9 months
baseline, every 6 weeks for an expected mean observation duration of 9 months
Time to tumour progression
大体时间:baseline, every 6 weeks for an expected mean observation duration of 9 months
baseline, every 6 weeks for an expected mean observation duration of 9 months

次要结果测量

结果测量
大体时间
Overall survival
大体时间:mean observation duration of 9 months
mean observation duration of 9 months
European Organization for Research and Treatment (EORTC) Quality of Life Questionnaire (QLQ) (EORTC QLQ-C30) score
大体时间:mean observation duration of 9 months
mean observation duration of 9 months
EORTC QLC lung cancer module (QLQ-LC13) score
大体时间:mean observation duration of 9 months
mean observation duration of 9 months
Incidence and intensity of adverse events, graded by Common Terminology Criteria (CTCAE) 3.0
大体时间:mean observation duration of 9 months
mean observation duration of 9 months
Changes in safety laboratory parameters
大体时间:mean observation duration of 9 months
mean observation duration of 9 months
Eastern Cooperative Oncology Group (ECOG) performance score
大体时间:mean observation duration of 9 months
mean observation duration of 9 months
Changes in vital signs (body temperature, blood pressure, pulse rate, respiratory rate)
大体时间:mean observation duration of 9 months
mean observation duration of 9 months
Maximum plasma concentration (Cmax)
大体时间:pre-dose, 1, 2, and 3 hours after administration
pre-dose, 1, 2, and 3 hours after administration
Area under the curve (AUC)
大体时间:pre-dose, 1, 2, and 3 hours after administration
pre-dose, 1, 2, and 3 hours after administration

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2005年8月1日

初级完成 (实际的)

2007年1月1日

研究注册日期

首次提交

2014年7月2日

首先提交符合 QC 标准的

2014年7月7日

首次发布 (估计)

2014年7月8日

研究记录更新

最后更新发布 (实际的)

2017年12月28日

上次提交的符合 QC 标准的更新

2017年12月27日

最后验证

2017年12月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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