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Study Evaluating Safety And Tolerability, Solid Tumor

2018年4月24日 更新者:Puma Biotechnology, Inc.

A Phase 1 Study Of Neratinib (HKI-272) In Combination With Paclitaxel In Subjects With Solid Tumors

This is an open-label, phase 1 study of ascending multiple oral doses of HKI-272 in combination with paclitaxel.

研究概览

研究类型

介入性

注册 (实际的)

10

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Shizuoka、日本
        • Investigational Site
      • Tokyo、日本
        • Investigational Site

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

20年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Subjects must have confirmed pathologic diagnosis of a solid tumor that is not curable with available therapy for which HKI-272 plus paclitaxel is a reasonable treatment option.
  • At least 1 measurable lesion as defined by RECIST criteria.
  • Eastern Cooperative Oncology Group (ECOG) 0 to 1
  • LVEF within institutional limits of normal (by MUGA or ECHO).
  • Screening laboratory values within the following parameters:

    • ANC: greater than or equal to 1.5 x 10E9 /L (1,500 /mm3)
    • Platelet count: 10 x 10E10 /L (100,000 /mm3)
    • Hemoglobin: greater than or equal to 9.0 g/dL
    • Serum creatinine: less than or equal to 1.5 x upper limit of normal (ULN)
    • Total bilirubin: less than or equal to 1.5 xULN · AST and ALT: less than or equal to 2.5 xULN (less than or equal to 5 x ULN if liver metastases are present)
  • For women of child bearing potential, a negative urine or serum pregnancy test result before study entry. A woman of childbearing potential is one who is biologically capable of becoming pregnant. This includes women who are using contraceptives or other means of birth control or whose sexual partners are either sterile or using contraceptives.
  • All subjects who are not surgically sterile or postmenopausal must agree and commit to the use of a reliable method of birth control for the duration of the study and for 28 days after the last dose of test article.

Exclusion Criteria:

  • Prior treatment with anthracyclines with a cumulative dose of doxorubicin of greater than 400 mg/m^2, epirubicin dose of greater than 800 mg/m^2, or the equivalent dose for other anthracyclines or derivatives.
  • Major surgery, chemotherapy, radical (curative intent) radiotherapy, investigational agents, or other cancer therapy within 2 weeks of treatment day 1 or non-recovery from all clinically significant acute adverse effects of prior therapies (excluding alopecia).
  • Subjects with bone or skin as the only site of disease.
  • Active central nervous system (CNS) metastases, as indicated by clinical symptoms, cerebral edema, and/or progressive growth (subjects with a history of CNS metastases or cord compression are allowable if they have been definitively treated and have been clinically stable for at least three months, and off steroids or anticonvulsants, before first dose of test article).
  • QTc interval greater than 0.47 second or known history of QTc prolongation or Torsade de Pointes (TdP).
  • Known hypersensitivity to paclitaxel or Cremophor EL (polyoxyethylated castor oil).
  • Pregnant or breast feeding women.
  • Significant chronic or recent acute gastrointestinal disorder with diarrhea as a major symptom (e.g., Crohn's disease, malabsorption, or Grade greater than or equal to 2 diarrhea of any etiology at baseline).
  • Inability or unwillingness to swallow the HKI-272.
  • Treatment with a taxane within 3 months of treatment day 1.
  • Pre-existing grade 2 or greater motor or sensory neuropathy.
  • Any other cancer within 5 years prior to screening with the exception of contralateral breast carcinoma, adequately treated cervical carcinoma in situ, or adequately treated basal or squamous cell carcinoma of the skin.
  • Presence of clinically significant or uncontrolled cardiac disease, including congestive heart failure (New York Heart Association [NYHA] functional classification of greater than or equal to 2), angina requiring treatment, myocardial infarction within the past 12 months, or any clinically significant supraventricular arrhythmia or ventricular arrhythmia requiring treatment or intervention.
  • Evidence of significant medical illness or abnormal laboratory finding that would, in the investigator's judgment, make the subject inappropriate for this study. Examples include, but are not limited to, serious active infection (ie, requiring intravenous antibiotic or antiviral agent), uncontrolled major seizure disorder, or significant pulmonary disorder (e.g. interstitial pneumonitis, pulmonary hypertension).

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:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Nera 160 + Pac
Neratinib 160 mg + Paclitaxel 80 mg/m^2
Administered orally, continuous, once daily.
其他名称:
  • HKI-272
Administered IV, on days 1, 8, 15 of 28 day cycle.
实验性的:Nera 240 + Pac
Neratinib 240 mg + Paclitaxel 80 mg/m^2
Administered orally, continuous, once daily.
其他名称:
  • HKI-272
Administered IV, on days 1, 8, 15 of 28 day cycle.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Dose Limiting Toxicity (DLT) - Percentage of Participants With DLT Events
大体时间:From first dose day through day 28.
The incidence of DLTs in subjects with advanced solid tumors, treated with neratinib in combination with paclitaxel 80 mg/m^2. DLT was defined as any neratinib plus paclitaxel related Grade 3 or 4 nonhematologic toxicity or Grade 4 hematologic toxicity with few exceptions.
From first dose day through day 28.
Maximum Tolerated Dose
大体时间:From first dose day through day 28.
The maximum tolerated dose of neratinib, as determined by the incidence of DLTs, in combination with paclitaxel 80 mg/m^2, in subjects with advanced solid tumors.
From first dose day through day 28.

次要结果测量

结果测量
措施说明
大体时间
Objective Response Rate
大体时间:From first dose date to progression/death or last tumor assessment, up to 78 weeks.
Percentage of participants with partial response (PR) or complete response (CR) per Response Evaluation Criteria In Solid Tumors Criteria (RECIST) v.1.0: Complete Response (CR), disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; and Non-PD for non-target lesions, and no new lesions.
From first dose date to progression/death or last tumor assessment, up to 78 weeks.
Progression Free Survival
大体时间:From first dose date to progression/death, up to 78 weeks.
Number of weeks between the date of the first dose of test article and the first date of disease recurrence or progression, or death due to any cause, was documented, censored at the last evaluation, investigator assessment. Progression is defined using Response Evaluation Criteria in Solid Tumors Criteria (v1.0), as at least a 20% increase in the sum of the longest diameters (LD) of target lesions, taking as reference the nadir LD, meaning the smallest sum of the LDs recorded since the treatment started; or unequivocal progression of existing nontarget lesions; or the appearance of any new lesions.
From first dose date to progression/death, up to 78 weeks.
Duration of Response
大体时间:From start date of response to first disease progression, up to 71 weeks.
Number of weeks from the time at which measurement criteria are met for Complete Response (CR) or Partial Response (PR) (whichever status is recorded first) until the first date on which recurrence or progressive disease (PD) is objectively documented, taking as reference for PD the smallest measurements recorded since the treatment started, for responders only, per Response Evaluation Criteria In Solid Tumors Criteria (RECIST) v.1.0: CR, disappearance of all target lesions; PR, >=30% decrease in the sum of the longest diameter of target lesions; and Non-PD for non-target lesions, and no new lesions.
From start date of response to first disease progression, up to 71 weeks.

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。

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 (实际的)

2008年10月1日

初级完成 (实际的)

2011年1月1日

研究完成 (实际的)

2011年1月1日

研究注册日期

首次提交

2008年10月7日

首先提交符合 QC 标准的

2008年10月7日

首次发布 (估计)

2008年10月8日

研究记录更新

最后更新发布 (实际的)

2018年11月19日

上次提交的符合 QC 标准的更新

2018年4月24日

最后验证

2018年4月1日

更多信息

与本研究相关的术语

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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