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A Study of CriPec® Docetaxel Given to Patients With Solid Tumours (NAPOLY)

2018年9月21日 更新者:Cristal Therapeutics

A Phase I Open-Label, Safety, Pharmacokinetic and Preliminary Efficacy Study of CriPec® Docetaxel in Patients With Solid Tumours

The goal of this Phase1 clinical research study is to find the highest safe dose of CriPec® docetaxel that can be given in the treatment of patients with solid tumours.

研究概览

地位

完全的

详细说明

The study is designed to explore the safety, tolerability, pharmacokinetics and pharmacodynamics of CriPec® docetaxel and to identify the Maximum Tolerated Dose (MTD).

研究类型

介入性

注册 (实际的)

33

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

      • Leuven、比利时
        • University Hospital Leuven
      • Amsterdam、荷兰
        • VUMC Amsterdam
      • Groningen、荷兰
        • UMC Groningen
      • Rotterdam、荷兰
        • Erasmus Medical Center

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

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. At least 18 years old
  2. Eastern Cooperative Oncology Group (ECOG) Performance Status 0 or 1
  3. Estimated life expectancy of at least 12 weeks
  4. Ability and willingness to give written informed consent and to comply with the requirements of the study

    For Part 1:

  5. Patients with pathologically confirmed diagnosis of advanced, recurrent and progressive solid tumours that are refractory to standard therapy or for whom no standard therapy exists and with measurable or evaluable disease according to RECIST 1.1.

    For Part 2:

  6. Patients with pathologically confirmed diagnosis of advanced, recurrent and progressive cancer with measurable disease according to RECIST 1.1 of a histological type that are refractory to standard therapy or for whom no standard therapy exists and where treatment with a taxane is an appropriate treatment option.

Exclusion Criteria:

  1. Less than 4 weeks since the last treatment of chemotherapy, biological therapy, immunotherapy or systemic radiotherapy (except palliative radiation delivered to <20% of bone marrow), and less than 6 weeks for nitrosoureas and mitomycin C prior to Cycle 1 Day 1.
  2. Current or recent (within 4 weeks prior to Cycle 1 Day 1) treatment with another Investigational Product or participation in another investigational interventional study.
  3. Symptomatic brain metastases.
  4. Toxicities incurred as a result of previous anticancer therapy (radiation therapy, chemotherapy, or surgery) that have not resolved to ≤ grade 2 (as defined by CTCAE version 4.03).
  5. Inadequate bone marrow function at screening as evidenced by any of the following:

    • Absolute Neutrophil Count (ANC) < 1.5 x 109/L.
    • Platelet count < 100 x 109/L.
    • Haemoglobin < 6.0 mmol/L (< 9.6 g/dL). The patient should not have received a transfusion or growth factors for these abnormalities in the 7 days prior to Cycle 1 Day 1.
  6. Serum (total) bilirubin > 1.5 x the Upper Limit of Normal (ULN) for the institution if no liver metastases (> 2 x ULN in patients with liver metastases).
  7. AST or ALT > 2.5 x ULN if no liver metastases (> 5x ULN in patients with liver metastases).
  8. 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).
  9. Increased plasma prothrombin time or International Normalized Ratio (INR), consequence of reduced hepatic production of Vitamin K.
  10. Hepatitis B surface antigen or hepatitis C positivity with abnormal liver function tests.
  11. Medical history of:

    • Nonalcoholic steatohepatitis (NASH).
    • History of human immunodeficiency virus (HIV) antibody positive or use of antiretroviral therapy.
    • Alcoholic and autoimmune hepatitis.
    • Ischemic hepatitis, Cardiovascular dysfunction or impaired liver oxygenation, including hypotension or right heart failure.
  12. Serum creatinine > 1.5 x ULN.
  13. Estimated Glomerular Filtration Rate of < 50 mL/min/1.73m2 calculated by Modification of Diet in Renal Disease (MDRD) formula or creatinine clearance of < 50 mL/min calculated by Cockcroft-Gault.
  14. Stroke within 6 months prior to Cycle 1 Day 1.
  15. Transient Ischemic Attack (TIA) within 6 months prior to Cycle 1 Day 1.
  16. Myocardial infarction within 6 months prior to Cycle 1 Day 1.
  17. Unstable angina.
  18. New York Heart Association (NYHA) Grade II or greater Congestive Heart Failure at screening.
  19. Serious cardiac arrhythmia requiring medication.
  20. Patients who are pregnant or breastfeeding.
  21. Absence of effective means of contraception in female patients of childbearing potential (defined as <2 years after last menstruation and not surgically sterile) or in male patients who are not surgically sterile and who have female partners of childbearing potential.
  22. Major surgical procedure (including open biopsy and excluding central line intravenous catheter) within 28 days prior to the first study treatment, or anticipation of the need for major surgery during the course of the study treatment.
  23. Grade ≥2 motor or sensory neuropathy symptoms (as defined by CTCAE version 4.03).
  24. Known hypersensitivity to any of the Investigational Product's excipients or taxanes.
  25. History of drug or alcohol abuse in the opinion of the investigator within 3 years before screening.
  26. Evidence of any other medical conditions (such as psychiatric illness, infectious diseases, physical examination or laboratory findings) that may interfere with the planned treatment, affect patient compliance or place the patient at high risk for treatment-related complications.

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:不适用
  • 介入模型:单组作业
  • 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:CriPec® docetaxel
Docetaxel containing nanoparticle
-3 weekly IV dose. Dose escalation; start dose 15 mg/m2. Number of cycles: 6 or until progression or unacceptable toxicity develops
其他名称:
  • Docetaxel containing nanoparticles

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
Part 1: Incidence of grade 3 or 4 adverse events (AEs) as a measure of safety and tolerability.
大体时间:9 months
Part 1: Incidence of grade 3 or 4 adverse events (AEs) will be determined after escalating doses of CriPec® docetaxel once every three weeks.
9 months
Part 1: Incidence of clinical laboratory abnormalities as a measure of safety and tolerability.
大体时间:9 months
Part 1: Incidence of laboratory abnormalities will be determined after escalating doses of CriPec® docetaxel once every three weeks.
9 months
Part 1: Incidence of electrocardiogram (ECG) abnormalities as a measure of safety and tolerability.
大体时间:9 months
Part 1: Incidence of electrocardiogram (ECG) abnormalities will be determined after escalating doses of CriPec® docetaxel once every three weeks.
9 months
Part 2: Incidence of grade 3 or 4 adverse events (AEs) at the Maximum Tolerated Dose (MTD) of CriPec® docetaxel as defined in Part 1.
大体时间:9 months
Part 2: Incidence of grade 3 or 4 adverse events (AEs) at the Maximum Tolerated Dose will be determined after CriPec® docetaxel dosing once every three weeks.
9 months
Part 2: Incidence of clinical laboratory abnormalities at the Maximum Tolerated Dose (MTD) of CriPec® docetaxel as defined in Part 1
大体时间:9 months
Part 2: Incidence of clinical laboratory abnormalities at the Maximum Tolerated Dose will be determined after CriPec® docetaxel dosing once every three weeks.
9 months
Part 2: Incidence of electrocardiogram (ECG) abnormalities at the Maximum Tolerated Dose (MTD) of CriPec® docetaxel as defined in Part 1
大体时间:9 months
Part 2: Incidence of electrocardiogram (ECG) abnormalities at the Maximum Tolerated Dose will be determined after CriPec® docetaxel dosing once every three weeks.
9 months
Part 1 and 2: Pharmacokinetic profile of CriPec® docetaxel following IV infusion
大体时间:First two cycles of CriPec® docetaxel (each cycle is 3 weeks)
Pharmacokinetic parameters such as time to peak concentration (Tmax), peak concentration (Cmax), volume of distribution (Vd), half life (t1/2), total body clearance (CL) and area under the concentration-time curve (AUC) will be determined using plasma concentration data.
First two cycles of CriPec® docetaxel (each cycle is 3 weeks)

次要结果测量

结果测量
大体时间
Early signs of anti-tumor efficacy (overall response rate [ORR]) of CriPec® docetaxel
大体时间:18 months in total for part 1 and 2
18 months in total for part 1 and 2
Early signs of anti-tumor efficacy (duration of response) of CriPec® docetaxel
大体时间:18 months in total for part 1 and 2
18 months in total for part 1 and 2

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)

2015年8月1日

初级完成 (实际的)

2018年7月1日

研究完成 (实际的)

2018年7月1日

研究注册日期

首次提交

2015年5月1日

首先提交符合 QC 标准的

2015年5月8日

首次发布 (估计)

2015年5月13日

研究记录更新

最后更新发布 (实际的)

2018年9月24日

上次提交的符合 QC 标准的更新

2018年9月21日

最后验证

2018年7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.

CriPec® docetaxel的临床试验

3
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