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Efficacy/Safety of Imprime PGG® Injection With Bevacizumab and Paclitaxel/Carboplatin in Patients With Untreated Advanced Non-Small Cell Lung Cancer (NSCLC)

2017年3月1日 更新者:HiberCell, Inc.

A Phase 2, Randomized, Efficacy and Safety Study of Imprime PGG® Injection in Combination With Bevacizumab and Concomitant Paclitaxel and Carboplatin Therapy in Patients With Previously Untreated Advanced (Stage IIIB or IV) Non-Small Cell Lung Cancer

The Phase 2 study described in this protocol will serve to evaluate the antitumor activity, safety and pharmacokinetic profile of Imprime PGG when combined with bevacizumab and concomitant paclitaxel and carboplatin therapy in patients with previously untreated advanced NSCLC. Additionally, this study will provide guidance for the design of more definitive efficacy studies of Imprime PGG in NSCLC patients.

研究概览

研究类型

介入性

注册 (实际的)

90

阶段

  • 阶段2

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

      • Halle/Saale、德国
        • Hospital Marth-Maria Halle Dolau
      • Kassel、德国
        • Clinical Kassel GmbH
      • Köln、德国
        • Kliniken der Stadt Koln gGmbH
      • Mainz、德国
        • University of Mainz
      • Munich、德国
        • University of Munich
      • Oldenburg、德国
        • Pius-Hospital Oldenburg
      • Ulm、德国、89081
        • Universitätsklinikum Ulm
    • Arkansas
      • Fayetteville、Arkansas、美国、72703
        • Highlands Oncology Group
    • Ohio
      • Canton、Ohio、美国、44718
        • Gabrail Cancer Center
    • Texas
      • San Antonio、Texas、美国、78229
        • University of Texas Health Science Center, San Antonio

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 至 75年 (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. Has read, understood and signed the informed consent form (ICF) approved by the Independent Review Board/Ethics Committee (IRB/EC);
  2. Is between the ages of 18 and 75 years old, inclusive;
  3. Has histologically or cytologically confirmed stage IIIB (malignant pericardial or pleural effusion) or stage IV non-small cell lung cancer;
  4. Has non-squamous, non-small cell lung cancer
  5. Has measurable disease, defined as at least one tumor that fulfills the criteria for a target lesion according to RECIST;
  6. Has an ECOG performance status of 0 or 1;
  7. Has a life expectancy of > 3 months;
  8. Has adequate hematologic function as evidenced by:

    1. ANC ≥ 1,500/μL
    2. PLT ≥ 100,000/μL
    3. HGB ≥ 9 g/dL obtained within 1 week prior to the first dose of study medication;
  9. Has adequate renal function as evidenced by:

    1. Serum creatinine ≤ 1.5 X the upper limit of normal (ULN) for the reference lab
    2. Urine dipstick for proteinuria of < 1+ (i.e., either 0 or trace) within 2 weeks of Day 1 If urine dipstick is ≥ 1+, then urine protein excretion must be ≤ 500 mg over a 24 hour collection obtained within 1 week prior to the first dose of study medication;
  10. Has adequate hepatic function as evidenced by:

    1. Serum total bilirubin ≤ 1.0 mg/dL
    2. AST ≤ 2.5X ULN for the reference lab (≤ 5X ULN for subjects with known hepatic metastases)
    3. ALT ≤ 2.5X ULN for the reference lab (≤ 5X ULN for subjects with known hepatic metastases) obtained within 1 week prior to the first dose of study medication;
  11. Has adequate coagulation function as evidenced by:

    1. INR ≤ 1.5
    2. PTT ≤ ULN for the reference lab obtained within 1 week prior to the first dose of study medication;
  12. If a woman of childbearing potential or a fertile man (and his partners), must agree to use an effective form of contraception (hormonal contraceptive, double-barrier method or abstinence) during the study.

Exclusion Criteria:

  1. Has received prior systemic chemotherapy at any time for lung cancer;
  2. Has received previous radiation therapy to >30% of active bone marrow or any radiation therapy within 3 weeks of Day 1;
  3. Has a known hypersensitivity to baker's yeast, or has an active yeast infection;
  4. Has had previous exposure to Betafectin® or Imprime PGG;
  5. Has an active infection;
  6. Presents with any of the following medical diagnoses/conditions at the time of screening:

    1. Central nervous system (CNS) metastases
    2. Uncontrolled hypertension (>150/100 mmHg) or hypertension that requires > two agents for adequate control
    3. Peripheral neuropathy ≥ grade 2 from any cause
    4. Fever of >38.5° C within 3 days prior to screening or Day 1, initial dosing
    5. Known HIV/AIDs, Hepatitis B, Hepatitis C, connective tissue or autoimmune disease, or other clinical diagnosis, ongoing or intercurrent illness that in the physician's opinion could interfere with participation
  7. Has a history of any of the following medical diagnoses/conditions:

    1. Arterial or venous thromboembolic or hemorrhagic disorders including stroke, transient ischemic attack or cerebral infarction
    2. Deep vein thrombosis within 1 year prior to screening
    3. Myocardial infarction or an unstable or uncontrolled disease or condition related to or impacting cardiac function (e.g., unstable angina, congestive heart failure) within the previous 6 months
    4. Second malignancy within the previous 5 years, other than basal cell carcinoma, cervical intra-epithelial neoplasia or curatively treated prostate cancer with a PSA of <2.0 ng/mL
  8. Has a known hypersensitivity to bevacizumab, murine proteins, or any component of bevacizumab;
  9. Has a know sensitivity to polyethoxylated castor oil;
  10. Has previously received treatment with bevacizumab;
  11. Has had surgery within 4 weeks of Day 1 or needle or open biopsy within 1 week of Day 1;
  12. Has a non-healing wound or gastric ulcer;
  13. Has a non-healed bone fracture;
  14. Is receiving systemic anti-coagulation therapy (e.g., dipyridalmole (Persantine®), ticlopidine (Ticlid®), clopidogrel (Plavix®) and /or cilostazol (Pletal®);
  15. Is receiving chronic daily treatment with aspirin (>100 mg/day) or other nonsteroidal anti-inflammatory agents known to inhibit platelet function within 1 week of Day 1;
  16. Presents with any of the following medical diagnoses/conditions at the time of screening:

    a. Predominant squamous cell histology

  17. Has a history of any of the following medical diagnoses/conditions:

    1. Hemoptysis (≥ ½ tsp red blood)
    2. Bleeding diathesis or coagulopathy
  18. If female, is pregnant or breast-feeding;
  19. Is receiving concurrent investigational therapy or has received investigational therapy within a period of 30 days prior to the first scheduled day of dosing (investigational therapy is defined as treatment for which there is currently no regulatory-authority-approved indication);
  20. Has previously received an organ or progenitor/stem cell transplant.

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:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:1
Imprime PGG + bevacizumab + paclitaxel/carboplatin
4 mg/kg, i.v. over 2 hr, weekly until progression or discontinuation
15 mg/kg, i.v., over 90 minutes, on Day 1 only of each 3-week treatment cycle
200 mg/m2, i.v. over 3 hr, on Day 2 of each 3-week treatment cycle for the first 4 to 6 treatment cycles.
AUC of 6 mg./mL · min based on the Calvert formula; i.v. over 30 min, on Day 2 of each 3-week treatment cycle for the first 4 to 6 treatment cycles
其他:2
bevacizumab + paclitaxel/carboplatin
15 mg/kg, i.v., over 90 minutes, on Day 1 only of each 3-week treatment cycle
200 mg/m2, i.v. over 3 hr, on Day 2 of each 3-week treatment cycle for the first 4 to 6 treatment cycles.
AUC of 6 mg./mL · min based on the Calvert formula; i.v. over 30 min, on Day 2 of each 3-week treatment cycle for the first 4 to 6 treatment cycles

研究衡量的是什么?

主要结果指标

结果测量
大体时间
To determine the objective response rate (ORR) in each study arm
大体时间:Approximately 1.5 years
Approximately 1.5 years

次要结果测量

结果测量
大体时间
To determine the disease control rate (DCR) in each study arm
大体时间:Approximately 1.5 years
Approximately 1.5 years
To determine the complete response (CR), partial response (PR), and stable disease (SD) rates in each study arm
大体时间:Approximately 1.5 years
Approximately 1.5 years
To determine the duration of objective tumor response in each study arm
大体时间:Approximately 1.5 years
Approximately 1.5 years
To determine the duration of stable disease in each study arm
大体时间:Approximately 1.5 years
Approximately 1.5 years
To determine the duration of time to progression (TTP) in each study arm
大体时间:Approximately 1.5 years
Approximately 1.5 years
To assess the safety of the dosing regimen within each study arm
大体时间:Approximately 1.5 years
Approximately 1.5 years
To determine the pharmacokinetic (PK) profile of Imprime PGG (in active treatment arm only)
大体时间:Approximately 1.5 years
Approximately 1.5 years

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。

调查人员

  • 首席研究员:Folker Schneller, MD、Klinikum Rechts der Isar der Technischen Universitaet Muenchen

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

2009年6月1日

初级完成 (实际的)

2016年4月1日

研究完成 (实际的)

2016年5月1日

研究注册日期

首次提交

2009年4月1日

首先提交符合 QC 标准的

2009年4月1日

首次发布 (估计)

2009年4月2日

研究记录更新

最后更新发布 (实际的)

2017年3月3日

上次提交的符合 QC 标准的更新

2017年3月1日

最后验证

2017年3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.

Imprime PGG® Injection的临床试验

3
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