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Study of AMG 386 in Combination With Paclitaxel and Carboplatin in Subjects With Ovarian Cancer

2015年10月13日 更新者:Amgen

A Phase 1b Open-Label, Multi-Center Study of AMG 386 in Combination With Paclitaxel and Carboplatin in Subjects With High-Risk Stage I and Stages II-IV Epithelial Ovarian, Primary Peritoneal or Fallopian Tube Cancers

To evaluate whether AMG 386 in combination with paclitaxel and carboplatin is safe and well tolerated in the first-line treatment of high-risk stage I and stages II-IV epithelial ovarian, primary peritoneal and fallopian tube cancers. The hypothesis is that AMG 386 in combination with carboplatin and paclitaxel is safe and well tolerated.

研究概览

详细说明

To evaluate whether AMG 386 in combination with paclitaxel and carboplatin is safe and well tolerated in the first-line treatment of high-risk stage I and stages II-IV epithelial ovarian, primary peritoneal and fallopian tube cancers. The hypothesis is that AMG 386 in combination with carboplatin and paclitaxel is safe and well tolerated.

研究类型

介入性

注册 (实际的)

27

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

      • Brussels、比利时、1000
        • Research Site
      • Bruxelles、比利时、1200
        • Research Site
      • Leuven、比利时、3000
        • Research Site
    • Victoria
      • Footscray、Victoria、澳大利亚、3011
        • Research Site
      • Malvern、Victoria、澳大利亚、3144
        • Research Site
      • Parkville、Victoria、澳大利亚、3052
        • Research Site
      • Madrid、西班牙、28040
        • Research Site
    • Cataluña
      • Barcelona、Cataluña、西班牙、08035
        • Research 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

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

女性

描述

Inclusion Criteria:

  • Female subjects more than 18 years of age with newly diagnosed high-risk FIGO Stage I (grade 3, or aneuploid grade 1 or 2) or Stages II-IV epithelial ovarian, primary peritoneal and fallopian tube cancer with an indication for first-line treatment with paclitaxel and carboplatin x 6 cycles. Subjects with pseudomyxoma, mesothelioma, adenocarcinoma of unknown primary tumor, sarcoma, or neuroendocrine histology are excluded.
  • Subjects with high-risk stage I, stage II, or stage IIIA-B must have had prior primary debulking surgery that occurred no less than 4 weeks, and no more than 12 weeks, prior to enrollment. Subjects must have recovered fully from surgery in the opinion of the investigator
  • Subjects with Stage IIIC or IV disease who have not had primary debulking surgery must have planned interval debulking surgery following 3 cycles of AMG 386, paclitaxel and carboplatin
  • Female 18 years of age or older at the time the written informed consent is obtained
  • Subjects of child-bearing potential who have not undergone a bilateral salpingo-oophorectomy and are sexually active must consent to use an accepted and effective non-hormonal method of contraception (i.e, double barrier method (eg, condom plus diaphragm) from signing the informed consent through 6 months after last dose of study drug
  • GOG Performance Status of 0 or 1
  • Life expectancy ≥ 3 months (per investigator opinion)
  • Subject plans to begin protocol-directed therapy within 7 days from enrollment
  • Adequate organ and hematological function as evidenced by the following laboratory studies prior to enrollment:

Hematological function, as follows:

  • Hemoglobin ≥ 9 g/dL
  • Absolute neutrophil count (ANC) ≥ 1.5 x 10x9/L
  • Platelet count ≥ 100 x 10x9/L and ≤ 850 x 10x9/L
  • PTT or aPTT ≤ 1.5 x ULN per institutional laboratory range and INR ≤ 1.5

Renal function, as follows:

  • Urinary protein quantitative value of ≤ 30 mg/dL in urinalysis or ≤ 1+ on dipstick, unless quantitative protein is < 1000 mg in a 24 hour urine sample
  • Creatinine clearance > 40 mL/min per 24-hr urine collection or calculated according to the Cockcroft-Gault formula

Hepatic function, as follows:

  • AST and ALT ≤ 2.5 x ULN per institutional laboratory range (or ≤ 5 x ULN if liver metastases are present)
  • Total bilirubin ≤ 1.5x institutions' ULN Nutritional
  • Albumin ≥ 2.8 g/dL

Exclusion Criteria:

  • Prior use of anticancer therapy or experimental therapy for epithelial ovarian, primary peritoneal or fallopian tube cancers
  • Previous abdominal and/or pelvic external beam radiotherapy
  • Subjects believed to be a higher than average risk of bowel perforation. This includes current symptoms of partial or complete bowel obstruction, recent (within 6 months) history of fistula or bowel perforation, subjects requiring total parenteral nutrition and continuous hydration
  • History of arterial or venous thromboembolism within 12 months prior to enrollment
  • History of clinically significant bleeding within 6 months prior to enrollment
  • History of central nervous system metastasis
  • Known active or ongoing infection (except uncomplicated urinary tract infection) within 14 days prior to enrollment
  • Currently or previously treated with AMG 386, or other molecules that inhibit the angiopoietins or Tie2 receptor
  • Current or within 30 days prior to enrollment treatment with immune modulators such as systemic cyclosporine or tacrolimus
  • Prior myeloablative high-dose chemotherapy with allogeneic or autologous stem cell (or bone marrow) transplant
  • Clinically significant cardiac disease within 12 months prior to enrollment, including myocardial infarction, unstable angina, grade 2 or greater peripheral vascular disease, cerebrovascular accident, transient ischemic attack, congestive heart failure, or arrhythmias not controlled by outpatient medication or placement of percutaneous transluminal coronary angioplasty/stent
  • Uncontrolled hypertension as defined as diastolic blood pressure > 90 mmHg OR systolic blood pressure > 140 mmHg. The use of anti-hypertensive medications to control hypertension is permitted
  • Subjects with a history of prior malignancy, except:

Malignancy treated with curative intent and with no known active disease present for ≥ 3 years prior to enrollment and felt to be at low risk for recurrence by treating physician, Adequately treated non-melanomatous skin cancer or lentigo maligna without evidence of disease Adequately treated cervical carcinoma in situ without evidence of disease

  • Major surgery within 28 days prior to enrollment or still recovering from prior surgery
  • Minor surgical procedures, including placement of tunneled central venous access device, within 3 days prior to enrollment
  • History of allergic reactions to bacterially-produced proteins
  • Hypersensitivity to paclitaxel or drugs using the vehicle cremophor
  • Pregnant (ie, positive beta-human chorionic gonadotropin test) or is breast feeding or planning to become pregnant within 6 months after the end of treatment
  • Subject has known positive test(s) for human immunodeficiency virus (HIV) infection, hepatitis C virus, acute or chronic active hepatitis B infection
  • Any condition which in the investigator's opinion makes the subject unsuitable for study participation
  • Any uncontrolled concurrent illness or history of any medical condition that may interfere with the interpretation of the study results
  • Non-healing wound, ulcer (including gastrointestinal) or fracture
  • Subject has previously been enrolled onto this study
  • Subject will not be available for follow-up assessment
  • Subject has known sensitivity to any of the products to be administered during dosing
  • Subject has any kind of disorder that compromises the ability of the subject to give written informed consent and/or to comply with study procedures

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:AMG 386, paclitaxel and carboplatin
15 mg/Kg AMG 386 IV (intravenous) weekly plus paclitaxel and carboplatin IV Q3W for 18 weeks, followed by 15mg/Kg AMG 386 IV (intravenous) weekly alone for an additional 18 months.
15 mg/Kg AMG 386 IV (intravenous) weekly plus paclitaxel and carboplatin IV Q3W for 18 weeks, followed by 15mg/Kg AMG 386 IV (intravenous) weekly alone for an additional 18 months.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
To evaluate whether AMG 386 in combination with paclitaxel and carboplatin is safe and well tolerated in the first-line treatment of high-risk stage I and stages II-IV epithelial ovarian, primary peritoneal and fallopian tube cancers.
大体时间:18 weeks of combination therapy
18 weeks of combination therapy

次要结果测量

结果测量
大体时间
To evaluate the pharmacokinetics (Cmax, AUC and Cmin) of AMG 386 in combination with carboplatin and paclitaxel
大体时间:Week 1 until Week 7
Week 1 until Week 7
To estimate the incidence of anti-AMG 386 antibody formation
大体时间:Week 1 until maximum of 1 year following first dose
Week 1 until maximum of 1 year following first dose
To evaluate the objective response rate (ORR) among subjects receiving AMG 386 in combination with carboplatin and paclitaxel
大体时间:From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
To evaluate the duration of response (DOR) among subjects receiving AMG 386 in combination with carboplatin and paclitaxel
大体时间:From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
To evaluate progression-free survival (PFS) among subjects receiving AMG 386 in combination with carboplatin and paclitaxel
大体时间:From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
To evaluate the number of participants with adverse events and clinical laboratory abnormalities
大体时间:96 weeks
96 weeks
To evaluate the effect of AMG 386 on the pharmacokinetics (Cmax, AUC and Cmin) of carboplatin and paclitaxel
大体时间:Week 1 until Week 7
Week 1 until Week 7

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。

赞助

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

2010年11月1日

初级完成 (实际的)

2012年10月1日

研究完成 (实际的)

2015年1月1日

研究注册日期

首次提交

2010年10月21日

首先提交符合 QC 标准的

2010年12月2日

首次发布 (估计)

2010年12月3日

研究记录更新

最后更新发布 (估计)

2015年10月14日

上次提交的符合 QC 标准的更新

2015年10月13日

最后验证

2015年10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.

AMG 386, paclitaxel and carboplatin的临床试验

3
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