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Study of Immune Response Modifier in the Treatment of Breast, Ovarian, Endometrial and Cervical Cancers

Phase II Study of 852A Administered Subcutaneously in Patients With Metastatic Refractory Breast, Ovarian, Endometrial and Cervical Cancers

The purpose of this study is to evaluate the anti-tumor activity of 852A when used to treat metastatic breast, ovarian, endometrial or cervical cancer not responding to standard treatment.

研究概览

地位

完全的

干预/治疗

详细说明

852A will be administered as a subcutaneous injection (SC) 2 times per week for 12 weeks (24 doses) with provisions for dose escalation or reduction based on tolerability.

研究类型

介入性

注册 (实际的)

15

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

    • Minnesota
      • Minneapolis、Minnesota、美国、55455
        • Masonic Cancer Center, University of Minnesota

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:

  • Adequate performance status:

    • Breast - Karnofsky score > 50;
    • Ovarian, endometrial or cervical - Gynecologic Oncology Group (GOG) performance score ≤2
  • If female and of childbearing potential, are willing to use adequate contraception (hormonal, barrier method, abstinence) prior to study entry and for the duration of study participation.
  • Normal organ function within 14 days of study entry
  • Diagnosis of one of the following malignancies:

    • Metastatic breast cancer (BR)
    • Metastatic ovarian cancer (OV)
    • Metastatic endometrial cancer (EM)
    • Metastatic cervical cancer (CX)

Breast Cancer Inclusion Criteria:

  • Measurable metastatic disease (>1cm) in at least one site other than bone-only
  • Progression on or failure to respond to at least one previous chemotherapy regimen for metastatic disease
  • Progression on prior therapy with a hormonal agent if estrogen receptor or progesterone receptor positive, and/or with trastuzumab if HER2-neu positive. If patient has progressed through hormone or trastuzumab therapy only, must have received one chemotherapy regimen.

Ovarian Cancer Inclusion Criteria:

  • Measurable metastatic disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST)
  • Primary tumor must have been diagnosed histologically as either epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer (not borderline or low malignant potential epithelial carcinoma).
  • Subjects must have failed at least two previous chemotherapy regimens. Paclitaxel must have been a component of one or both regimens and cisplatin or carboplatin must have been a component of one or both regimens.

Endometrial Cancer Inclusion Criteria:

  • Measurable metastatic disease
  • Histologically proven recurrent or persistent endometrial cancer that is not amenable to curative treatment with surgery and/or radiation therapy AND has failed 2 previous treatment regimens

Cervical Cancer Inclusion Criteria:

  • Measurable metastatic disease
  • Histologically proven recurrent or persistent squamous cell carcinoma, adenosquamous carcinoma, or adenocarcinoma of the cervix that is not amenable to curative treatment with surgery and/or radiation therapy AND has failed 2 previous treatment regimens.

Exclusion Criteria:

  • Had/have the following prior/concurrent therapy:

    • Systemic corticosteroids (oral or injectable) within 7 days of first dose of 852A (topical or inhaled steroids are allowed)
    • Investigational drugs/agents within 14 days of first dose of 852A
    • Immunosuppressive therapy, including cytotoxic agents within 14 days of first dose of 852A (nitrosoureas within 30 days of first dose)
    • Drugs known to induce QT interval prolongation and/or induce Torsades de pointes unless best available drug required to treat life-threatening conditions
    • Radiotherapy within 3 weeks of the first dose of 852A
    • Hematopoietic cell transplantation within 4 weeks of first dose of 852A
    • Evidence of active infection within 3 days of first dose of 852A
    • Active fungal infection or pulmonary infiltrates (prior treated disease stable for 2 weeks is allowable)
    • Cardiac ischemia, cardiac arrhythmias or congestive heart failure uncontrolled by medication
    • History of, or clinical evidence of, a condition which, in the opinion of the investigator, could confound the results of the study or put the subject at undue risk
    • Uncontrolled intercurrent or chronic illness
    • Active autoimmune disease requiring immunosuppressive therapy within 30 days
    • Active coagulation disorder not controlled with medication
    • Pregnant or lactating
    • Concurrent malignancy (if in remission, at least 5 years disease free) except for localized (in-situ) disease, basal carcinomas and cutaneous squamous cell carcinomas that have been adequately treated
    • Any history of brain metastases or any other active central nervous system (CNS) disease

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: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:Intent-To-Treat
Patients treated with at least one dose - 852A subcutaneous injection.
0.2% 852a subcutaneous injection, 2 times per week for 12 weeks (24 doses) starting at 0.6 mg/m2; subsequent dose escalation for additional courses may be increased by 0.2 mg/m2 not to exceed 1.2 mg/m2.
其他名称:
  • TLR-7
  • Toll-like receptor-7
实验性的:Evaluable Cohort
Patients who received all 24 doses of 852A per protocol.
0.2% 852a subcutaneous injection, 2 times per week for 12 weeks (24 doses) starting at 0.6 mg/m2; subsequent dose escalation for additional courses may be increased by 0.2 mg/m2 not to exceed 1.2 mg/m2.
其他名称:
  • TLR-7
  • Toll-like receptor-7

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
Patients With Tumor Response (Response Evaluation Criteria in Solid Tumors) Who Received All 24 Doses of 852A.
大体时间:after 12 weeks (24 doses of 852A)
Assessment of anti-tumor activity of 852A using Response Evaluation Criteria in Solid Tumors (RECIST) criteria to evaluate tumor response after 24 doses. Complete Response (CR)= disappearance of all target lesions, Partial Response (PR) = at least 30% decrease in sum of longest diameter of target lesions, Progressive Disease (PD) = at least 25% increase in sum of longest diameter of target lesions, Stable Disease = neither PR or PD.
after 12 weeks (24 doses of 852A)

次要结果测量

结果测量
措施说明
大体时间
Mean Difference Values for Interleukin 1 Receptor Antagonist (IKL1ra)
大体时间:Prior to Dose 1 and 6 hours after Dose 1
Measures the difference of IL1ra (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
Prior to Dose 1 and 6 hours after Dose 1
Mean Difference Values for 10 kDa Interferon-gamma-induced Protein (IP-10)
大体时间:Prior to Dose 1 and 6 Hours Post-Dose
Measures differences in IP-10 (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
Prior to Dose 1 and 6 Hours Post-Dose
Mean Difference Values for Macrophage Inflammatory Protein-1 Alpha (MIP-1a)
大体时间:Prior to Dose 1 and 6 Hours Post-Dose
Measures difference in MIP-1a (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
Prior to Dose 1 and 6 Hours Post-Dose
Mean Difference Values for Macrophage Inflammatory Protein-1 Beta (MIP-1b)
大体时间:Prior to Dose 1 and 6 Hours Post-Dose
Measures difference in Macrophage Inflammatory Protein-1 Beta (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
Prior to Dose 1 and 6 Hours Post-Dose
Mean Difference Values for Soluble CD40 Ligand (sCD40L)
大体时间:Prior to Dose 1 and 6 Hours Post-Dose
Measures difference in Soluble CD40 ligand (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
Prior to Dose 1 and 6 Hours Post-Dose
Mean Difference Values for Tumor Necrosis Factor-alpha (TNF-a)
大体时间:Prior to Dose 1 and 6 Hours Post-Dose
Measures difference in Tumor necrosis factor-alpha (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
Prior to Dose 1 and 6 Hours Post-Dose

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。

合作者

调查人员

  • 首席研究员:Sarah Cooley, MD、Masonic Cancer Center, University of Minnesota

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

2006年4月1日

初级完成 (实际的)

2007年12月1日

研究完成 (实际的)

2008年12月1日

研究注册日期

首次提交

2006年4月27日

首先提交符合 QC 标准的

2006年4月27日

首次发布 (估计)

2006年4月27日

研究记录更新

最后更新发布 (实际的)

2019年8月26日

上次提交的符合 QC 标准的更新

2019年8月21日

最后验证

2019年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • 06US03IMP-852A
  • MT2006-02 (其他标识符:Blood and Bone Marrow Transplantation Program)
  • 2006LS005 (其他标识符:Masonic Cancer Center, University of Minnesota)

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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