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Intratumoral Application of L19IL2 in Patients With Malignant Melanoma

2014年11月19日 更新者:Philogen S.p.A.

A Phase II Study of Intratumoral Application of L19IL2 in Patients With Stage III/IV Melanoma.

Phase II, non-randomized, multicenter, prospective study designed to test the efficacy and safety of intratumorally administered L19IL2 in patients suffering from metastatic melanoma.

研究概览

详细说明

Phase II, non-randomized, multicenter, prospective study designed to test the efficacy and safety of intratumorally administered L19IL2. L19IL2 binds with high affinity to the EDB domain of Fibronectin, a marker of angiogenesis which is strongly upregulated in malignant melanoma lesions. This binding leads to an increased residence time of the protein at the site of disease. The biologic effect of the IL2 moiety is identical to the one of free IL-2.

The study treatment is up to 20 MioIU L19IL2 per week in patients suffering from histopathologically-proven malignant melanoma with presence of injectable soft-tissue metastases either in clinical stage III or stage IV M1a without visceral metastases. The duration of treatment could be up to 20 weeks. After the end of study visit follow-up is performed every 6 weeks until 12 months from enrollment of each patient.

Tumor assessment will be performed within 2 weeks before start of treatment and at week 12 using immune-related response criteria and RECIST 1.1. To assure that patients do not develop visceral metastases under treatment, an additional tumor assessment will be performed already at week 6 after start of therapy. Assessments at week 24 and 36 will be performed according to RECIST vs. 1.1 criteria only.

Treatment emergent adverse events will be summarized by Common Toxicity Criteria (version 4.02, CTCAE) and worst grade for all treated patients. Laboratory values and change in vital signs will be summarized.

研究类型

介入性

注册 (实际的)

25

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

      • Graz、奥地利
        • Universitätsklinik Graz
      • Hannover、德国
        • Medizinischen Hochschule Hannover
      • Tuebingen、德国
        • University Hospital

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:

  • Histopathologically proven malignant melanoma.
  • Presence of measurable and injectable soft tissue metastases either in clinical stage III or stage IV M1a.
  • Males or females, age >/= 18 years.
  • Either without, or after one line of prior systemic treatment for metastatic disease.
  • ECOG performance status < 2.
  • LDH < 2 x the upper limit of normal.
  • Life expectancy of at least 12 weeks.
  • Absolute neutrophil count > 1.5 x 10^9/L.
  • Hemoglobin > 9.0 g/dL.
  • Platelets > 100 x 10^9/L.
  • Total bilirubin ≤ 30 µmol/L (or ≤ 2.0 mg/dl).
  • ALT and AST ≤ 2.5 x the upper limit of normal (ULN) (5.0 x ULN for patients with hepatic involvement with tumor).
  • Serum creatinine < 1.5 x ULN.
  • All acute toxic effects (excluding alopecia) of any prior therapy must have resolved to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) (v4.02) Grade ≤ 1 unless otherwise specified above.
  • Negative serum pregnancy test (for women of child-bearing potential only) at screening.
  • If of childbearing potential, agreement to use adequate contraceptive methods (e.g., oral contraceptives, condoms, or other adequate barrier controls, intrauterine contraceptive devices, or sterilization) beginning at the screening visit and continuing until 3 months following last treatment with study drug.
  • Able to provide written Informed Consent.
  • Willingness and ability to comply with the scheduled visits, treatment plan, laboratory tests and other study procedures.

Exclusion Criteria:

  • Primary ocular melanoma.
  • Presence of visceral metastases at screening.
  • Evidence of active brain metastases at screening.
  • Previous or concurrent cancer that is distinct in primary site or histology from the cancer being evaluated in this study except cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors (TA, Tis & Ti) or any cancer curatively treated < 5 years prior to study entry.
  • History of HIV infection or infectious hepatitis B or C.
  • Presence of active infections (e.g. requiring antimicrobial therapy) or other severe concurrent disease, which, in the opinion of the investigator, would place the patient at undue risk or interfere with the study.
  • History within the last year of acute or subacute coronary syndromes including myocardial infarction, unstable or severe stable angina pectoris.
  • Inadequately controlled cardiac arrhythmias including atrial fibrillation.
  • Heart insufficiency (> Grade II, New York Heart Association (NYHA) criteria).
  • Uncontrolled hypertension.
  • Ischemic peripheral vascular disease (Grade IIb-IV).
  • Severe diabetic retinopathy.
  • Active autoimmune disease.
  • History of organ allograft or stem cell transplantation.
  • Recovery from major trauma including surgery within 4 weeks prior to administration of study treatment.
  • Known history of allergy to IL2, or other intravenously administered human proteins/peptides/antibodies.
  • Breast feeding female.
  • Anti-tumor therapy within 4 weeks of the administration of study treatment (except small surgery).
  • Previous in vivo exposure to monoclonal antibodies for biological therapy in the 6 weeks before administration of study treatment.
  • Planned administration of growth factors or immunomodulatory agents within 7 days before the administration of study treatment.
  • Patients in need of systemic treatment for rapidly progressive systemic disease during study treatment and up to 2 weeks after injection of L19IL2.
  • Patient requires, or is taking, corticosteroids or other immunosuppressant drugs on a long-term basis. Limited use of corticosteroids to treat or prevent acute hypersensitivity reactions is not considered an exclusion criterion.
  • Any condition, that in the opinion of the investigator could hamper compliance with the study protocol.

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:L19IL2
Patients will be treated with intratumoral injections of L19IL2 1-3 x weekly. The maximum cumulative dose per week is 20 MioIU. Treatment duration is up to 20 weeks.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Rate of patients with complete response (CR) of L19IL2 treated Index/Non-Index lesions at week 12 .
大体时间:week 12
week 12

次要结果测量

结果测量
大体时间
总生存期(OS)
大体时间:1年
1年
Safety of intratumoral administration of L19IL2
大体时间:1-29 days
1-29 days
Rate of patients with complete response (CR), partial response (PR) and stable disease (SD) of L19IL2 treated Index/Non-Index lesions at week 12.
大体时间:week 12
week 12
Duration of objective response and disease control of L19IL2 treated Index/Non-Index lesions
大体时间:week 6-46
week 6-46
Rate of patients with complete response (CR), partial response (PR) and stable disease (SD)of all metastases
大体时间:week 12
week 12
Objective response rate of all metastases
大体时间:week 24, week 36
week 24, week 36
Disease control rate of all metastases
大体时间:week 24, week 36
week 24, week 36

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

2010年4月1日

初级完成 (实际的)

2013年9月1日

研究完成 (实际的)

2013年9月1日

研究注册日期

首次提交

2010年12月2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)

2014年11月20日

上次提交的符合 QC 标准的更新

2014年11月19日

最后验证

2014年11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.

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