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临床试验/NCT01065246
NCT01065246已完成2 期

Phase II Open Label Study to Evaluate the Safety of a Second I.P. Infusion Cycle of Catumaxomab in Patients With Malignant Ascites Due to Carcinoma, Requiring Their First Therapeutic Puncture After Treatment in the CASIMAS Study

Neovii Biotech1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2009年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
8
试验地点
1
主要终点
proportion of patients who are able to receive a second cycle of catumaxomab

研究概览

简要总结

This phase II single arm, open-label study investigate the safety of a second cycle of catumaxomab in patients with malignant ascites due to carcinoma, requiring their first therapeutic puncture after treatment in the CASIMAS study.

详细描述

Up to 30 evaluable patients from the CASIMAS study will be enrolled. Catumaxomab will be infused intraperitoneally with 3hour constant-rate infusions 4 times within 11 days with ascending dosages (10 - 20 - 50 - 150 µg).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients who have completed 4 infusions of catumaxomab in the CASIMAS study
  • age >= 18 years
  • Karnofsky index >= 60 %
  • patients with malignant ascites requiring their first therapeutic ascites paracentesis after at least 60days following last catumaxomab infusion in the CASIMAS study
  • Patients where standard therapy is either not available or no longer feasible

排除标准

  • acute or chronic infection
  • concomitant treatment with investigational products other than catumaxomab, cancer, chemo- or radiotherapy
  • previous treatment with entirely murine monoclonal antibodies other than catumaxomab
  • liver metastases with volume >70 % of liver metastasized tissue

研究组 & 干预措施

catumaxomab

Experimental

干预措施: catumaxomab (Drug)

结局指标

主要结局

proportion of patients who are able to receive a second cycle of catumaxomab

时间窗: 1 month

次要结局

  • puncture free survival(1-3 months)
  • incidence and severity of adverse events(1 month)
  • Quality of Life(1 month)
  • Development of human-anti-mouse antibodies(1 month)

研究者

发起方
Neovii Biotech
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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