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临床试验/NCT01612286
NCT01612286Unknown2 期

A Phase II Clinical Study of Endostar Combination With Chemotherapy in the Metastatic Nasopharyngeal Carcinoma

Zhejiang Cancer Hospital1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2012年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
30
试验地点
1
主要终点
progress free survival(PFS)

研究概览

简要总结

The investigators designed this study to evaluate the efficiency and the acute toxicities of recombinant human endostatin (endostar) combined with chemotherapy in the metastatic nasopharyngeal carcinoma (NPC).

详细描述

To evaluate the progression free survival (PFS), overall survival (OS), Acute adverse reaction of recombinant human endostatin (endostar) combined with chemotherapy to the metastatic nasopharyngeal carcinoma (NPC).

研究设计

研究类型
Interventional
分配方式
Na
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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed metastatic NPC patient who have received radiotherapy or chemoradiotherapy with an at least 6 months interval
  • Have measurable lesions
  • No dysfunction of the major organs
  • Can understand this study and give a signed informed consent certificates
  • without a history of allergic reaction to the biological agents

排除标准

  • Pregnant or lactating women; Women of child-bearing age without contraception
  • with a Serious infection or dysfunction of the major organs
  • have taken other antitumor drugs during the period of 30 days ahead of this clinical trial
  • allergic to the Escherichia coli preparations
  • Cann't understand this study and give a signed informed consent certificates

研究组 & 干预措施

endostatin

Experimental

chemotherapy concurrently with endostatin

干预措施: endostatin (Drug)

结局指标

主要结局

progress free survival(PFS)

时间窗: 1 year and 2years

PFS means assignament to the date of any local or distant progress of the disease useing Kaplan-Meier caculate the progress free survival rates

次要结局

  • overall survival(OS)(baseline to date of death from any cause)
  • Adverse events(participants will be followed for the duration of hospital stay,an expected average of 100 days and every 3 months thereafter for 1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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