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临床试验/JPRN-jRCT2080222700
JPRN-jRCT2080222700未知2 期

A Phase II Trial of R435(Bevacizumab) in stage IVB, persistent or recurrent carcinoma of the cervix

Chugai Pharmaceutical Co., Ltd.0 个研究点目标入组 6 人开始时间: 2014年12月19日最近更新:
适应症

试验速览

阶段
2 期
入组人数
6

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
Female

入选标准

  • Adult patients, >=20 years of age.
  • - GOG Performance Status of 0 or 1.
  • - Primary stage IVB, persistent or recurrent carcinoma of the cervix which is not amenable to curative treatment.

排除标准

  • - Previously treated with chemotherapy except when used concurrently with radiation therapy.
  • - Serious non-healing wound, ulcer, or bone fracture. This includes history of abdominal fistula, gastrointestinal perforation or intra-abdominal abscess within 6 months must pass before study entry.
  • - History or evidence upon physical examination of CNS disease.
  • - History of hemoptysis(>=Grade2) within 1 month before study entry.

研究者

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