跳至主要内容
临床试验/CTRI/2010/091/001135
CTRI/2010/091/001135进行中(未招募)2 期

A Multi Centre, Pilot Phase II Trial Assessing The Efficacy And Safety Of Bevacizumab + Gemcitabine + Carboplatin As First Line Treatment For Patients Diagnosed With Triple Negative Metastatic Breast Cancer.

Roche Products India Pvt Ltd0 个研究点目标入组 44 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
进行中(未招募)
入组人数
44

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

入选标准

  • * Female patients, >/= 18 years of age
  • * Metastatic breast cancer
  • * Estrogen receptor- , progesterone- and HER2-negative disease
  • * Treatment-naïve for metastatic breast cancer
  • * Eastern Cooperative Oncology Group (ECOG) performance status 0-1
  • * Adequate hematological, renal and liver function

排除标准

  • Prior first line treatment for metastatic breast cancer
  • CNS metastasis
  • Uncontrolled hypertension ( 170/95 mmHg)
  • Evidence of bleeding diathesis, coagulopathy or hemorrhage at baseline
  • History of other malignant disease within past 3 years, except for curatively treated basal cell carcinoma of the skin and carcinoma in situ of the cervix
  • Prior therapy with gemcitabine or carboplatin in the metastatic setting. Patients having received gemcitabine or carboplatin as part of adjuvant therapy are eligible, if recurrence was first documented 6 months after the last exposure to the drug(s)
  • Requirement of chronic use of immunosuppressive agents
  • HIV, hepatitis B or hepatitis C infection

研究者

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