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临床试验/NCT00172068
NCT00172068终止2 期

Efficacy and Tolerability of Intravenous Zometa® (Zoledronic Acid) 4 mg in Primary Breast Cancer Patients With Disseminated Tumor Cells in Bone Marrow. A Prospective, Randomized, Parallel Group, Open-label, Clinical Pilot Study.

Novartis Pharmaceuticals2 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2002年1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
终止
入组人数
96
试验地点
2
主要终点
Reduction of detected tumor cells in bone marrow

研究概览

简要总结

Metastatic bone disease is an important prognostic factor for survival which will in median be close to two years after first diagnosis of osseous metastases. This open-label study will investigate the safety and efficacy of zoledronic acid in patients with breast cancer and minimal residual disease in the bone marrow.

研究设计

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

入排标准

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

入选标准

  • Patients, with primary breast cancer who had undergone complete primary tumor resection and axillary lymph node dissection
  • Evidence of minimal residual disease (disseminated tumor cells in bone marrow)
  • Patients had to receive one of the following adjuvant therapy categories: chemotherapy ± hormonal therapy or hormonal therapy alone

排除标准

  • Inflammatory, metastatic or recurrent breast cancer or a history of breast cancer prior to the currently diagnosed case
  • Neo-adjuvant chemotherapy, neo-adjuvant hormonal therapy, or neo-adjuvant radiotherapy
  • Prior stem cell rescue/bone marrow transplant
  • History of other cancers aside from non-melanomatous skin cancer or carcinoma in situ of the uterine cervix
  • Additional protocol-defined inclusion / exclusion criteria may apply

研究组 & 干预措施

Treatment Group

Experimental

干预措施: Zoledronic acid + Calcium/Vitamin D (Drug)

Control Group

Active Comparator

干预措施: Zoledronic acid + Calcium/Vitamin D (Drug)

结局指标

主要结局

Reduction of detected tumor cells in bone marrow

时间窗: 12 months

次要结局

  • Tumor cell detection in bone marrow in comparison to the time point of primary surgery (Baseline).(24 months)
  • Bone metastases-free survival(24 months)
  • Disease-free survival(24 months)
  • Bone mineral density(at 12 and 24 months)
  • Number and localization of bone metastases(24 months)

研究者

申办方类型
Industry

研究点 (2)

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