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临床试验/NCT00219219
NCT00219219已完成4 期

Zoledronic Acid in the Prevention of Skeletal-related Events in Hormone Refractory and Hormone-sensitive Prostate Cancer Patients With Bone Metastases

Novartis1 个研究点 分布在 1 个国家开始时间: 2003年9月1日最近更新:
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相关药物

试验速览

阶段
4 期
状态
已完成
发起方
Novartis
试验地点
1
主要终点
occurence of skeletale related events (SREs) over time (time to first SRE,skeletal morbidity rate and proportion of patients experiencing SRE)

研究概览

简要总结

The present study will give information about the course over time in skeletal-related events (SRE) in prostate cancer patients with bone metastases treated with zoledronic acid 4 mg administered as a 15-minute infusion every 4 weeks for a maximum of 15 infusions. The protocol will enroll patients with recent diagnosis of bone metastases from prostate cancer who are hormone-refractory, hormone-naïve or still hormone-sensitive, that represent the entire population of prostate cancer patients

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
Male
接受健康志愿者

入选标准

  • Patients aged ≥18 years
  • Written informed consent
  • Histologically-proven prostate carcinoma
  • ECOG performance status ≤ 2
  • Life expectancy > 6 months
  • Newly diagnosed (≤ 6 months prior to visit 1) bone metastases evidenced by bone scan or radiograph.
  • Patients on androgen deprivation therapy (medical therapy with LHRH analogues + antiandrogens or surgical castration) or going to start it
  • Patients with partners of childbearing potential should use a barrier method of contraception throughout the study

排除标准

  • Patients without a history of metastatic disease to the bone
  • Prior treatment with bisphosphonates
  • SREs prior to visit 2
  • Prior treatment with calcitonin, mithramycin, or gallium nitrate within 2 weeks prior to baseline
  • Corrected (adjusted for serum albumin - see Appendix 5 for the calculation) serum calcium concentration < 8.0 mg/dl (2.00 mmol/l)
  • Serum creatinine concentration > 265 micromol/l (3.0 mg/dl) or a calculated creatinine clearance < 30 ml/minute or serious underlying renal disease or prior renal transplantation
  • History of other malignant neoplasm within previous five years with exception of non-melanomatous skin cancer which has been satisfactorily treated
  • Other known concurrent, severe medical disorder jeopardizing the life of the patient in the immediate future
  • Patients treated with systemic investigational drug(s) and/or device(s) within the past 30 days or topical investigational drugs within the past 7 days
  • Known hypersensitivity to zoledronic acid or other bisphosphonates
  • History of noncompliance to medical regimens and patients who are considered potentially unreliable (for example drug or alchohol abusers) or incapable of giving informed consent as judged by the investigator

结局指标

主要结局

occurence of skeletale related events (SREs) over time (time to first SRE,skeletal morbidity rate and proportion of patients experiencing SRE)

次要结局

  • Bone pain
  • Use of analgesic medication and ECOG performance status every three months
  • Bone specific alkaline phosphatase, serum N-telopeptide and parathyroid hormone will be evaluated after one month of treatment and then every three months

研究者

发起方
Novartis
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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