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临床试验/NL-OMON30787
NL-OMON30787已完成不适用

The Prostate CARE Study: Capecitabine (Xeloda??) combined with Rhenium-188-HEDP in hormone refractory prostate cancer patients with bone metastases; a Capecitabine phase I dose escalation study and phase II efficacy study. - The Prostate CARE Study

Academisch Medisch Centrum0 个研究点目标入组 33 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
33

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
18 至 99(—)

入选标准

  • Histologically documented prostate cancer; presence of more than one osteoblastic bone metastases; hormone refractory disease; bone pain; life expectancy of at least 3 months; informed consent.

排除标准

  • Previous chemotherapy within 6 weeks prior to screening; prior treatment with systemic radiotherapeutic bone agent within a specified period; previous external beam radiotherapy within a specified period; active CNS or epidural brain metastases. ANC < 2 10^9/L; Platelet count < 150 10^9/L; Hb < 6 mmol/L; PSA > 5 microgram/L.

研究者

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