JPRN-UMIN000030946招募中未知
Efficacy and Safety of Ra-223 as 1st line therapy in combination with alternative anti-androgen therapy for bone metastatic CRPC Patients - 1st Ra-223 Therapy Trial
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 30
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
- 20years-old 至 ot applicable（—）
- 性别
- Male
入选标准
- 未提供
排除标准
- •1) Treatment history of cytotoxic chemotherapy (including Estramustine 2) Prior hemibody external radiation therapy 3) Systemic radiation therapy with radioisotopes (storontium-89, samarium-153, rhenium-186, or rhenium-188) within previous 24 weeks 4) Prior treatment of Ra-223 5) Blood transfusion or erythropoietin-stimulating agents within the previous 4 weeks 6) Other malignancy treated within the last 5 years (except non-melanoma skin cancer or low-grade superficial bladder cancer) 7) History or presence of visceral metastases or brain metastases 8) Malignant lymphadenopathy exceeding 3 cm in short-axis diameter 9) Imminent or established spinal cord compression. Patients with history of spinal cord compression must have completely recovered 10) Presence of liver disorders 11) Any other serious illness or medical condition such as, but not limited to; any uncontrolled infection; cardiac failure NYHA III or IV; Crohn's disease or Ulcerative colitis; Bone marrow dysplasia 12)Unmanageable faecal incontinence 13) Patients who are inappropriate for the participation into this study due to any other reasons judged by each institutional physician
研究者
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