EUCTR2017-000699-27-NL进行中(未招募)1 期
Repeated Rhenium-188-HEDP versus Radium-223-chloride in patients with metastatic castration-resistant prostate cancer; the RARE trial - RaRe
VU University Medical Center0 个研究点目标入组 402 人开始时间: 2018年2月22日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 402
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Male
入选标准
- •Male, 18 years and older.
- •Histologically confirmed prostate cancer
- •Bone metastases (=6 lesions) showing pathological uptake at bone scintigraphy
- •WHO performance status of =2.
- •Life expectancy of at least 6 months.
- •Castration-resistant disease: serum testosterone level of =1.7 nmol per liter (=50 ng per deciliter) after bilateral orchiectomy or during maintenance treatment consisting of androgen-ablation therapy with a luteinizing hormone-releasing hormone agonist. During study treatment the maintenance androgen-deprivation therapy must be continued.
- •Baseline PSA =5 ng/ml with evidence of progressively increasing PSA values (two consecutive increases over the previous reference value with at least a 1-week interval).
- •Symptomatic disease with either regular use of analgesic medication or treatment with external-beam radiotherapy for cancer-related bone pain within the previous 12 weeks.
- •Progression on or after treatment with docetaxel, or inability to receive docetaxel.
- •Adequate renal function (serum creatinine level =1.5 x ULN)
- •Adequate hematological function defined as absolute neutrophil count =1.5 x 109/L and platelet count =100 x 109/L, hemoglobin =6.0 mmol/L
- •Written informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 150
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 252
排除标准
- •Treatment with chemotherapy within the previous 4 weeks
- •Previous hemibody external radiotherapy.
- •Systemic radiotherapy with radioisotopes within the previous 24 weeks.
- •Malignant lymphadenopathy =3cm in the short-axis diameter.
- •Presence of visceral metastases.
- •Imminent or established spinal cord compression.
- •Active uncontrolled bacterial, viral or fungal infection.
- •History of another malignancy within the last five years except adequately treated basal cell carcinoma of the skin.
- •Organ allografts requiring immunosuppressive therapy
- •Any serious uncontrolled concomitant disease.
- •Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial.
研究者
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