EUCTR2012-000075-16-IT进行中（未招募）不适用
Radium-223 Chloride (Alpharadin) in Castration-Resistant (Hormone- Refractory) Prostate Cancer Patients with Bone Metastasis
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 1,925
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
- •- Has provided written informed consent. Subjects must be able to understand and be willing to sign the written informed consent form (ICF). A signed ICF must be appropriately obtained prior to the conduct of the any trial- specific procedure. • Age = 18 years • Histologically or cytologically confirmed prostate cancer • Patients diagnosed with progressive bone predominant metastatic CRPC/HRPC with at least two skeletal metastases on bone scan with no lung, liver, and/or brain metastasis (lymph node only metastasis is allowed) • Progressive disease is defined either by: - The appearance of new bone lesions. If progression is based on new lesion(s) on bone scan only without an increase in PSA, PSA values from 3 assessments within the last 6 months must be provided; OR - In the absence of a new bone lesions by 2 consecutive increases in serum PSA over previous reference value, which should not be more than 6 months before screening, each measured at least 1 week apart with the last PSA =5 ng/mL • Life expectancy = 6 months • ECOG PS 0-2 • Adequate hematological, liver and renal function o Absolute neutrophil count (ANC) = 1.5 x109/L o Platelet count = 100 x109/L o Hemoglobin =10.0 g/dL (100 g/L; 6.2 mmol/L) o Total bilirubin level = 1.5 x institutional upper limit of normal (ULN) o Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) = 2.5 x ULN o Creatinine = 1.5 x ULN o Albumin > 25 g/L • Willing and able to comply with the protocol, including follow-up visits and examinations
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 925
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 1000
排除标准
- •Treatment with an investigational drug within previous 4 weeks, or planned during the treatment period or follow-up • Eligible for first course of docetaxel, i.e., patients who are fit enough, willing, and who are located where treatment with docetaxel is available • Treatment with cytotoxic chemotherapy within previous 4 weeks, or failure to recover from AEs due to cytotoxic chemotherapy administered more than 4 weeks previous (however, ongoing neuropathy is permitted) • Received previous radiotherapy to approximately > 25% of bone marrow, including hemibody radiation • Received systemic therapy with radionuclides (e.g., strontium-89, samarium-153, rhenium-186, or rhenium-188, or radium-223 chloride) for the treatment of bony metastases • Other malignancy treated within the last 3 years (except nonmelanoma skin cancer or low-grade superficial bladder cancer) • Visceral metastases as assessed by abdominal or pelvic computed tomography (CT) or other imaging modality • Presence of brain metastases • Lymphadenopathy exceeding 6 cm in short-axis diameter • Any size pelvic lymphadenopathy if it is thought to be a contributor to concurrent hydronephrosis. • Imminent or history of spinal cord compression based on clinical findings and/or magnetic resonance imaging (MRI) • Any other serious illness or medical condition, such as but not limited to: o Any infection = NCI-CTCAE v.4.03 Grade 2 o Cardiac failure New York Heart Association (NYHA) III or IV o Crohn's disease or ulcerative colitis o Bone marrow dysplasia • Fecal incontinence
研究者
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