EUCTR2005-003275-20-IT进行中（未招募）不适用
A Phase 3 Randomized, Open-Label Study of Docetaxel in Combination with CG1940 and CG8711 versus Docetaxel and Prednisone in Taxane-Naïve Patients with Metastatic Hormone-Refractory Prostate Cancer With Pain
Cell Genesys Ltd0 个研究点目标入组 600 人开始时间: 2006年8月3日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 600
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
- •Confirmed diagnosis of or clinical history consistent with adenocarcinoma of the prostate Males greater than 18 years of age Patients taking any Level 3 pain medication at any dose with any frequency. Patients taking Level 2 pain medication for cancer related pain, confirmed by investigator assessment. In order to assess the source of pain and the pain medication level (see Appendix E), the investigator should review the patient s completed assessment(s) of pain, perform a complete medical history, including current medications and physical examination, and review results from bone and CT scans. Metastatic prostate cancer deemed to be unresponsive or refractory to hormone therapy (after discontinuation of anti-androgen therapy) as determined by one of the following: Progressive measurable disease on CT scan or MRI as assessed using un-modified RECIST guidelines. Progressive non-measurable disease as defined by the appearance of one or more new lesions on bone scan. PSA progression, as defined by two consecutive rising PSA values obtained at least 2 weeks apart, and both obtained at least 4 weeks after discontinuation of any other antiandrogen therapy. The second PSA value must be 5.0 ng/mL Detectable metastases by bone scan, CT scan or MRI. Testosterone < 50 ng/dL (1.73 nmol/L). Must have had orchiectomy or is currently receiving an LHRH agonist/antagonist WBC > 3,000 cells/mm3, ANC > 1,500 cells/mm3, hemoglobin > 9 g/dL (5.6 mmol/L), and platelets > 100,000 cells/mm3 Serum creatinine < 2.0 mg/dL (177 µmol/L) Total or direct bilirubin < the upper limit of normal AST or ALT 1.5 times the upper limit of normal concomitant with alkaline phosphatase 2.5 times the upper limit of normal CD4+ lymphocytes > 200 cells/mm3 ECOG performance status 2 (performance status of 3 is allowed if due to bone pain) Life expectancy of at least 6 months If sexually active, willing to use barrier contraception during study drug treatment The ability to understand and the willingness to sign a written informed consent
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Transitional cell, small cell, neuroendocrine, or squamous cell prostate cancer Clinical evidence of brain metastases or history of brain metastases Third space fluid accumulation, such as ascites or symptomatic pleural effusion Clinically significant active infection or uncontrolled medical condition considered high-risk for docetaxel, corticosteroids or investigational new drug treatment Prior gene therapy or cancer vaccine for prostate cancer More than one prior systemic chemotherapy regimen, or any taxane chemotherapy. Patients must have completed chemotherapy at least 4 weeks prior to randomization and have recovered from all side effects.
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