Study of DN101 and Taxotere in Patients With Advanced Non-Small Cell Lung Cancer
A Phase 1/2 Multicenter, Open Label, Dose Ranging Study of DN-101 and Taxotere® in Patients With Advanced (Stage IIIB or IV) Non-Small Cell Lung Cancer (NSCLC) Who Have Failed Previous Therapy With Platinum-Based Chemotherapy
研究概览
详细说明
DN-101 is an oral anti-cancer therapy for solid tumors and various hematologic malignancies. DN-101 is a unique formulation of calcitriol specifically designed for use in cancer. Calcitriol is a naturally occurring hormone and the most potent biologically active form of vitamin D. In high doses, calcitriol is active in many laboratory and animal models of cancer and synergistic with many commonly used chemotherapeutic agents. Until recently, the clinical use of calcitriol as an anti-cancer therapy was limited by hypercalcemia at doses required for anti-tumor activity. Based upon clinical results to date, Novacea believes it has successfully developed a solution to this problem through development of DN-101.
Chemotherapy for NSCLC, while not curative, has been shown to prolong survival in patients with unresectable disease. A number of different chemotherapy agents have been shown to have single-agent activity in NSCLC. These include cisplatin, carboplatin, vinorelbine, gemcitabine, paclitaxel and docetaxel. For first-line therapy of Stage IIIB or Stage IV NSCLC, these agents are generally used in combination. In most cases, first-line chemotherapy consists of a platinum-based agent, either cisplatin or carboplatin, and another chemotherapeutic.
Only one agent, Taxotere®, has been approved in the United States by the Food and Drug Administration for use as second-line chemotherapy in NSCLC.
研究类型
注册
阶段
- 阶段2
- 阶段1
联系人和位置
学习地点
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California
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Berkeley、California、美国、94704
- Alta Bates Comprehensive Cancer Center
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Vallejo、California、美国、94589
- Kaiser Permanente Medical Center (Northern California)
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Colorado
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Denver、Colorado、美国
- Rocky Mountain Cancer Center
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New York
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Albany、New York、美国
- New York Oncology Hematology, P.C. - Albany Regional Cancer Center
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North Carolina
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Winston-Salem、North Carolina、美国
- Piedmont Hematology Oncology Associates, PLLC
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Oklahoma
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Tulsa、Oklahoma、美国
- Cancer Care Associates
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Oregon
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Portland、Oregon、美国、97227
- Kaiser Permanente Northwest
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South Carolina
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Greenville、South Carolina、美国
- Cancer Centers of the Carolinas
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Washington
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Seattle、Washington、美国、98104
- Swedish Cancer Institute
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Vancouver、Washington、美国
- Northwest Cancer Specialists, P.C.
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Yakima、Washington、美国、98902
- Yakima Regional Cancer Care Center
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Histopathologically or cytologically proven non-small cell carcinoma of the lung (NSCLC), either Stage IIIB or Stage IV, that has progressed on or after first or second-line chemotherapy
- Measurable disease by RECIST criteria
- Eastern Cooperative Oncology Group (ECOG) Performance Status < 1
- Life expectancy > 3 months
- Age > 18 years
- Agrees to use adequate contraception throughout the treatment period and for at least 6 months following treatment
- Able to give informed patient consent
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 介入模型:单组作业
- 屏蔽:无(打开标签)
合作者和调查者
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
研究完成
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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