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临床试验/NCT01945164
NCT01945164No Longer Available不适用

Single Patient Treatment Study for the Use of XL999 Administered Intravenously to a Subject With Advanced Malignancies Previously Enrolled in Study XL999-900

John Sarantopoulos1 个研究点 分布在 1 个国家开始时间: 2010年4月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
No Longer Available
发起方
试验地点
1

研究概览

简要总结

Cancer is a worldwide clinical and economic problem. Conventional approaches to treating cancer include surgery, radiotherapy, and cytotoxic chemotherapy as single modalities or as combined therapies. Recently, targeted therapies including antibodies and small molecule inhibitors have also demonstrated clinical benefit. It is now possible to study different genetic lesions involved in cancer types due to advances in genomic methodologies. The investigational drug in this study, XL999 inhibits multiple receptor tyrosine kinases, including VEGF receptor (VEGFR2/KDR), platelet derived growth factor receptors (PDGFRβ), fms-like tyrosine kinase receptor 3 (FLT3), fibroblast growth factor receptors (FGFR1, FGFR3), RET, and KIT, and thus, interferes with multiple cellular processes simultaneously and will likely have effects on the integrity of tumor neovasculature and angiogenesis. Together with the ability to induce a novel cell cycle arrest, the spectrum of activities that XL999 exhibits may reduce both tumor cell proliferation and angiogenesis in the clinic.

The rationale and purpose of this maintenance study is to allow a subject receiving clinical benefit from XL999 to continue treatment.

研究设计

研究类型
Expanded Access

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The subject is eligible to continue to receive XL999 in the absence of progressive disease and unacceptable XL999-related toxicity.

排除标准

  • Progressive disease.

研究者

发起方
John Sarantopoulos
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

John Sarantopoulos

Principal Investigator

The University of Texas Health Science Center at San Antonio

研究点 (1)

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