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Clinical Trial Summary

The purpose of this study is to further quantify the risk of cerebrovascular events (CVEs) following sipuleucel-T (PROVENGE®) therapy, and to follow all subjects for survival.


Clinical Trial Description

Subjects will receive product as described in the sipuleucel-T approved label. The registry will be strictly observational and thus no additional clinical visits or laboratory tests will be conducted beyond normal clinical practice. Investigators will be asked to record information that becomes available in the normal course of clinical management. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01306890
Study type Observational
Source Dendreon
Contact
Status Completed
Phase
Start date January 27, 2011
Completion date January 17, 2017

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