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Clinical Trial Summary

The main purpose of this research study is to evaluate the safety and dosing of CG0070.


Clinical Trial Description

Cohorts of three to six patients will be assigned to receive intravesical (into the bladder) administration of CG0070 either Weekly or Every 4 Weeks for up to a total of 6 doses. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00109655
Study type Interventional
Source Cell Genesys
Contact
Status Active, not recruiting
Phase Phase 1
Start date April 2005
Completion date September 2010

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