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Clinical Trial Summary

This is a non-randomized, open-label study in patients with newly diagnosed glioblastoma to determine the ability to generate human hybridomas from lymph nodes draining an autologous tumor vaccine injection and demonstrate that the hybridomas secrete glioblastoma-specific antibodies.


Clinical Trial Description

The intradermal vaccine will be injected 20cm in the anterior thigh. Vaccination will be done twice and separated by one week. The first vaccination will be performed approximately 2 weeks after surgery.

Approximately one week after the second vaccination one or two vaccine-draining lymph node(s) will be removed. The lymph node(s) will be identified using SN technology. One or two lymph node(s) will be removed.

Lymph nodes will be processed for recovery of B cells and formation of hybridomas. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01702792
Study type Interventional
Source Dartmouth-Hitchcock Medical Center
Contact
Status Terminated
Phase Phase 1
Start date January 2014
Completion date May 6, 2015

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