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Clinical Trial Summary

This is an open label, non-randomized, single site Phase I study to test the manufacturing feasibility and safety of locoregional (LR) administration of B7-H3CART into the central nervous system of adult subjects with recurrent IDH wild-type GBM using a standard 3+3 dose escalation design.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05474378
Study type Interventional
Source Stanford University
Contact Kelly Tanner
Phone 650-724-5361
Email ketanner@stanford.edu
Status Recruiting
Phase Phase 1
Start date July 12, 2022
Completion date August 2025

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