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Clinical Trial Summary

This feasibility study will assess the effects of the Nativis Voyager therapy in patients with recurrent GBM who have either failed standard of care or are intolerant to therapy. The study will enroll and treat up to eleven subjects over six months. Safety and clinical utility will be evaluated.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02507102
Study type Interventional
Source Nativis, Inc.
Contact
Status Completed
Phase N/A
Start date August 2015
Completion date March 26, 2018

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