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Clinical Trial Summary

The main purpose of this part of the study is to determine the Central Nervous System bioavailability of sulfasalazine.


Clinical Trial Description

This is a pilot, open-label, non-randomized, study to determine the effect that orally administered sulfasalazine has on glutamate levels as measured by MRS and on epileptiform spiking as measured by simultaneous MEG/EEG. The intent of the dose escalation is to determine an Optimal Biological Dose (OBD) based on changes in tumor glutamate levels. The OBD is defined as the dose that has the maximal reduction in tumor glutamate levels after normalization to uninvolved brain. ;


Study Design

Endpoint Classification: Bio-availability Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01577966
Study type Interventional
Source University of Alabama at Birmingham
Contact
Status Completed
Phase N/A
Start date January 2012
Completion date January 2015

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