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Clinical Trial Summary

The objective is to provide terminally diagnosed patients with a last line of treatment while improving overall quality of life. Tempol can be added to any chemotherapy regimen to potentially reduce side effects and overcome chemoresistance.


Clinical Trial Description

The objective is to provide terminally diagnosed patients assigned to palliative care and palliative chemotherapy a last line treatment with Tempol. In vivo studies have shown Tempol to work synergistically with a number of chemotherapy agents increasing treatment response and reducing chemoresistance. Additionally, Tempol has been shown to provide protection to non-cancerous cells allowing for increased chemotherapy dosing by reducing side effects. Tempol inhibits HIF-1/VEGF among others in cancerous cells while upregulating GSH/NrF2 among others in non-cancerous cells. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05491928
Study type Expanded Access
Source Matrix Biomed, Inc.
Contact Benji Crane
Phone 6264376506
Email bjcrane@matrixbiomed.com
Status Available
Phase

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