Treatment of Metastatic Cancer in Terminally Diagnosed Patients

Purpose

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.

Condition

  • Metastatic Cancer

Eligibility

Eligible Ages
All ages
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • metastatic terminally diagnosed cancer

Exclusion Criteria

Study Design

Phase
Study Type
Expanded Access

Recruiting Locations

UCHealth University of Colorado Cancer Center - Anschutz Medical Campus
Aurora, Colorado 80045

More Details

Status
Available
Sponsor
Matrix Biomed, Inc.

Study Contact

Benji Crane
6264376506
bjcrane@matrixbiomed.com

Detailed 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.