Brief Summary

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

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.

Available
Individual Patients
Metastatic Cancer

Drug: Tempol

Tempol will be given as an adjunct to chemotherapy.
Other Name: MBM-0-1 MBM-02

Eligibility Criteria

Inclusion Criteria:

- metastatic terminally diagnosed cancer

Exclusion Criteria:

-

Eligibility Gender
All
Eligibility Age
Minimum: N/A ~ Maximum: N/A
Countries
United States
Locations

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

Contacts

Benji Crane
6264376506
bjcrane@matrixbiomed.com

Matrix Biomed, Inc.
NCT Number
MeSH Terms
Neoplasm Metastasis
Tempol