Prostate Cancer Clinical Trial

A Single Patient Compassionate Use of MBM-02 (Tempol) for the Treatment of Prostate Cancer

Summary

A single patient compassionate use clinical trial for the use of MBM-02 (TEMPOL) for the treatment of prostate cancer. The single patient will be exposed to orally administered TEMPOL for up to 12 months at a maximum total daily dose of 800mg.

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Full Description

Localized therapy for prostate cancer is often curative; however, 20% to 30% of patients experience a recurrence. Biochemical recurrence (BCR) occurs in an estimated 50,000 men/year in the U.S and is marked by a rising prostate specific antigen (PSA) after definitive radical prostatectomy and/or radiation therapy for localized disease.

Continuous androgen deprivation therapy (ADT), in which serum testosterone is decreased to a castrate level (less than 50 ng/dL) is a standard treatment in BCR. ADT is associated with significant short term and long term toxicities, including declining quality of life on treatment and increased risk of osteoporosis, diabetes, and cardiovascular disease. MBM-02 is being tested as a novel non-hormonal agent with improved biologic activity and better tolerability for use in biochemically recurrent prostate cancer.

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Eligibility Criteria

Inclusion Criteria:

Biochemical Recurrent Prostate Cancer

Exclusion Criteria:

-

Study is for people with:

Prostate Cancer

Study ID:

NCT04337099

Recruitment Status:

Available

Sponsor:

Matrix Biomed, Inc.

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There is 1 Location for this study

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Prostate Oncology Specialists
Marina Del Rey California, 90292, United States More Info
Krista Yasuda
Contact
Mark Scholz, MD
Principal Investigator

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Study ID:

NCT04337099

Recruitment Status:

Available

Sponsor:


Matrix Biomed, Inc.

How clear is this clinincal trial information?

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