A Single Patient Compassionate Use of MBM-02 (Tempol) for the Treatment of Prostate Cancer
Sponsor: Matrix Biomed, Inc.
ClinicalTrials ID:NCT04337099
This compassionate use trial involves MBM-02 (Tempol) for biochemically recurrent prostate cancer, aiming to offer a non-hormonal alternative to ADT, which has significant side effects. The single patient will receive 200 mg oral doses daily for up to 12 months. Eligibility is limited to those with biochemical recurrence, with no specified exclusion criteria.
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Program Overview
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.
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.
Eligibility Criteria
Inclusion Criteria
- Biochemical Recurrent Prostate Cancer
Exclusion Criteria
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