Tetrathiomolybdate in Hormone Refractory Prostate Cancer
Recruitment status was Active, not recruiting
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Purpose: The aim of this clinical trail is to evaluate Tetrathiomolybdate (TM) in the treatment of hormone refractory prostate cancer.
Condition | Intervention | Phase |
---|---|---|
Prostate Cancer |
Drug: tetrathiomolybdate |
Phase 2 |
Study Type: | Interventional |
Study Design: | Allocation: Non-Randomized Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
Official Title: | A Phase II Trail of Tetrathiomolybdate in Patients With Hormone Refractory Prostate Cancer |
- To determine the time to progression and pattern of progression of prostate cancer in patients with androgen-independent prostate cancer treated with tetrathiomolybdate.
Estimated Enrollment: | 37 |
Study Start Date: | May 2001 |
Tetrathiomolybdate or TM, a drug developed for Wilson's Disease, removes copper from the bloodstream. Copper is a key factor in angiogenesis (blood vessel growth)- a process that occurs normally in the body but becomes uncontrolled in cancerous cells. Tetrathiomolybdate essentially wages war against copper, which serves to choke off tumor growth. Realizing the key role of copper in angiogenesis, researchers have begun exploring treatment with Tetrathiomolybdate for different types of cancers. This clinical trial will evaluate the effectiveness of Tetrathiomolybdate in the treatment of patients with hormone refractory prostate cancer. Hormone refractory prostate cancer refers to advanced disease in which the patient no longer responding to conventional hormonal treatment.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Male |
Accepts Healthy Volunteers: | No |
Patients must have histologic diagnosis of adenocarcinoma of the prostate with progression following hormonal therapy and antiandrogen withdrawal.
United States, Michigan | |
The University of Michigan Comprehensive Cancer Center | |
Ann Arbor, Michigan, United States, 48109 |
Principal Investigator: | David C. Smith, MD | The University of Michigan Comprehensive Cancer Center |
No publications provided
ClinicalTrials.gov Identifier: | NCT00150995 History of Changes |
Other Study ID Numbers: | UMCC 9962 |
Study First Received: | September 6, 2005 |
Last Updated: | September 6, 2005 |
Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
Prostatic Neoplasms Genital Neoplasms, Male Urogenital Neoplasms Neoplasms by Site Neoplasms Genital Diseases, Male Prostatic Diseases Hormones Tetrathiomolybdate Molybdenum Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs |
Pharmacologic Actions Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Angiogenesis Inhibitors Angiogenesis Modulating Agents Growth Substances Growth Inhibitors Antineoplastic Agents Therapeutic Uses Chelating Agents Trace Elements Micronutrients |
ClinicalTrials.gov processed this record on October 16, 2012