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Prostatic Neoplasms clinical trials

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NCT ID: NCT00269555 Completed - Prostate Cancer Clinical Trials

Effects of GCP on Prostate Cancer.

Start date: May 2004
Phase: N/A
Study type: Interventional

Genistein Combined Polysaccharide (GCP) is derived from adding soy powder to shiitake mushrooms. This concentrated mixture is currently being sold in Japan and the United States and is thought to possibly contain properties that may be useful in treating certain types of cancer.

NCT ID: NCT00268892 Completed - Prostate Cancer Clinical Trials

Extension Study Investigating the Long-Term Safety of Degarelix Three-Month Depots in Patients With Prostate Cancer

Start date: January 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this extension study was to collect long-term safety and tolerability information to support a marketing authorisation application for a three-month dosage regimen of degarelix.

NCT ID: NCT00268710 Completed - Prostatic Neoplasms Clinical Trials

Docetaxel in Hormone Refractory Prostate Cancer (HRPC)[Weekly or 3weekly TAX + Prednisone in HRPC]

Start date: February 2004
Phase: Phase 2
Study type: Interventional

Primary objectives: - To determine the response rate, measurable and non measurable, to Taxotere® in the second line setting. Secondary objectives: - To evaluate the overall safety and toxicity of Taxotere®/prednisone combination as second line therapy in HRPC - To evaluate PSA response (PSA: Prostate Specific Antigen) - To evaluate symptomatic response - To evaluate Quality of life - To evaluate patient safety of weekly versus q3 weekly regimens of Taxotere®.

NCT ID: NCT00268593 Completed - Prostate Cancer Clinical Trials

Pilot Efficacy Study of PI-88 With Docetaxel to Treat Prostate Cancer

Start date: August 2005
Phase: Phase 2
Study type: Interventional

Docetaxel (Taxotere) is an approved chemotherapeutic drug for the treatment of androgen-independent prostate cancer. The aim of the study is to investigate whether addition of the investigational drug PI-88 will increase the efficacy of docetaxel in this disease. PI-88 inhibits cancer growth by inhibiting the development of new blood vessels and starving the tumour of oxygen and nutrients (anti-angiogenic). Because PI-88 and docetaxel have different mechanisms of action, they are expected to have increased (synergistic) activity when combined.

NCT ID: NCT00265070 Completed - Prostate Cancer Clinical Trials

Trial of Iressa in Prostate Cancer Patients

Start date: January 2003
Phase: Phase 2
Study type: Interventional

This study is being carried out to see if ZD1839 is effective in treating prostate cancer after being diagnosed with an early rising PSA (prostate specific antigen) following surgery.

NCT ID: NCT00264420 Completed - Breast Cancer Clinical Trials

Safety and Efficacy Study of Concomitant Radiotherapy and Zoledronic Acid for Bone Metastases Palliation

Start date: December 2005
Phase: Phase 1
Study type: Interventional

Zoledronic acid (Zometa) belongs to a class of drugs called bisphosphonates. Bisphosphonates are used in bone metastases to keep the cancerous lesion under control in the bone and to help prevent calcium level elevations in the blood. Cancer cell-culture studies at the Cleveland Clinic showed that zoledronic acid and radiation together have more cell killing effect than either one used alone. The purpose of this study is to monitor the healing of bone lesions when using zoledronic acid together with radiation treatment.

NCT ID: NCT00260611 Completed - Prostate Cancer Clinical Trials

Study of Oxaliplatin and Taxotere in Prostate Cancer

Start date: November 2004
Phase: Phase 2
Study type: Interventional

The primary objective for this study is to evaluate PSA response rates (response will be defined as a > 50% reduction in PSA levels) in men who have failed primary chemotherapy. The secondary objectives are to compare progression free survival, disease free survival, overall survival, and toxicity (tolerance/safety).

NCT ID: NCT00258401 Completed - Prostate Cancer Clinical Trials

Low-Residue Diet in Treating Diarrhea in Patients Receiving Pelvic Radiation Therapy.

Start date: May 2005
Phase: N/A
Study type: Interventional

RATIONALE: Eating a diet low in residue (fiber, fat, and certain milk or vegetable products) may help prevent or reduce diarrhea caused by pelvic radiation therapy. PURPOSE: This randomized clinical trial is studying a low-residue diet to see how well it works compared to no dietary intervention in treating diarrhea in patients who are undergoing radiation therapy to the pelvis for uterine, cervical, or prostate cancer.

NCT ID: NCT00258388 Completed - Prostate Cancer Clinical Trials

Docetaxel and Prednisone With/Out OGX-011 in Recurrent or Metastatic Prostate Cancer That Did Not Respond to Previous Hormone Therapy

Start date: September 28, 2005
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as docetaxel and prednisone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. OGX-011 may help docetaxel and prednisone kill more tumor cells by making tumor cells less resistant to the drugs. PURPOSE: This randomized phase II trial is studying how well giving docetaxel and prednisone with or without OGX-011 works in treating patients with recurrent or metastatic prostate cancer that did not respond to previous hormone therapy.

NCT ID: NCT00258284 Completed - Prostate Cancer Clinical Trials

Capecitabine and Docetaxel in Treating Patients With Metastatic Prostate Cancer

Start date: August 2003
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as capecitabine and docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving capecitabine together with docetaxel works in treating patients with metastatic prostate cancer.