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Prostate Cancer clinical trials

View clinical trials related to Prostate Cancer.

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NCT ID: NCT00673127 Completed - Prostate Cancer Clinical Trials

Ketoconazole, Hydrocortisone and Dutasteride in Asymptomatic Hormone Refractory Prostate Cancer

KHAD
Start date: February 2005
Phase: Phase 2
Study type: Interventional

The combination of ketaconazole and hydrocortisone is commonly used for the treatment of prostate cancer. The purpose of this study is to determine if the addition of a drug called dutasteride to this approved combination will make the combination more effective in treating prostate cancer.

NCT ID: NCT00672594 Completed - Prostate Cancer Clinical Trials

Study of Sunitinib Malate in Patients With Newly Diagnosed Prostate Cancer Prior to Prostatectomy

Start date: July 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to look at blood and tissue samples for changes following the use of Sunitinib malate. Additionally, we would like to find out if the drug, Sunitinib malate, is safe and works in men with prostate cancer. Sunitinib malate , also known as Sutent, is approved by the U.S. Food and Drug Administration (FDA), for treatment of tumors of intestines and kidney but it is being tested in research studies for use in men with prostate cancer.

NCT ID: NCT00670553 Completed - Prostate Cancer Clinical Trials

A Phase I Study of LBH589 (Panobinostat) in Combination With External Beam Radiotherapy for the Treatment of Prostate Cancer, Esophageal Cancer and Head and Neck Cancer

Start date: September 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the feasibility of combined administration of different LBH589 dosages with radiotherapy in order to establish the dosage to be evaluated in future studies.

NCT ID: NCT00669656 Completed - Prostate Cancer Clinical Trials

Herbal Therapy for Treatment of Recurrent Prostate Cancer

Start date: July 6, 2008
Phase: Phase 2
Study type: Interventional

This study is about Prostate Health Cocktail, a combination supplement that contains vitamin D3, vitamin E, selenium, green tea extract, saw palmetto, lycopene, and soy derivatives. This product is currently available on the market, as herb and vitamin supplements are not regulated by the FDA. Each ingredient has been studied in prostate cancer cells and/or in patients with prostate cancer. At the doses included in this supplement, no serious side effects have been reported. The purpose of this study is to find out whether Prostate Health Cocktail can lower your PSA. Additionally, we will be looking to see whether taking this treatment causes any unexpected side effects, and whether certain blood tests can inform us about your disease status in addition to your PSA

NCT ID: NCT00669162 Completed - Prostate Cancer Clinical Trials

Postoperative Radiation Therapy, Hormonal Therapy and Concurrent Docetaxel for High Risk Pathologic Prostate Cancer

Start date: August 2012
Phase: Phase 1/Phase 2
Study type: Interventional

Following a radical prostatectomy and lymph node sampling, eligible patients will undergo post-operative radiation therapy, concurrent weekly docetaxel chemotherapy , and hormonal therapy (Casodex daily and Zoladex every 3 months for 2 times or Lupron 22.5 mg im every 3 months for 2 times).

NCT ID: NCT00668642 Completed - Prostate Cancer Clinical Trials

Effect of Dutasteride on Androgen-Response Gene Expression in Patients With Advanced Prostate Cancer

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if the drug dutasteride increases expression of genes that slow the growth of prostate cancer during treatment with intermittent androgen ablation therapy (hormone therapy).

NCT ID: NCT00668083 Completed - Prostate Cancer Clinical Trials

Observational Retrospective Trial on Sequential Hormonal Therapy in Patients With Prostate Cancer

Sorse
Start date: September 2007
Phase: N/A
Study type: Observational

Observational Retrospective trial on sequential hormonal therapy in patients with Prostate Cancer

NCT ID: NCT00667862 Completed - Prostate Cancer Clinical Trials

Efficacy and Safety Study of Panobinostat in Participants With Metastatic Hormone Refractory Prostate Cancer

Start date: March 18, 2008
Phase: Phase 2
Study type: Interventional

This Phase II single dose study was designed to characterize the safety, tolerability, and efficacy of intravenous (i.v.) panobinostat as a single-agent treatment in participants with hormone refractory prostate cancer.

NCT ID: NCT00667641 Completed - Breast Cancer Clinical Trials

Paclitaxel and Bortezomib in Treating Patients With Metastatic or Unresectable Malignant Solid Tumors

Start date: March 2007
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving paclitaxel together with bortezomib may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of paclitaxel and bortezomib in treating patients with metastatic or unresectable malignant solid tumors.

NCT ID: NCT00664456 Completed - Prostate Cancer Clinical Trials

Luteinizing Hormone-Releasing Hormone Agonist Therapy and Iodine I 125 Implant in Treating Patients With Previously Untreated Prostate Cancer

SHIP0804
Start date: April 2008
Phase: Phase 3
Study type: Interventional

RATIONALE: Androgens can cause the growth of prostate cancer cells. Luteinizing hormone-releasing hormone agonists may lessen the amount of androgens made by the body. Internal radiation uses radioactive material placed directly into or near a tumor to kill tumor cells. Giving luteinizing hormone-releasing hormone agonist together with an iodine I 125 implant may be an effective treatment for patients with prostate cancer. PURPOSE: This randomized phase III trial is studying how well giving luteinizing hormone-releasing hormone agonist therapy together with an iodine I 125 implant works with or without additional luteinizing hormone-releasing hormone agonist therapy in treating patients with previously untreated prostate cancer.