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Prostatic Neoplasms clinical trials

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NCT ID: NCT00059943 Completed - Breast Cancer Clinical Trials

Docetaxel in Treating Older Patients With Metastatic Breast, Lung, or Prostate Cancer

Start date: September 2002
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as docetaxel, use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: This phase II trial is studying how well docetaxel works in treating older patients with metastatic breast, lung, or prostate cancer.

NCT ID: NCT00059631 Completed - Prostate Cancer Clinical Trials

Phase I Study of Weekly Intravenous PS-341 (Bortezomib) Plus Mitoxantrone

Start date: March 20, 2003
Phase: Phase 1
Study type: Interventional

Primary Objective: -Establish the dose-limiting toxicity (DLT) and maximum tolerated dose (MTD) of weekly mitoxantrone in combination with weekly PS-341 in patients with advanced AI-PCa. Secondary objectives: - Evaluate the effect of bortezomib and mitoxantrone in combination on PSA levels among patients with baseline PSA levels >/=5 ng/mL who are treated near the maximum tolerated dose. - Monitor the effect of escalating doses of bortezomib combined with mitoxantrone on selected parameters of clinical benefit (i.e. performance status, tumor-related symptoms, measurable disease response).

NCT ID: NCT00058539 Completed - Prostate Cancer Clinical Trials

Safety and Efficacy Study of Pertuzumab to Treat Castration-Resistant Prostate Cancer

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

The purpose of this study is to evaluate safety and efficacy of Omnitarg (Pertuzumab) on cancerous lesions in men with castration-resistant (hormone-refractory) prostate cancer.

NCT ID: NCT00058253 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Combination Chemotherapy in Treating Patients With Metastatic or Unresectable Solid Tumors

Start date: February 2003
Phase: Phase 1
Study type: Interventional

This phase I trial is studying the side effects and best dose of combination chemotherapy in treating patients with metastatic or unresectable solid tumors. Drugs used in chemotherapy, such as docetaxel and 17-N-allylamino-17-demethoxygeldanamycin, work in different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells.

NCT ID: NCT00058084 Completed - Clinical trials for Adenocarcinoma of the Prostate

Ixabepilone Compared With Mitoxantrone and Prednisone in Treating Patients With Refractory Metastatic Prostate Cancer

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

This randomized phase II trial is studying ixabepilone to see how well it works compared to mitoxantrone and prednisone in treating patients with metastatic prostate cancer that has not responded to paclitaxel, docetaxel, or hormone therapy. Drugs used in chemotherapy work in different ways to stop tumor cells from dividing so they stop growing or die. Some tumors become resistant to chemotherapy drugs. Ixabepilone may reduce resistance to the drugs and allow the tumor cells to be killed. It is not yet known which chemotherapy regimen is more effective in treating metastatic prostate cancer

NCT ID: NCT00057759 Completed - Prostate Cancer Clinical Trials

Sildenafil in Treating Erectile Dysfunction in Patients With Prostate Cancer

Start date: January 2003
Phase: N/A
Study type: Interventional

RATIONALE: Sildenafil may be effective in helping patients who have undergone treatment for prostate cancer to have an erection for sexual activity and may improve sexual satisfaction and quality of life. PURPOSE: Randomized clinical trial to study the effectiveness of sildenafil in treating erectile dysfunction in patients who have undergone radiation therapy and hormone therapy for prostate cancer in clinical trial RTOG-9910.

NCT ID: NCT00056654 Completed - Prostatic Neoplasms Clinical Trials

Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prostate Cancer

Start date: March 2003
Phase: N/A
Study type: Interventional

The primary purpose of the study is to determine if a new sustained-release 45 mg (depot) formulation of leuprolide acetate will reduce serum testosterone levels to and maintain them at medically castrate levels in subjects with prostatic adenocarcinoma.

NCT ID: NCT00056407 Completed - Neoplasms, Prostate Clinical Trials

"REDUCE" - A Clinical Research Study To Reduce The Incidence Of Prostate Cancer In Men Who Are At Increased Risk

REDUCE
Start date: March 2003
Phase: Phase 3
Study type: Interventional

This 4-year study will compare how safe and effective an oral investigational medicine is (compared to placebo) in preventing the development of prostate cancer in men that are defined by the study entrance criteria as being at an increased risk for prostate cancer. Study visits to the clinic will occur every 6 months for up to 4 years (10 clinic visits), and a prostate biopsy will be performed at 2 and 4 years of treatment.

NCT ID: NCT00055731 Completed - Prostate Cancer Clinical Trials

Hormone Therapy With or Without Docetaxel And Estramustine in Treating Patients With Prostate Cancer That is Locally Advanced or At High Risk of Relapse

Start date: November 14, 2002
Phase: Phase 3
Study type: Interventional

RATIONALE: Androgens can stimulate the growth of prostate cancer cells. Drugs such as nilutamide, bicalutamide, flutamide, or cyproterone may stop the adrenal glands from producing androgens. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. It is not yet known whether hormone therapy is more effective with or without chemotherapy in treating prostate cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of hormone therapy with or without docetaxel and estramustine in treating patients who have prostate cancer that is locally advanced or at high risk of relapse.

NCT ID: NCT00055471 Completed - Prostatic Neoplasms Clinical Trials

A Phase IIa. Open-label, Multicenter, Dose-escalation Study to Assess the Tolerability and Pharmacokinetics of ZD4054 (Zibotentan) Given Orally Once Daily in Subjects With Metastatic Prostate Cancer

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

The primary purpose of this study is to determine the safest dose of ZD4054 (Zibotentan)in men with prostate cancer