Prostate Cancer

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Educational Needs of Patients Undergoing Watchful Waiting for Localized Prostate Cancer

RATIONALE: Gathering information about anxiety and depression in patients with localized prostate cancer who have selected watchful waiting may help doctors develop educational materials that help patients cope with cancer-related anxiety. PURPOSE: This study is looking at the educational needs of patients who are undergoing watchful waiting for localized prostate cancer.

Background information
Other unique IDs: 
CDR0000600452
BCM-H-19995

Docetaxel and Cetuximab in Treating Patients With Metastatic Prostate Cancer

RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Cetuximab may also stop the growth of prostate cancer by blocking blood flow to the tumor. Giving docetaxel together with cetuximab may kill more tumor cells. PURPOSE: This phase II trial is studying the side effects of giving docetaxel together with cetuximab and to see how well it works in treating patients with metastatic prostate cancer.

Background information
Other unique IDs: 
CDR0000599858
SWS-SAKK-08/07
MERCK-SAKK-0807
SANOFI-AVENTIS-SWS-SAKK-0807

Open-Label, Randomised Parallel-Group Study

Trial phase: 
Phase III
Recruitment status: 
Terminated

An Open-Label, Multi-Centre, Randomised Parallel-Group Study, Investigating Efficacy and Safety of Different Degarelix Three-Month Dosing Regimens in Patients with Prostate Cancer Requiring Androgen Ablation Therapy.

Background information
Trial ID: 
NCT00728533
Other unique IDs: 
FE 200486 CS26
2007-006055-39
Official title: 

The Rationale of the Study is to Demonstrate That Degarelix Given at Three-Month Dosing Intervals Will Produce and Maintain Androgen Deprivation in Prostate Cancer Patients Through Immediate and Prolonged Testosterone Suppression, and to Provide Confirmat

Detailed description: 

 

Number to be enrolled: 
0 patients

Hydroxychloroquine in Treating Patients With Rising PSA Levels After Local Therapy for Prostate Cancer

RATIONALE: Hydroxychloroquine may stop the growth of tumor cells by blocking some of the cellular functions needed for cells to survive. PURPOSE: This phase II trial is studying how well hydroxychloroquine works in treating patients with rising prostate-specific antigen (PSA) levels after local therapy for prostate cancer.

Background information
Other unique IDs: 
CDR0000600326
CINJ-080803

A Study Of the Effectiveness Of Pomegranate Pills in Men With Prostate Cancer Before Prostatectomy

Recruitment status: 
Recruiting

The purpose of this study is to compare the effects of pomegranate polyphenol pills (POM-X) and a placebo (sugar pill) on prostatic oxidative stress. The placebo is a pill that looks like the POM-X pill but does not have an active ingredient.

Background information
Trial ID: 
NCT00719030
Other unique IDs: 
GUP-0515-02
Official title: 

A Randomized, Placebo-Controlled, Pre-Surgical Study of the Effects of Pomegranate Pills in Men With Prostate Cancer Prior to Radical Prostatectomy

Detailed description: 

Subjects will receive POM-X or placebo pills daily for up to 4 weeks prior to undergoing radical prostatectomy for prostate cancer. Biomarkers in the blood, urine, and prostate tissue will be assessed.

Number to be enrolled: 
35 patients

A Phase I/II Study of HE3235 in Patients With Prostate Cancer

Trial phase: 
Phase II
Recruitment status: 
Recruiting

This is a phase I/II, open-label, dose escalation study of HE3235 administered orally to patients with advanced prostate cancer who have failed hormone therapy and at least one taxane based chemotherapy regimen.

Background information
Trial ID: 
NCT00716794
Other unique IDs: 
HE3235-0201
Official title: 

A Phase I/II, Open-Label, Dose Ranging Study of the Safety, Tolerance, Pharmacokinetics and Potential Activity of HE3235 When Administered Orally to Patients With Prostate Cancer

Detailed description: 

 

Number to be enrolled: 
44 patients

Sipuleucel-T as Neoadjuvant Treatment in Prostate Cancer

Trial phase: 
Phase II
Recruitment status: 
Recruiting

This is an open label, Phase 2 trial of immunotherapy with sipuleucel-T as neoadjuvant treatment in men with localized prostate cancer.

Background information
Trial ID: 
NCT00715104
Other unique IDs: 
P07-1
Official title: 

A Single Center, Open Label, Phase 2 Trial of Immunotherapy With Sipuleucel-T as Neoadjuvant Treatment in Men With Localized Prostate Cancer

Detailed description: 

This is a single center, open label, Phase 2 study. Subjects will be treated with 3 infusions of sipuleucel-T prior to a scheduled radical prostatectomy (RP) surgery. To assess the immune response following treatment with sipuleucel-T, tissue from the prostatectomy specimen will be compared with tissue from the core biopsy specimen obtained prior to treatment with sipuleucel T. Following RP, subjects will be randomized to receive either a booster infusion of sipuleucel T or no further treatment with sipuleucel-T (i.e., booster: no booster).

Number to be enrolled: 
40 patients
Acronym: 
NeoACT

To Evaluate Sipuleucel-T Manufactured With Different Concentrations of PA2024 Antigen

This is a randomized, multicenter, single blind, Phase 2 trial of immunotherapy in men with metastatic androgen independent prostate cancer to evaluate sipuleucel-T manufactured with different concentrations of PA2024 antigen

Background information
Other unique IDs: 
P07-2

Internal Radiation Therapy With or Without External-Beam Radiation Therapy in Treating Patients With Localized Prostate Cancer

RATIONALE: Internal radiation uses radioactive material placed directly into or near a tumor to kill tumor cells. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. PURPOSE: This phase II trial is studying the side effects of internal radiation therapy when given with or without external-beam radiation therapy and to see how well it works in treating patients with localized prostate cancer.

Background information
Other unique IDs: 
CDR0000600446
MAYO-MC0652

Phase II Study of Docetaxel for Clinically Asymptomatic High Risk Prostate Cancer Patients

The purpose of this study is to assess the response to Taxotere (docetaxel) chemotherapy given as a primary treatment to patients with early and rapid PSA rising after prostatectomy for high risk disease.

Background information
Other unique IDs: 
Project 5.2.08.02
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