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NCT ID: NCT00052156 Active, not recruiting - Malignant Melanoma Clinical Trials

Vaccine Therapy for Patients With Stage IV Melanoma

Start date: n/a
Phase: Phase 3
Study type: Interventional

This is a Phase III study in patients with melanoma that has spread to the lymph nodes and/or a distant organ, and who have had all of their cancer surgically removed. The purpose of this study is to evaluate the ability of the CancerVax™ vaccine to prevent or slow the recurrence of melanoma.

NCT ID: NCT00052130 Active, not recruiting - Malignant Melanoma Clinical Trials

Vaccine Therapy for Patients With Stage III Melanoma

Start date: n/a
Phase: Phase 3
Study type: Interventional

This is a Phase 3 study in patients with melanoma that has spread to the lymph nodes (stage III), and who have had all of their cancer surgically removed. The purpose of this study is to evaluate the ability of the CancerVax™ vaccine to prevent or slow the recurrence of melanoma.

NCT ID: NCT00051051 Completed - Breast Neoplasms Clinical Trials

A Phase II Study of CI-1033 in Treating Patients With Metastatic (Stage IV) Breast Cancer

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

CI-1033 is an experimental drug that acts as an inhibitor of erbB (EGFR) receptors, which may be involved in tumor growth. The primary objective of this study is to assess the antitumor activity of CI-1033 in patients with metastatic breast cancer. Patients with histologically confirmed metastatic (Stage IV) breast cancer and who have received no more than 2 prior cytotoxic chemotherapy regimens are eligible for this study. CI-1033 is administered orally. Patients are required to have blood tests periodically while receiving treatment and will be closely monitored throughout the study for possible side effects and response to treatment. Patients may not have received any prior treatment with other agents that target erbB receptors, including Herceptin (trastuzumab) or Iressa (gefitinib).

NCT ID: NCT00050830 Completed - Lung Neoplasms Clinical Trials

A Phase 2, Randomized, Open-Label Study Of Single Agent CI-1033 In Patients With Advanced Non-Small Cell Lung Cancer

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

The purpose of study to determine the activity of CI 1033 against tumors in patients with advanced or metastatic NSCLC who have failed prior platinum-based combination chemotherapy. Another objective is to determine the safety of CI 1033.

NCT ID: NCT00048659 Terminated - Prostatic Neoplasms Clinical Trials

YM598 Added to Mitoxantrone/Prednisone to Control Pain in Metastatic Prostate Cancer Patients No Longer Responding to Hormone Therapy

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if patients who take YM598 in addition to mitoxantrone and prednisone (standard therapy) experience improvement in the pain associated with prostate cancer metastases in the bone.

NCT ID: NCT00048230 Completed - Multiple Myeloma Clinical Trials

PS-341 (VELCADE™) Versus High-Dose Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma

Start date: June 2002
Phase: Phase 3
Study type: Interventional

This study will compare the efficacy of PS-341 versus high dose dexamethasone.

NCT ID: NCT00045032 Active, not recruiting - Breast Cancer Clinical Trials

Trastuzumab in Treating Women With Primary Breast Cancer

Start date: December 2001
Phase: Phase 3
Study type: Interventional

RATIONALE: Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. It is not yet known whether trastuzumab is effective in treating primary breast cancer in women who have completed adjuvant chemotherapy. PURPOSE: This randomized phase III trial is studying two different regimens of trastuzumab and observation only to compare how well they work in treating women with breast cancer.

NCT ID: NCT00038467 Completed - Breast Neoplasms Clinical Trials

Randomized Trial Of Exemestane Versus Continued Tamoxifen In Postmenopausal Women With Early Breast Cancer

IES
Start date: February 1998
Phase: Phase 3
Study type: Interventional

To compare the sequential administration of exemestane with administration of further tamoxifen until 5 years in postmenopausal women with operable breast cancer who have already received 2-3 years of adjuvant tamoxifen, in terms of disease-free survival (DFS), overall survival (OS), incidence of contralateral breast cancer and long-term tolerability.

NCT ID: NCT00036556 Completed - Prostatic Neoplasms Clinical Trials

Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Cancer

Start date: June 2001
Phase: Phase 3
Study type: Interventional

This study is being done to evaluate the safety and efficacy of atrasentan in men with non-metastatic hormone-refractory prostate cancer.

NCT ID: NCT00036543 Completed - Prostate Cancer Clinical Trials

A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer

Start date: May 2001
Phase: Phase 3
Study type: Interventional

This study is being done to evaluate the safety and efficacy of atrasentan in men with metastatic hormone-refractory prostate cancer.