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Neoplasm Metastasis clinical trials

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NCT ID: NCT00656305 Completed - Multiple Myeloma Clinical Trials

ExAblate (MRgFUS) Treatment of Metastatic Bone Tumors for the Palliation of Pain

Start date: March 2008
Phase: N/A
Study type: Interventional

A Pivotal Study to Evaluate the Effectiveness and Safety of ExAblate Treatment of Metastatic Bone and Multiple Myeloma Tumors for the Palliation of Pain in Patients Who are not Candidates for Radiation Therapy

NCT ID: NCT00656123 Completed - Colorectal Cancer Clinical Trials

Study of Colon GVAX and Cyclophosphamide in Patients With Metastatic Colorectal Cancer

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

The primary objective of this study is to evaluate the safety and feasibility of vaccination with two irradiated allogeneic colorectal carcinoma cells administered with a GM-CSF producing bystander cell line in sequence with an immunomodulatory dose of Cyclophosphamide

NCT ID: NCT00652860 Completed - Sarcoma Clinical Trials

Combination Chemotherapy, Radiation Therapy, and Sargramostim Before and After Surgery in Treating Patients With Soft Tissue Sarcoma That Can Be Removed By Surgery

Start date: August 2001
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. GM-CSF may stimulate the immune system in different ways and stop tumor cells from growing. GM-CSF, given by inhalation, may interfere with the growth of tumor cells and prevent metastases from forming. Radiation therapy uses high energy x rays to kill tumor cells. Giving combination chemotherapy together with radiation therapy and GM-CSF before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving these treatments after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying how well giving combination chemotherapy together with radiation therapy and GM-CSF before and after surgery works in treating patients with stage III soft tissue sarcoma that can be removed by surgery.

NCT ID: NCT00649207 Completed - Neoplasm Metastasis Clinical Trials

A Phase I Study of ABT-888 in Combination With Conventional Whole Brain Radiation Therapy (WBRT) in Cancer Patients With Brain Metastases

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

This Phase I clinical trial is studying the side effects and best dose of ABT-888 when given together with Whole Brain Radiation Therapy (WBRT) in treating patients with brain metastases.

NCT ID: NCT00647348 Completed - Clinical trials for Secondary Progressive Multiple Sclerosis

Investigation of Simvastatin in Secondary Progressive Multiple Sclerosis

MS-STAT
Start date: January 2008
Phase: Phase 2
Study type: Interventional

To determine whether simvastatin at a dose of 80mg can reduce the rate of whole brain atrophy, as measured by MRI, over a 2-year time-period when compared to placebo.

NCT ID: NCT00645710 Completed - Liver Metastases Clinical Trials

Hepatic Arterial Infusion of Floxuridine, Gemcitabine Hydrochloride, and Radiolabeled Monoclonal Antibody Therapy in Treating Liver Metastases in Patients With Metastatic Colorectal Cancer Previously Treated With Surgery

Start date: February 11, 2005
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as floxuridine and gemcitabine hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Hepatic arterial infusion uses a catheter to carry cancer-killing substances directly into the liver. Radiolabeled monoclonal antibodies can find tumor cells and carry tumor-killing substances to them without harming normal cells. Giving hepatic arterial infusion of floxuridine together with gemcitabine hydrochloride and radiolabeled monoclonal antibody therapy after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase I/II trial is studying the side effects and best dose of floxuridine when given as a hepatic arterial infusion together with gemcitabine hydrochloride and radiolabeled monoclonal antibody therapy and to see how well it works in treating liver metastases in patients with metastatic colorectal cancer.

NCT ID: NCT00644319 Recruiting - Metastatic Cancer Clinical Trials

Ibuprofen or Morphine in Treating Pain in Patients Undergoing Pleurodesis for Malignant Pleural Effusion

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

RATIONALE: Morphine and ibuprofen help lessen pain caused by pleurodesis. It is not yet known whether one drug is more effective than the other in lessening pleurodesis-related pain or whether the size of the chest drain tube affects pain. PURPOSE: This randomized clinical trial is studying ibuprofen to see how well it works compared with morphine in treating pain in patients undergoing pleurodesis for malignant pleural effusion.

NCT ID: NCT00639262 Completed - Brain Metastases Clinical Trials

Combination of Sorafenib and Radiation for Brain Metastases and Primary Brain Tumors

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

Sorafenibâ„¢ has the potential to inhibit tumor growth, tumor angiogenesis , and enhance radiation response. This study will test the combination of Sorafenibâ„¢ and radiation therapy with or without temozolomide to determine tolerance of the combined treatments. Defining safe dosing of Sorafenibâ„¢ in this combination therapy will be achieved.

NCT ID: NCT00634582 Terminated - Prostate Cancer Clinical Trials

Paricalcitol in Treating Patients With Advanced Prostate Cancer and Bone Metastases

Start date: January 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: Paricalcitol may help prostate cancer cells become more like normal cells, and to grow and spread more slowly. It may also stop the growth of tumor cells in bone. PURPOSE: This phase II trial is studying how well paricalcitol works in treating patients with advanced prostate cancer and bone metastases.

NCT ID: NCT00633269 Completed - Neoplasm Metastasis Clinical Trials

Study Assessing Metabolism, Excretion and Pharmacokinetics of a Poly (ADP-Ribose) Polymerase (PARP) Inhibitor in Patients With Solid Metastatic Tumours

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

Open, non-randomized, radiolabelled, single centre study designed to characterize the metabolism, excretion and pharmacokinetics of a single oral dose of 100 mg [14C]-radiolabelled AZD2281 (KU-0059436) in patients with advanced or metastatic solid tumours.