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Neoplasm Metastasis clinical trials

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NCT ID: NCT01115803 Terminated - Clinical trials for Renal Cell Carcinoma

A Study of LY2584702 With Erlotinib or Everolimus in Participants With Solid Tumors

Start date: March 2010
Phase: Phase 1
Study type: Interventional

Study I3G-MC-JGCB (JGCB) is a multicenter, nonrandomized, open-label, dose-escalation Phase 1b study of LY2584702 in combination with either erlotinib or everolimus.

NCT ID: NCT01089595 Terminated - GIST Clinical Trials

Trial of Tasigna (Nilotinib) 400 mg Twice Daily Alone or With Gleevec (Imatinib Mesylate) 400 mg Daily for Patients With Advanced Gastrointestinal Stromal Tumor (GIST)

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

Patients with advanced GIST are treated with imatinib. This study seeks to look at a new therapeutic agent at the time of tumor progression following treatment with 600-800 mg daily of imatinib. The study is looking to see if Nilotinib (tasigna) alone or in combination with imatinib (gleevec) is more effective at controlling disease.

NCT ID: NCT01081808 Terminated - Neoplasms Clinical Trials

Laboratory-Treated Autologous Lymphocytes, Aldesleukin, and Sargramostim (GM-CSF) in Treating Advanced Solid Tumors

Start date: October 2009
Phase: Phase 1
Study type: Interventional

RATIONALE: Giving autologous lymphocytes that have been treated in the laboratory with antibodies may stimulate the immune system to kill tumor cells. Aldesleukin may stimulate the lymphocytes to kill tumor cells. Colony-stimulating factors, such as GM-CSF, may increase the number of immune cells found in bone marrow or peripheral blood. Giving laboratory-treated autologous lymphocytes together with aldesleukin and GM-CSF may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of laboratory-treated autologous lymphocytes when given together with aldesleukin and GM-CSF in treating patients with recurrent, refractory, or metastatic advanced solid tumors.

NCT ID: NCT01077869 Terminated - Clinical trials for Squamous Cell Carcinoma of the Oral Cavity

A Feasibility Study on the Use of F-18-FDG-PET and Optical Imaging in Evaluation of Radiation-induced Oral Mucositis

Start date: January 2010
Phase: Phase 1
Study type: Observational

In this study, the feasibility of optical imaging and FDG-PET in the evaluation of radiation-induced mucositis will be evaluated.

NCT ID: NCT01076270 Terminated - Clinical trials for Recurrent Mantle Cell Lymphoma

Plerixafor and Filgrastim For Mobilization of Donor Peripheral Blood Stem Cells Before A Donor Peripheral Blood Stem Cell Transplant in Treating Patients With Hematologic Malignancies

Start date: June 2010
Phase: N/A
Study type: Interventional

RATIONALE: Giving chemotherapy and total-body irradiation (TBI) before a donor peripheral blood stem cell transplant helps stop the growth of cancer cells and helps stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells from a donor are infused into the patient they will help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Giving colony-stimulating factors, such as filgrastim (G-CSF) and plerixafor, to the donor helps the stem cells move (mobilization) from the bone marrow to the blood so they can be collected and stored. PURPOSE: This clinical trial is studying giving plerixafor and filgrastim together for mobilization of donor peripheral blood stem cells before a peripheral blood stem cell transplant in treating patients with hematologic malignancies

NCT ID: NCT01071941 Terminated - Liver Metastases Clinical Trials

rRp450-Phase I Trial in Liver Metastases and Primary Liver Tumors

Start date: October 2010
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to determine the safety of rRp450 and the highest dose of this agent that can be given to people safely. We are also looking to see how well the body tolerates the study agent, how the agent is absorbed by the liver cancers, how quickly the agent is eliminated from the body, and what kind of anti-cancer effect it may have. rRp450 is a type of gene therapy and a form of the Herpes simplex virus 1 (or HSV). HSV is a virus that usually causes cold sores of the mouth. In extremely rare circumstances, this virus can cause severe infections, such as an infection of the brain. rRp450 was developed from an HSV and specially altered to target and kill cancer cells.

NCT ID: NCT01030757 Terminated - Liver Cancer Clinical Trials

Study of Stereotactic Body Radiation Therapy Using Tomotherapy for Metastatic Tumors to the Liver

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

The purpose of this study is to determine the response of liver tumors to radiation therapy using Tomotherapy.

NCT ID: NCT01020305 Terminated - Prostate Cancer Clinical Trials

Temsirolimus to Reverse Androgen Insensitivity for Castration-resistant Prostate Cancer

Start date: October 2009
Phase: Phase 1/Phase 2
Study type: Interventional

This study evaluates if temsirolimus causes a reduction in the serum levels of prostate-specific antigen (PSA) in male subjects with castration-resistant prostate cancer (CRPC).

NCT ID: NCT01018836 Terminated - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Riluzole and Whole-Brain Radiation Therapy in Treating Patients With Brain Metastases

Start date: November 2009
Phase: Phase 1
Study type: Interventional

RATIONALE: Radiation therapy uses high energy x-rays to kill tumor cells. Drugs, such as riluzole, may make tumor cells more sensitive to radiation therapy. Giving riluzole together with whole-brain radiation therapy may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of riluzole when given together with whole-brain radiation therapy in treating patients with brain metastases.

NCT ID: NCT00981578 Terminated - Bone Metastases Clinical Trials

ExAblate Conformal Bone System Treatment of Metastatic Bone Tumors for the Palliation of Pain

Start date: September 2009
Phase: N/A
Study type: Interventional

A study to evaluate the safety and initial effectiveness of the ExAblate 2100 Conformal Bone System in the treatment of pain resulting from metastatic bone tumors.