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Melanoma clinical trials

View clinical trials related to Melanoma.

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NCT ID: NCT01659151 Active, not recruiting - Metastatic Melanoma Clinical Trials

Vemurafenib With Lymphodepletion Plus Adoptive Cell Transfer & High Dose IL-2 Metastatic Melanoma

Start date: August 3, 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to find out more about the effects of an investigational combination of medicines, which includes special immune cells (T-cells). A T-cell is a type of lymphocyte, or white blood cell. Lymphocytes are a kind of white blood cell that protect the body from viral infections, help other cells fight bacterial and fungal infections, produce antibodies, fight cancers, and coordinate the activities of other cells in the immune system.

NCT ID: NCT01644591 Active, not recruiting - Metastatic Melanoma Clinical Trials

Stereotactic Radiosurgery in Treating Patients With Greater Than 3 Melanoma Brain Metastases

Start date: August 2, 2012
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well stereotactic radiosurgery works in treating patients with melanoma that has spread to more than 3 places in the brain. Stereotactic radiosurgery is a specialized radiation therapy that delivers a single, high dose of radiation directly to the tumor and may cause less damage to normal tissue.

NCT ID: NCT01638533 Active, not recruiting - Lymphoma Clinical Trials

Romidepsin in Treating Patients With Lymphoma, Chronic Lymphocytic Leukemia, or Solid Tumors With Liver Dysfunction

Start date: June 12, 2012
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of romidepsin in treating patients with lymphoma, chronic lymphocytic leukemia, or solid tumors with liver dysfunction. Romidepsin may stop the growth of cancer cells by entering the cancer cells and by blocking the activity of proteins that are important for the cancer's growth and survival.

NCT ID: NCT01620749 Active, not recruiting - Metastatic Melanoma Clinical Trials

Of 18F MEL050 Using PET/CT in Metastatic Melanoma

MEL050
Start date: June 2010
Phase: Phase 0
Study type: Interventional

The purpose of this study is to investigate the safety and potential effectiveness of the imaging compound 18F MEL050 for finding sites of melanoma.

NCT ID: NCT01590069 Active, not recruiting - Sarcoma Clinical Trials

Aerosolized Aldesleukin in Treating Patients With Lung Metastases

Start date: June 28, 2012
Phase: Phase 1
Study type: Interventional

This phase I/II trial studies the side effects and best dose of aerosolized aldesleukin and to see how well it works in treating patients with cancer that has spread from the original tumor to the lungs. Biological therapies, such as aerosolized aldesleukin, may stimulate or suppress the immune system in different ways and stop tumor cells from growing.

NCT ID: NCT01587352 Active, not recruiting - Clinical trials for Metastatic Uveal Melanoma

Vorinostat in Treating Patients With Metastatic Melanoma of the Eye

Start date: May 29, 2012
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well vorinostat works in treating patients with melanoma of the eye that has spread to other parts of the body (metastatic). Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

NCT ID: NCT01586767 Active, not recruiting - Melanoma Clinical Trials

Intensity-Modulated or Proton Radiation Therapy for Sinonasal Malignancy

Start date: July 12, 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to test the hypothesis that 1)intensity-modulated radiotherapy (IMRT) or proton radiation therapy would result in improved local control rate and lowered toxicity compared to conventional radiotherapy, and 2) proton radiation therapy would result in equivalent or improved local control rate with similar or lower toxicity compared to IMRT, in the treatment of locally advanced sinonasal malignancy. Data from retrospective studies suggest that IMRT or proton radiation therapy resulted in promising outcome in patients with sinonasal malignancy. To this date, no prospective study has been conducted to evaluate the outcome of sinonasal cancer treated with IMRT or proton radiation therapy. This Phase II trial is the first prospective study conducted to determine the treatment outcome and toxicity of IMRT or proton in the treatment of sinonasal cancer. IMRT and proton radiation therapy are the two most established and most commonly employed advanced radiotherapy techniques for the treatment of sinonasal cancer. It is highly controversial whether one is superior to the other in terms of local control and toxicity outcome. It is also not clear if a subset of patients would benefit more from one treatment technology versus the other. Due to the rarity and heterogeneity of sinonasal malignancies and the fact that proton beam is only available at a few centers in the United States, it is not feasible at present to do a Phase III study randomizing patients between IMRT and proton radiation therapy. In this study, a planned secondary analysis will be performed, comparing the treatment and toxicity outcome between IMRT and proton. The data on the IMRT and proton comparison from this trial will be used to design future multi-center prospective trials and to determine if randomized trial is necessary. In this study, the treatment technique employed for an individual case will not be determined by the treating physician(s), but rather by the most advanced technology available at the treating institution for the treatment of the sinonasal cancer. At the Massachusetts General Hospital (MGH), proton beam therapy will be used for patients who meet the eligibility criteria. For institutions where protons are not available or institutions where the proton planning systems have not been optimized, IMRT exclusively will be used for the treatment of sinonasal cancer. Patient and tumor characteristics are expected to be comparable between IMRT- and proton- institutions

NCT ID: NCT01586403 Active, not recruiting - Melanoma Clinical Trials

Transfer of Genetically Engineered Lymphocytes in Melanoma Patients

Start date: July 2012
Phase: Phase 1
Study type: Interventional

This is a phase one trial to determine if genetically engineered lymphocytes can be safely delivered to patients with metastatic melanoma.

NCT ID: NCT01556503 Active, not recruiting - Melanoma Clinical Trials

Sensitivity/Specificity Study of Non-invasive Imaging for Melanoma Diagnosis

Start date: April 2011
Phase: N/A
Study type: Observational

The purpose of this study is to show how well a new device, confocal microscope, works to detect malignant melanoma, a type of skin cancer.

NCT ID: NCT01551693 Active, not recruiting - Melanoma Clinical Trials

STA-9090(Ganetespib) in Patients With Unresectable Stage III or Stage IV Melanoma

Start date: September 2011
Phase: Phase 2
Study type: Interventional

STA9090 is a drug which inactivates or blocks the work of a protein called Heat Shock Protein 90 or HSP90. HSP90 is a protein that helps some molecules inside your cells to have the right shape. By stopping HSP90's activity, those molecules never get to have the right structure of be functional and they are destroyed. The investigators believe that if they stop the activity of HSP90, the rapidly dividing cells that are in your tumor(s) may slow down. In this research study the investigators are looking to see how well STA9090 works in stopping the spread of your melanoma.