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Uveal Melanoma clinical trials

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NCT ID: NCT01955941 Completed - Uveal Melanoma Clinical Trials

Vascular Response to Brachytherapy Using Functional OCT

Start date: October 2013
Phase:
Study type: Observational

The purpose of this study is to learn how blood flows to tumors in patients treated with I-125 plaque brachytherapy for uveal melanoma.

NCT ID: NCT01924923 Completed - Uveal Melanoma Clinical Trials

New Biopsy Technique for Uveal Melanoma

Start date: June 2013
Phase: N/A
Study type: Observational

This pilot study intends to investigate a new biopsy technique that will decrease the incidence of tumor cells in the biopsy tract.

NCT ID: NCT01430416 Completed - Uveal Melanoma Clinical Trials

Safety and Efficacy of AEB071 in Metastatic Uveal Melanoma Patients

Start date: December 20, 2011
Phase: Phase 1
Study type: Interventional

This study has two parts, dose escalation and dose expansion. For dose escalation, the primary objective is to estimate the maximum tolerated dose (MTD) of AEB071 in patients with uveal melanoma. For dose expansion, the primary objective is to characterize the safety and tolerability of the MTD of AEB071 in patients with uveal melanoma.

NCT ID: NCT01338389 Completed - Uveal Melanoma Clinical Trials

Influence of Oral Treatment With Citicoline for the Prevention of Radiation Optic Neuropathy in Patients Treated for Uveal Melanomas With Proton Beam Therapy

Start date: June 25, 2012
Phase: N/A
Study type: Interventional

Proton beam irradiation is the treatment of choice for uveal melanomas. It has favorable results in causing tumor regression while preserving the eye. Optic neuropathy has emerged consistently as an irreversible cause of visual loss in proton beam irradiated eyes. No neuroprotective strategies are available at present. Citicoline is a choline agent precursor available as a dietary supplement. Citicoline conferred acute neuroprotection and enhanced neuroplasticity in experimental stroke models. In ophthalmology, citicoline has demonstrated a significant action in improving retinal and cortical responses in patients with optic nerve diseases (glaucoma, ischemic optic neuropathy). Citicoline also exhibits a very low toxicity profile in humans. The purpose of the study is to demonstrate whether daily oral administration of citicoline in patients treated for uveal melanomas with proton beam therapy, prevents or delays the occurrence of radiation optic neuropathy. Changes in visual acuity, Pattern ERG and visual evoked potentials are measured. The tolerability/safety of the product is also evaluated.

NCT ID: NCT01252251 Completed - Uveal Melanoma Clinical Trials

RAD001 (Everolimus) and Pasireotide (SOM230) LAR in Patients With Advanced Uveal Melanoma

Start date: November 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to find out what effects, good and/or bad, the drugs everolimus and pasireotide have on the patient and on melanoma. Pasireotide is also called SOM-230. Pasireotide is an experimental drug and is not approved by the Food and Drug Administration. Everolimus is also called RAD001. Everolimus is approved for use in the U.S. for kidney cancer. Everolimus is not approved for treatment of melanomas, but early studies show that it may help some patients with melanoma.

NCT ID: NCT01034787 Completed - Uveal Melanoma Clinical Trials

Study of AntiCTLA4 in Patients With Unresectable or Metastatic Uveal Melanoma

Start date: August 17, 2009
Phase: Phase 2
Study type: Interventional

This is a Phase 2, multi-center, open-label study in patients with surgically incurable stage III or IV uveal melanoma who have not received prior immunotherapy. CP-675,206 is thought to stimulate patients' immune systems to attack their tumors. CP-675,206 has been shown to induce durable tumor responses in patients with metastatic melanoma in phase 1 and phase 2 clinical studies.

NCT ID: NCT00661622 Completed - Liver Metastases Clinical Trials

Halt Growth of Liver Tumors From Uveal Melanoma With Closure of Liver Artery Following Injection of GM-CSF

Start date: October 2004
Phase: Phase 2
Study type: Interventional

Patients with uveal melanoma metastatic to the liver will be treated with embolization of the hepatic artery every 4 weeks. GM-CSF (granulocyte-macrophage colony simulating factor) or normal saline will be injected into one of the liver arteries with an oily contrast dye, Ethiodol. This is followed by blockage of the artery with small pieces of gelatin sponge (embolization). It is hoped with this novel approach that: - tumor cells will die due to a loss of their blood supply, - local inflammatory reactions induced by GM-CSF will kill remaining tumor cells, and - a systemic immune response against tumor cells may develop.

NCT ID: NCT00596362 Completed - Uveal Melanoma Clinical Trials

Treatment With Intravitreal Avastin for Large Uveal Melanomas

Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to test the safety and effectiveness of Avastin introduced into the inside of the eyeball in causing shrinkage of the uveal melanoma (tumor of the eye). Avastin is an anti-cancer drug specially designed to shrink blood vessels within tumors.

NCT ID: NCT00351728 Completed - Uveal Melanoma Clinical Trials

Combined PET/CT Imaging for the Early Detection of Ocular Melanoma Metastasis Compared to CT Scanning Alone

Start date: June 2006
Phase: N/A
Study type: Observational

Patients diagnosed with ocular melanoma consent to participate in the study. Combined PET/CT scans of the whole body are performed at baseline, three months later, and six months after that for a total of three combined scans in the first year. Subsequently, these combined scans will be performed at 6-monthly intervals for a total of two combined scans per year.

NCT ID: NCT00121225 Completed - Stage IV Melanoma Clinical Trials

Vorinostat in Treating Patients With Metastatic or Unresectable Melanoma

Start date: September 2005
Phase: Phase 2
Study type: Interventional

This phase II trial is studying how well vorinostat works in treating patients with metastatic or unresectable melanoma. Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.