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Melanoma clinical trials

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NCT ID: NCT00818480 Completed - Prostate Cancer Clinical Trials

An Extension Study Administering YM155 to Subjects Previously Enrolled in Another Protocol Administering YM155

Start date: February 2006
Phase: Phase 2
Study type: Interventional

This protocol is open to subjects previously enrolled in and who had completed a Phase I or Phase II study administering YM155. Subjects who are receiving benefit from treatment with YM155 are eligible after completing the previous study.

NCT ID: NCT00816374 Completed - Melanoma Clinical Trials

Tailored Intervention for Melanoma Patient's Families

Start date: August 2005
Phase: N/A
Study type: Interventional

The purpose of the investigators' study is to find the best way to provide information about sun protection and skin cancer detection. The investigators want to see which of two methods most improves sun protection and screening attitudes and practices. The investigators hope to improve these attitudes and practices among people who are at higher risk for melanoma. People at higher risk for melanoma are first degree relatives (mother, father, sibling or child) of people diagnosed with melanoma.

NCT ID: NCT00815607 Completed - Melanoma Clinical Trials

Trial of an Intratumoral Injections of INXN-3001 in Subjects With Stage III or IV Melanoma

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

The purpose of this study is to test the safety of an investigational combination drug/immunotherapy for the treatment of Stage III/IV melanoma.

NCT ID: NCT00804908 Completed - Melanoma Clinical Trials

A Study Evaluating Efficacy of ABT-888 in Combination With Temozolomide in Metastatic Melanoma

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

The purpose of this study is to evaluate the efficacy of ABT-888 in combination with temozolomide versus temozolomide alone in subjects with metastatic melanoma.

NCT ID: NCT00798629 Completed - Melanoma (Skin) Clinical Trials

Adenovirus CCL-21 Transduced MART-1/gp100/Tyrosinase/NY-ESO-1 Peptide-Pulsed Dendritic Cells Matured

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

RATIONALE: Vaccines made from gene-modified tumor cells may help the body build an immune response to kill tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of vaccine therapy in treating patients with metastatic melanoma.

NCT ID: NCT00796991 Completed - Advanced Melanoma Clinical Trials

Drug-Drug Interaction - 3 Arm - Carboplatin/Paclitaxel, Dacarbazine

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

The purpose of this clinical research study is to learn the pharmacokinetics of Ipilimumab when combined with Paclitaxel/Carboplatin or Dacarbazine

NCT ID: NCT00794235 Completed - Clinical trials for Melanoma Stage III or IV

Monocentric Pilot Study Investigating the Metabolic Activity of Melanoma in Vivo During Sorafenib and Dacarbazine

Start date: December 2008
Phase: Phase 2
Study type: Interventional

Investigation of the metabolic activity of sorafenib and sorafenib plus dacarbazine on melanoma metastasis in patients with melanoma stage III or IV on the basis of PET/CT, LDH and S-100 evaluation. As we hypothezise a direct influence on the transcriptome by these drugs via antiproliferative or apoptotic signals, biopsies of melanoma skin metastases will be assessed with microarrays and direct changes will be revealed. If positive effects on the transcriptional profiles of metastases are revealed, patients with metastatic melanomas would benefit from these drugs resulting in tumor regressions. Therefore, a total of 12 patients with skin- or superficial lymph node metastases with a diameter of at least 1 cm will be chosen for sorafenib therapy over 56 days per os twice daily with each 400 mg and, additionally, on day 14 and 42, intravenous dacarbazine infusion (volume depending on the body surface area (1000 mg/m2)). Before treatment with sorafenib, before treatment with dacarbazine, and after treatment, S100 and LDH will be measured in serum, PET/CT will be conducted and biopsy will be taken out of one skin metastasis on the same day.

NCT ID: NCT00790010 Completed - Melanoma Clinical Trials

Bevacizumab Plus Ipilimumab in Patients With Unresectable Stage III or IV Melanoma

Start date: February 26, 2009
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to determine the safety of using the study drugs bevacizumab and ipilimumab together, and the doses in combination which can be given to people safely. This study also seeks to investigate whether using both study drugs lengthens the amount of time before the participants melanoma worsens.

NCT ID: NCT00788775 Completed - Melanoma Clinical Trials

Nilotinib in TKI Resistant or Intolerant Patients With Metastatic Mucosal, Acral, or Chronically Sun Damaged Melanoma

Start date: January 23, 2009
Phase: Phase 2
Study type: Interventional

Given the poor prognosis and limited treatment options available for patients with mucosal or acral/lentiginous melanomas who develop metastatic disease, genetic discoveries of KIT mutations in these cancers present the need to test multi-targeted kinase inhibitors with potent KIT inhibitory activity in this patient population. Imatinib and other tyrosine kinase inhibitors (TKIs) have the potential to be effective in this patient population, but patients may develop resistance to treatment. Therefore, in this study, we propose to test nilotinib in patients with metastatic mucosal, acral, or chronically sun-damaged melanoma following treatment with another TKI.

NCT ID: NCT00785369 Completed - Melanoma Clinical Trials

In Vivo Confocal Microscopy for Pigmented Lesion Diagnosis

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

The purpose of this study is to image pigmented skin lesions suspicious for melanoma with an imaging technology called in vivo reflectance confocal microscopy. This technology uses low intensity laser to image below the surface of the skin. The confocal images of the suspicious skin lesion will be examined. The goal of this study is to compare the results of the confocal image examination to the pathologic diagnosis of the skin lesion. The technique being evaluated in this study uses reflectance confocal microscopy in vivo. The term "in vivo" means in/on a living subject. In this study you will be the living subject and the confocal microscope will be placed on your skin to look at your skin lesion. The confocal microscope uses a weak laser light and a sophisticated lens to image the individual cells that make up the skin. Your lesion will be photographed with high resolution photography.