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Neoplasms clinical trials

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NCT ID: NCT00560846 Terminated - Stomach Neoplasms Clinical Trials

Perioperative Nutrition in Upper Gastrointestinal (GI) Cancer Surgery

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

The aim of this study is to demonstrate the influence of peri-operative nutrition on the post-operative complications, preservation of lean body mass and length of stay after gastrectomy or oesophagectomy.

NCT ID: NCT00560716 Terminated - Solid Tumors Clinical Trials

A Phase I Pharmacologic Study of CYC116, an Oral Aurora Kinase Inhibitor, in Patients With Advanced Solid Tumors

Start date: June 2007
Phase: Phase 1
Study type: Interventional

This is a phase I study of an investigational cancer drug, CYC116, in patients with advanced solid tumors.

NCT ID: NCT00557206 Terminated - Neoplasms Clinical Trials

Oxaliplatin and Docetaxel for Recurrent or Metastatic Head and Neck Cancer

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

Patient receiving oxaliplatin and docetaxel will have longer progression free survival than those patients receiving standard care.

NCT ID: NCT00550654 Terminated - Ovarian Cancer Clinical Trials

Conformal Radiation Therapy in Treating Patients With Metastatic Cancer Outside the Brain

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

RATIONALE: Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. PURPOSE: This phase II trial is studying how well conformal radiation therapy works in treating patients with metastatic cancer outside the brain.

NCT ID: NCT00547261 Terminated - Neoplasms Clinical Trials

Phase I Dose Finding Study of SSR97225 Given in Patients With Refractory Cancer

Start date: October 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the maximally tolerated dose and the dose limiting toxicity of this antimitotic, tubulin binding investigational drug for those patients who have failed standard anticancer treatments.

NCT ID: NCT00532064 Terminated - Malignant Neoplasm Clinical Trials

Cardiac Biomarkers in Early Detection of Cardiotoxicity in Patients Receiving Sunitinib or Sorafenib Chemotherapy

Start date: September 12, 2007
Phase:
Study type: Observational

This trial studies how well cardiac biomarkers work in the early detection of cardiotoxicity in patients receiving sunitinib malate or sorafenib chemotherapy. Some chemotherapies are known to cause damage to heart muscle cells, resulting in heart failure. Often, the damage is not detected until heart failure has already occurred. Testing for cardiac biomarkers, such as troponin I and/or T and B-type natriuretic peptide (BNP), may be useful in detecting heart damage earlier than other tests currently performed (such as echocardiogram and electrocardiogram).

NCT ID: NCT00512798 Terminated - Melanoma Clinical Trials

Bortezomib and Temozolomide in Treating Patients With Advanced Refractory Solid Tumors or Melanoma

Start date: June 2003
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or stopping them from dividing. Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving temozolomide together with bortezomib may kill more tumor cells. PURPOSE: To determine the best dose of bortezomib and temozolomide and to see how well they work in treating patients with advanced refractory solid tumors or melanoma.

NCT ID: NCT00507702 Terminated - Neoplasms Clinical Trials

Identification of Key Blood Molecular Markers for Immunotherapy

Start date: July 6, 2006
Phase:
Study type: Observational

To identify unique blood markers in cancer patients so that we can identify patients with evidence of pre-existing immunity who may be a responder to immunotherapy.

NCT ID: NCT00506948 Terminated - Lymphoma Clinical Trials

Thymoglobulin, Sirolimus and Mycophenolate Mofetil for Prevention of Acute Graft-Versus-Host Disease (GVHD)

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

The goal of this clinical research study is to learn if the combination of rabbit anti-thymocyte globulin (Thymoglobulin®), sirolimus (Rapamune®), and mycophenolate mofetil (Cellcept®) can help to prevent graft versus host disease (GVHD). The safety of this drug combination will also be studied. Primary Objective: To determine efficacy and toxicity of a regimen of thymoglobulin, sirolimus and mycophenolate mofetil for prevention of acute GVHD after allogeneic stem cell transplantation from human leukocyte antigen (HLA) identical related or unrelated donors. Secondary Objective: To assess engraftment, chronic GVHD, relapse and survival.

NCT ID: NCT00503581 Terminated - Clinical trials for Stage 0 Uterine Corpus Cancer

Megestrol in Treating Patients With Endometrial Neoplasia or Endometrial Hyperplasia

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

This randomized phase II trial is studying how well megestrol works in treating patients with endometrial neoplasia or endometrial hyperplasia. Estrogen can cause the growth of endometrial cancer cells. Hormone therapy using megestrol may fight endometrial cancer by blocking the use of estrogen by the abnormal cells.