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Neoplasms clinical trials

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NCT ID: NCT00890747 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Sunitinib Malate in Treating HIV-Positive Patients With Cancer Receiving Antiretroviral Therapy

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

This phase I trial studies the side effects and the best dose of sunitinib malate in treating human immunodeficiency virus (HIV)-positive patients with cancer receiving antiretroviral therapy. Sunitinib malate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.

NCT ID: NCT00890500 Completed - Clinical trials for Hematologic Malignancies

Safety and Efficacy of ProHema Modulated Umbilical Cord Blood Units in Subjects With Hematologic Malignancies.

Start date: January 2011
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to determine the safety and efficacy of a reduced intensity conditioning regimen during a double umbilical cord blood unit transplant with one of the cord blood units modulated with ProHema.

NCT ID: NCT00889954 Completed - Clinical trials for HER2 Positive Malignancies

Her2 and TGFBeta Cytotoxic T Cells in Treatment of Her2 Positive Malignancy

HERCREEM
Start date: May 2009
Phase: Phase 1
Study type: Interventional

Patients have advanced stage cancer. This study is a gene transfer research study using special immune cells. The body has different ways of fighting infection and disease. No single way seems perfect for fighting cancers. This research study combines two different ways of fighting cancer: antibodies and T cells. Investigators hope that both will work better together. Antibodies are proteins that protect the body from diseases caused from infectious diseases and possibly cancer. T cells, also called T lymphocytes, are special infection-fighting blood cells that can kill other cells, including tumor cells or cells that are infected with germs. Both antibodies and T cells have been used to treat patients with cancers: they both have shown promise, but have not been strong enough to cure most patients. T lymphocytes can kill tumor cells but there are normally not enough of them or they are not able to kill all the tumor cells. We have done research in which we have grown "extra" T lymphocytes. We have added genes to those T lymphocytes to help them to recognize tumor cells. Although the results have been promising, we are still doing more research in this area. Antibodies usually circulate in blood and are secreted by other cells of the immune system in response to the presence of germs or abnormal cells in the body. The antibody used in this study is called anti-HER2 (Human Epidermal Growth Factor Receptor 2). This antibody sticks to HER2-positive cancer cells because of a substance on the outside of these cells called HER2.

NCT ID: NCT00886522 Completed - Clinical trials for Hematological Malignancies

Intrabone Infusion of Cord Blood in Adults With Hematological Malignancies

IBCB
Start date: April 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the engraftment of donor hemopoiesis (proportion of transplanted patients with successful engraftment at day +42) in adult patients affected by high risk hematological malignancies after intrabone infusion of cord blood.

NCT ID: NCT00884845 Completed - Clinical trials for Advanced Malignant Solid Tumors

Trial of PM02734 Administered in Combination With Erlotinib in Patients With Advanced Malignant Solid Tumors

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

Phase I multicenter, open-label, dose-escalating clinical and pharmacokinetic trial of PM02734 administered in combination with erlotinib to determine the safety and tolerability and to identify the dose limiting toxicity (DLT) and the recommended dose (RD) of the combination of PM02734 and erlotinib, in patients with advanced malignant solid tumors.

NCT ID: NCT00884364 Recruiting - Clinical trials for Hematological Malignancies

Exercise During Chemotherapy for Patients With Hematological Malignancies

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The trial will evaluate the effects of aerobic exercise in patients undergoing chemotherapy for the treatment of a hematological neoplastic disease.

NCT ID: NCT00881946 Completed - Clinical trials for Hematologic Malignancies

Repeat Dose Safety Study for Compound to Treat Hematologic Cancer

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

The purpose of this study is to characterize the safety and tolerability of repeat doses of compound GSK2110183 in subjects with hematologic cancer.

NCT ID: NCT00880633 Completed - Clinical trials for Periampullary Neoplasms

Endoscopic Ultrasound Staging of Periampullary Neoplasms: Retrospective

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

The purpose of this retrospective study is to determine the degree to which a biliary stent affects EUS staging accuracy of ampullary tumors.

NCT ID: NCT00880568 Completed - Neoplasms Clinical Trials

Phase I Study of MK-1496 in Patients With Advanced Solid Tumor (MK-1496-002 AM 4)(COMPLETED)

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

This study determines recommended clinical dose, to evaluate the safety, tolerability and pharmacokinetics of MK-1496 in patients with locally advanced and/or metastatic solid tumors who have failed standard therapy or for whom no standard therapy exists, in two dosing schedules in Japan.

NCT ID: NCT00880074 Completed - Malignant Neoplasm Clinical Trials

FLT-PET in Predicting Response to Chemotherapy in Patients With Advanced Malignancies

Start date: April 9, 2009
Phase: Phase 1
Study type: Interventional

This clinical trial studies fluorine F-18 fluorothymidine (FLT)-positron emission tomography (PET) in predicting response to chemotherapy in patients with advanced malignancies. FLT solution can help locate cancer cells inside the body. Diagnostic procedures, such as FLT-PET, may help find tumors and measure a patient's response to treatment.