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Neoplasms clinical trials

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NCT ID: NCT00611793 Completed - Clinical trials for Advanced Malignancies

PTK787/ZK222584 With Bevacizumab in Patients With Refractory and/or Advanced Malignancies

Start date: October 2004
Phase: Phase 1
Study type: Interventional

PTK787/ZK222584 is an orally active inhibitor of VEGF-R tyrosine kinases. Bevacizumab is an intravenous humanized monoclonal antibody directed against vascular endothelial growth factor. By binding to VEGF, bevacizumab blocks VEGF-A receptor binding. Due to the different mechanisms of action and the non-overlapping toxicity profiles of the two agents, it is hoped that a combination regimen incorporating both compounds will produce increased activity without enhanced toxicity.

NCT ID: NCT00610194 Completed - Advanced Cancer Clinical Trials

Phase 1 Dose-escalation PK/PD Trial in Advanced Cancer Patients

Start date: November 28, 2007
Phase: Phase 1
Study type: Interventional

Primary Objective: To evaluate the safety of escalating oral doses of RDEA119, a MEK inhibitor, in advanced cancer patients. Secondary Objectives: - To describe the initial PK of different doses of RDEA119 when given once orally on Day 1 of the study - To describe the PK of different doses of RDEA119 when given orally as continuous dosing. - To examine the inhibition of MEK products (p-ERK), cytokine products, and other protein biomarkers - To expand the MTD dose cohort to evaluate the safety, tolerability and PK/PD of the recommended Phase 2 dose - To explore the presence of genotype, PD markers, cell growth and a marker of apoptosis, in paired tumor biopsy samples of patients' tumors pre-dose and during dosing in a minimum of 10 patients in the expanded cohort

NCT ID: NCT00610129 Completed - Clinical trials for Neuroendocrine Tumors

Clinical and Translational Study of MK-0646 in Patients With Metastatic Neuroendocrine Tumors (NET)

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

The purpose of this study is to test a new drug for neuroendocrine tumors. We think that this new drug may help control your tumor. MK-0646 is a monoclonal antibody. An antibody is a protein that is able to attach to specific target on cancer cells. This target helps the cancer cells grow and divide. By attaching to the target, it may stop the cancer cells from further growth and dividing. This study will help find out if MK-0646 is a helpful drug when taken in patients with neuroendocrine tumor. This study is a phase 2 study. The purpose of a phase 2 study is to find out what effects, good and/or bad, MK-0646 has on metastatic neuroendocrine tumors.

NCT ID: NCT00609141 Completed - Clinical trials for Unspecified Childhood Solid Tumor, Protocol Specific

IMC-A12 in Treating Young Patients With Relapsed or Refractory Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor or Other Solid Tumor

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

This phase I clinical trial is studying the side effects and best dose of IMC-A12 in treating young patients with relapsed or refractory Ewing sarcoma/peripheral primitive neuroectodermal tumor or other solid tumors. Monoclonal antibodies, such as IMC-A12, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them.

NCT ID: NCT00608933 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Education Intervention in Encouraging Health Providers to Talk With Cancer Patients About the Use of Complementary and Alternative Medicine

Start date: June 2008
Phase: Phase 3
Study type: Interventional

RATIONALE: Educating health providers on talking with cancer patients about complementary and alternative medicine (CAM) may help encourage health providers to talk more often with cancer patients about the use of CAM. PURPOSE: This randomized phase III trial is studying how well an education intervention works in encouraging health providers to talk with cancer patients about the use of CAM.

NCT ID: NCT00607984 Recruiting - Tumors Clinical Trials

Administration of High Dose Thiotepa and Melphalan With Autologous Hematopoietic Stem Cell Transplant in Children and Adolescents With Solid Tumors

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

The prognosis of children and adolescents with high risk tumors of the central nervous system and other miscellaneous solid tumors is poor despite modern treatment protocols. Frequently, physicians suggest additional therapy with high dose chemotherapy after a good initial response to standard doses of treatment has been obtained, so as to reduce the chance that the tumor will recur. We propose a regimen of high dose thiotepa and melphalan followed by rescue of the patient's previously stored hematopoietic (blood manufacturing) system with blood stem cells. The aim of this study is to prove that this therapy is tolerable in children and adolescents, that it results in tolerable levels of toxicity, and that it improves the survival of this group of children as compared to standard therapy given in the past

NCT ID: NCT00607802 Withdrawn - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Donor White Blood Cell Infusion in Treating Patients With Metastatic or Unresectable Cancer

Start date: n/a
Phase: N/A
Study type: Interventional

RATIONALE: White blood cells from donors may be able to kill cancer cells in patients with cancer. PURPOSE: This clinical trial is studying the side effects of donor white blood cell infusion in treating patients with metastatic or unresectable cancer.

NCT ID: NCT00607399 Terminated - Advanced Cancer Clinical Trials

Safety Study of SGX523, a Small Molecule Met Inhibitor, to Treat Solid Tumors

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

SGX523 is a drug which acts by blocking the function of an enzyme called MET. MET activity may be important in growth and survival of some types of cancer. This Phase I trial is studying the safety, side effects, and best dose of SGX523 when given to patients with advanced cancer, and how well it inhibits MET activity in tumors.

NCT ID: NCT00607048 Completed - Neoplasms Clinical Trials

Dose Finding Study Of CP-870,893, An Immune System Stimulating Antibody, In Combination With Paclitaxel And Carboplatin For Patients With Metastatic Solid Tumors

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

This is a dose-finding study; therefore, there is no hypothesis testing

NCT ID: NCT00606879 Terminated - Advanced Cancer Clinical Trials

Safety Study of SGX523, a Small Molecule Met Inhibitor, to Treat Solid Tumors

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

SGX523 is a drug which acts by blocking the function of an enzyme called MET. MET activity may be important in growth and survival of some types of cancer. This Phase I trial is studying the safety, side effects, and best dose of SGX523 when given to patients with advanced cancer, and how well it inhibits MET activity in tumors.