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Lymphoma clinical trials

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NCT ID: NCT00359086 Completed - Lymphoma Clinical Trials

Study of MGCD0103 Given Three Times Weekly in Patients With Relapsed and Refractory Lymphoma

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

In this study, MGCD0103, a new anticancer drug under investigation, is given three times weekly to patients with relapsed and refractory lymphoma.

NCT ID: NCT00357500 Completed - Lymphoma Clinical Trials

Etoposide, Cyclophosphamide, Thalidomide, Celecoxib, and Fenofibrate in Relapsed or Progressive Cancer

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

RATIONALE: Drugs used in chemotherapy, such as etoposide and cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Thalidomide, celecoxib, and fenofibrate may stop the growth of cancer cells by blocking blood flow to the cancer. Celecoxib also may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving combination chemotherapy together with thalidomide, celecoxib, and fenofibrate may kill more cancer cells. PURPOSE: This phase II trial is studying how well giving etoposide and cyclophosphamide together with thalidomide, celecoxib, and fenofibrate works in treating young patients with relapsed or progressive cancer.

NCT ID: NCT00355472 Completed - Clinical trials for Adult T-Cell Leukemia and Lymphoma (ATL)

Phase I Study of KW-0761 in Relapsed Patients With CCR4-Positive ATL and PTCL

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

This is a Phase I label dose escalation study of KW-0761 in relapsed patients with CCR4 positive Adult T-Cell Leukemia-Lymphoma (ATL) and Peripheral T-Cell lymphoma (PTCL).

NCT ID: NCT00355199 Completed - Clinical trials for Diffuse Large B-Cell Lymphoma

Comparison of HD Chemotherapy Followed by Auto-transplant and R-CHOP in High Risk Patients With DLBCL.

Start date: May 2005
Phase: Phase 3
Study type: Interventional

Multicentric randomized phase III study comparing high doses of chemotherapy with Rituximab followed by auto-transplant HPC versus CHOP plus Rituximab as first line therapy in high risk patients with DLBCL Non-Hodgkin's lymphomas.

NCT ID: NCT00354926 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Safety and Efficacy Study of an Anti-CD20 Monoclonal Antibody (AME-133v) to Treat Non-Hodgkin's Lymphoma

Start date: July 2006
Phase: Phase 1
Study type: Interventional

This study is designed to provide evidence of the safety and a preliminary understanding of the efficacy of AME 133v.

NCT ID: NCT00352846 Completed - Lymphoma Clinical Trials

Effect of Zoledronic Acid on Chemotherapy Induced Bone Loss

Start date: January 2006
Phase: Phase 3
Study type: Interventional

Primary Objective: - Evaluate the effect of zoledronate on change in bone mineral density (BMD) at the total lumbar spine and femoral neck. Secondary Objectives: - Evaluate the effect of zoledronate on change in BMD at the total hip - Evaluate risk factors for developing osteoporosis on chemotherapy - Determine correlative markers for response to zoledronate 4. Evaluate zoledronate effect on new bone fractures 5. Evaluate the cost-effectiveness of zoledronic acid (with calcium and vitamin D) versus standard treatment (calcium and vitamin D alone).

NCT ID: NCT00352443 Completed - Lymphoma Clinical Trials

S0528 Lapatinib and Everolimus in Treating Patients With Advanced Solid Tumors or Non-Hodgkin's Lymphoma

Start date: September 2006
Phase: Phase 1
Study type: Interventional

RATIONALE: Lapatinib and everolimus may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Everolimus may also stop the growth of cancer cells by blocking blood flow to the cancer. Giving lapatinib together with everolimus may kill more cancer cells. PURPOSE: This phase I trial is studying the side effects and best dose of lapatinib and everolimus in treating patients with advanced solid tumors or non-Hodgkin's lymphoma.

NCT ID: NCT00352027 Completed - Hodgkin's Lymphoma Clinical Trials

Chemotherapy With Low-Dose Radiation for Pediatric Hodgkin Lymphoma

Start date: July 20, 2006
Phase: Phase 2
Study type: Interventional

The main purpose of this protocol is to estimate the percentage of patients with intermediate risk Hodgkin lymphoma who will survive free of disease (Event-free survival) for three years after treatment with multi-agent chemotherapy (Stanford V) and low-dose, tailored-field radiation therapy. The hypothesis being studied is that this treatment will result in more than 80% of patients being alive and free of disease three years after starting treatment.

NCT ID: NCT00348985 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

PXD101 and Bortezomib in Treating Patients With Advanced Solid Tumors or Lymphomas

Start date: March 2006
Phase: Phase 1
Study type: Interventional

This phase I trial is studying the side effects and best dose of PXD101 and bortezomib in treating patients with advanced solid tumors or lymphomas. PXD101 and bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. PXD101 may also cause cancer cells to look more like normal cells, and to grow and spread more slowly. Giving PXD101 together with bortezomib may kill more cancer cells.

NCT ID: NCT00347971 Completed - Clinical trials for Lymphoma, Non-Hodgkin

Study of Recombinant Interleukin 21 in Combination With Rituxan for Non-Hodgkin's Lymphoma

Start date: June 2006
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate whether recombinant IL-21 used in combination with rituximab is safe for patients with non-Hodgkin's lymphoma (NHL).