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Lymphoma clinical trials

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NCT ID: NCT00684411 Completed - Clinical trials for T Cell Non-Hodgkin Lymphoma

Gleevec in Relapsed/Refractory T Cell Non-Hodgkin's Lymphoma

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

The purpose of this research study is to evaluate the overall response rate to imatinib mesylate in participants with relapsed or refractory T cell non-Hodgkin's lymphoma. This drug has been used in chronic myeloid leukemia and information from those other research studies suggests that it may help to treat T cell non-Hodgkin's lymphoma.

NCT ID: NCT00683046 Completed - Clinical trials for Myelodysplastic Syndromes

T-Cell Depleted Allogeneic Stem Cell Transplantation for Patients With Hematologic Malignancies

Start date: November 2001
Phase: Phase 2
Study type: Interventional

Objectives: 1. To evaluate disease free survival after Campath 1H-based in vivo T-cell depletion and non-myelo-ablative ablative stem cell transplantation in patients with hematologic malignancies. 2. To evaluate the incidence and severity of acute and chronic GVHD after Campath 1H-based in vivo T-cell depletion, in patients with hematologic malignancies undergoing non-myelo-ablative stem cell transplantation. 3. To evaluate engraftment and chimerism after Campath 1H-based in vivo T-cell depletion and non-myelo-ablative ablative stem cell transplantation in patients with hematologic malignancies.

NCT ID: NCT00678327 Completed - Lymphoma Clinical Trials

Fludeoxyglucose F 18-PET/CT Imaging in Assessing Response to Chemotherapy in Patients With Newly Diagnosed Stage II, Stage III, or Stage IV Hodgkin Lymphoma

Start date: August 29, 2008
Phase: Phase 3
Study type: Interventional

RATIONALE: Imaging procedures, such as fludeoxyglucose F 18 (FDG)-PET/CT scan, done before, during, and after chemotherapy may help doctors assess a patient's response to treatment and help plan the best treatment. It is not yet known whether FDG-PET/CT imaging is effective in assessing response to chemotherapy in patients with newly diagnosed Hodgkin lymphoma. PURPOSE: This randomized phase III trial is studying FDG-PET/CT imaging to see how well it works in assessing response to chemotherapy in patients with newly diagnosed stage II, stage III, or stage IV Hodgkin lymphoma.

NCT ID: NCT00677105 Completed - Lymphoma Clinical Trials

A Safety and Dose-finding Study of JNJ-26481585 for Patients With Advanced Solid Malignancies and Lymphoma.

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

The purpose of this study is to assess the safety of the drug (JNJ-24681585 a drug in development for cancer) in patients with advanced or refractory solid malignancies or lymphoma on the maximum dose that can be tolerated by these patients. The absorption, breakdown and elimination of the drug will be studied and in some patients, the effect of the food on these processes will also be examined.

NCT ID: NCT00676806 Completed - Multiple Myeloma Clinical Trials

A Phase II Study of Umbilical Cord Blood Transplantation

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

This study is designed to determine whether Umbilical Cord Transplantation (UCB) can be substituted for adult bone marrow cells in the standard stem cell transplant regimens used at this hospital for subjects who do not have stem cell donors.

NCT ID: NCT00674024 Completed - Lymphoma Clinical Trials

Pazopanib to Treat Adults With Advanced Cancers and Varying Degrees of Liver Function

Start date: October 7, 2008
Phase: Phase 1
Study type: Interventional

Background: - Pazopanib is an experimental drug that was designed to enter cancer cells and block the activity of proteins that are important for cancer cell growth and survival. - This is the first study in which pazopanib is given to patients with different degrees of liver function. The safe dose for patients with normal liver function is already known. Objectives: - To determine the safety and side effects of pazopanib given at different dose levels to patients with cancer who have different degrees of liver function. - To find out how much pazopanib is in the blood at specific times. - To determine if pazopanib is effective in treating advanced cancer in patients with different degrees of liver function. Eligibility: - Patients 18 years of age and older with an advanced solid tumor or lymphoma that cannot be treated successfully with standard therapies and who have normal or abnormal liver function. Design: - Treatment: - Patients are divided into 4 groups, based on their liver function. The first three patients in each group receive a low dose of pazopanib. The next three in each group receive a higher dose of pazopanib if no serious side effects were reported in the previous three. The dose is increased in succeeding groups of three patients until the maximum study dose is reached. - Patients take pazopanib once a day by mouth in 21-day treatment cycles. Treatment continues until the cancer worsens, the patient develops severe side effects, the patient no longer wants to continue the study, or the doctor removes the patient from the study for other reasons. - Monitoring: - Blood pressure: Patients monitor and record their blood pressure twice a day after starting treatment. - Blood tests: Patients have weekly routine blood tests. In addition, at week 3 of the first cycle and again after the highest safe dose has been determined, several blood samples are collected at frequent intervals to determine how the body handles the drug. - Imaging studies: X-rays or scans or both are done to measure the extent of disease every 3 cycles. - Physical examinations are done at periodic intervals.

NCT ID: NCT00671112 Terminated - Lymphoma Clinical Trials

Everolimus and Bortezomib in Treating Patients With Relapsed or Refractory Lymphoma

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

RATIONALE: Everolimus and bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. PURPOSE: This phase I trial is studying the side effects and best dose of everolimus when given together with bortezomib in treating patients with relapsed or refractory lymphoma.

NCT ID: NCT00670592 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Study of HCD122 in Adults With Non-Hodgkin's or Hodgkin's Lymphoma Who Have Progressed After at Least Two Prior Therapies

Start date: March 2008
Phase: Phase 1/Phase 2
Study type: Interventional

This study is to evaluate the highest tolerated dose, safety and activity of HCD122 in adults with non-Hodgkin's or Hodgkin's lymphoma who have received at least two prior therapies.

NCT ID: NCT00670358 Active, not recruiting - Lymphoma Clinical Trials

Lenalidomide, Rituximab, and Combination Chemotherapy in Treating Patients With Newly Diagnosed Stage II, Stage III, or Stage IV Diffuse Large Cell or Follicular B-Cell Lymphoma

Start date: August 25, 2008
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Lenalidomide may stimulate the immune system in different ways and stop cancer cells from growing. Monoclonal antibodies, such as rituximab, 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. Drugs used in chemotherapy, such as cyclophosphamide, doxorubicin, vincristine, and prednisone, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving lenalidomide together with rituximab and combination chemotherapy may kill more cancer cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of lenalidomide when given together with rituximab and combination chemotherapy and to see how well they work in treating patients with newly diagnosed stage II, stage III, or stage IV diffuse large cell or follicular B-cell lymphoma.

NCT ID: NCT00669877 Completed - Burkitt's Lymphoma Clinical Trials

Rituximab and Hyper-CVAD (Cyclophosphamide, Vincristine, Adriamycin, and Dexamethasone) for Burkitt's and Burkitt's -Like Leukemia/Lymphoma

Start date: August 2002
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if intensive chemotherapy given over 6 months can help to control or cure Burkitt's leukemia, Burkitt's lymphoma, or small non-cleaved cell B-cell leukemia or lymphoma. Another goal is to see how well this treatment works when given with Rituximab. The safety of the combined treatment will also be studied.