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Lymphoma, Non-Hodgkin clinical trials

View clinical trials related to Lymphoma, Non-Hodgkin.

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NCT ID: NCT00049439 Completed - Lymphoma Clinical Trials

Combination Chemotherapy in Treating Patients With AIDS-Related Non-Hodgkin's Lymphoma

Start date: March 1998
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of combining lomustine, etoposide, cyclophosphamide, and procarbazine in treating patients who have AIDS-related non-Hodgkin's lymphoma.

NCT ID: NCT00049036 Completed - Clinical trials for AIDS-related Peripheral/Systemic Lymphoma

Combination Chemotherapy and Rituximab in Treating Patients With HIV-Associated Stage I, Stage II, Stage III, or Stage IV Non-Hodgkin's Lymphoma

Start date: March 2003
Phase: Phase 2
Study type: Interventional

This randomized phase II trial is studying how well giving combination chemotherapy together with rituximab works in treating patients with HIV-associated stage I, stage II, stage III, or stage IV non-Hodgkin's lymphoma. Drugs used in chemotherapy work in different ways to stop cancer cells from dividing so they stop growing or die. Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Combining chemotherapy with monoclonal antibody therapy may kill more cancer cells.

NCT ID: NCT00048555 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Safety and Efficacy of IDEC-114 in Combination With Rituxan in the Treatment of Non-Hodgkin's Lymphoma

Start date: November 2002
Phase: Phase 1/Phase 2
Study type: Interventional

To determine what side effects and what clinical effect, if any, the administration of this investigational product, IDEC-114 in combination with Rituxan® [Rituxan® as a single agent is approved by the United States Food and Drug Administration (FDA) to treat patients with relapsed or refractory follicular NHL], has in this patient population.

NCT ID: NCT00045877 Completed - Clinical trials for Lymphoma, Non-Hodgkin

Proleukin in Combination With Rituxan in Patients With Low-Grade Non-Hodgkin's Lymphoma Who Have Previously Failed Rituxan Treatments

Start date: n/a
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine the safety and effectiveness of combination therapy with Proleukin and Rituxan on patients with low-grade Non-Hodgkin's Lymphoma who have previously failed Rituxan treatments.

NCT ID: NCT00045864 Completed - Clinical trials for Lymphoma, Non-Hodgkin

Proleukin in Combination With Rituxan in Patients With Intermediate and High-Grade Non-Hodgkin's Lymphoma.

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and effectiveness of combination therapy with Proleukin and Rituxan on patients with intermediate-and high- grade Non-Hodgkin's lymphoma.

NCT ID: NCT00044902 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Monoclonal Antibody Treatment for Non-Hodgkin's Lymphoma (Low-Grade)

Start date: n/a
Phase: Phase 2
Study type: Interventional

Epratuzumab is currently being studied in combination with rituximab, for the treatment of patients with low-grade NHL who failed previous chemotherapy and have never received rituximab or who received rituximab as a single agent or in combination with chemotherapy as their last treatment and who demonstrated a partial response or complete response for at least 12 months.

NCT ID: NCT00044551 Completed - Clinical trials for Lymphoma, Non-Hodgkin

Evaluation of Bay 59-8862 in Patients With Aggressive, Refractory Non-Hodgkin's Lymphoma

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

Almost two-thirds of lymphoma cases are Non-Hodgkin's Lymphomas (NHL). NHL is a malignant process that affects lymphoid cells found both in the lymph nodes and extranodally. Incidence and mortality rates from NHL are highest in developed countries. While many patients with aggressive NHL are curable with initial anthracycline-containing regimens, the majority of patients will relapse or prove refractory to initial therapy. The prognosis of patients with disease recurrence following a multidrug regimen is also limited. The current protocol is designed to test the safety and efficacy of BAY 59-8862 in patients with Aggressive Refractory Non-Hodgkin's Lymphoma.

NCT ID: NCT00043459 Terminated - Clinical trials for Non-Hodgkin's Lymphoma

Study of T900607-Sodium in Previously Treated Patients With Non-Hodgkin's Lymphoma.

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

The purpose of the study is to determine whether T900607-sodium is effective and safe in treating non-Hodgkin's lymphoma.

NCT ID: NCT00042913 Active, not recruiting - Lymphoma Clinical Trials

Epratuzumab in Treating Patients With Non-Hodgkin's Lymphoma

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

RATIONALE: Monoclonal antibodies such as epratuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. PURPOSE: Randomized phase II trial to study the effectiveness of epratuzumab in treating patients who have non-Hodgkin's lymphoma.

NCT ID: NCT00041730 Active, not recruiting - Clinical trials for Non-Hodgkin's Lymphoma

Rituxan Plus FavId (Idiotype Vaccine) for Low-grade Non-Hodgkin's Lymphoma

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

The purpose of this study is to evaluate the ability of patients treated with Rituxan® plus FavId™ and GM-CSF to mount an immune response (humoral and/or cellular) to KLH and their idiotype.