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Lymphoplasmacytic Lymphoma clinical trials

View clinical trials related to Lymphoplasmacytic Lymphoma.

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NCT ID: NCT00644189 Completed - Clinical trials for Mantle Cell Lymphoma

Oral Clofarabine for Relapsed/Refractory Non-Hodgkin Lymphoma

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

Oral clofarabine is related to two intravenous chemotherapy drugs used for this disease and works in two different ways. It affects the development of new cancer cells by blocking two enzymes that cancer cells need to reproduce. When these enzymes are blocked, the cancer call can no longer prepare the DNA needed to make new cells. Clofarabine also encourages existing cancer cells to die by disturbing components within the cancer cell. This causes the release of a substance that is fatal to the cell. This trial studies the efficacy of oral clofarabine in the treatment of relapsed non-Hodgkin lymphomas.

NCT ID: NCT00566332 Completed - Clinical trials for Splenic Marginal Zone Lymphoma

Trial Comparing Chlorambucil to Fludarabine in Patients With Advanced Waldenström Macroglobulinemia

Start date: June 2001
Phase: Phase 3
Study type: Interventional

Waldenström's macroglobulinaemia (WM) is a lymphoproliferative disorder characterized by a monoclonal IgM paraprotein and morphological evidence of lymphoplasmacytic lymphoma: the cells are IgM+, IgD+, CD19+ and CD20+ but usually CD5-, CD10- and CD23-. The treatment efficacy is difficult to assess because of the lack of clear diagnostic criteria , good response criteria, and of randomized trials. The actual treatment is Chlorambucil, an alkylating agent. A purine analogue such as Fludarabine has proven its efficacy on 30 % to 80 % as first line therapy This study is a phase II b open, prospective, international multicenter trial (England, Dr Johnson, Dr Catovsky, Australia: Dr Seymour) promoted by the French Cooperative Group on Chronic Lymphoid Leukemia in untreated WM, or closely related disorders ( Lymphoplasmacytic lymphoma or splenic marginal zone lymphoma). 366 patients must be included, among them 180 patients in France. Patients will be stratified according to the lymphoproliferative disorder. The patients will receive Chlorambucil by oral route for 10 days every 28 days (12 cycles) (8 MG/M², 6 MG/M² if patient is more than 75 years old) or Fludarabine by oral route for 5 days every 28 days (6 cycles) (40MG/M², 30 MG/M² if patient is more than 75 years old). The primary objective is to compare the efficacy (response rate) of Chlorambucil to Fludarabine in previously untreated patients. The secondary objectives are the duration of response, the improvement of hematological parameters, the toxicity, the quality of life, the event free survival and the overall survival.

NCT ID: NCT00142181 Completed - Clinical trials for Lymphoplasmacytic Lymphoma

Phase II Study of Campath-1H Antibody to Treat Waldenstrom's Macroglobulinemia

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

The purpose of this study is to determine the safety and effects (good or bad) of Campath-1H antibody in the treatment of lymphoplasmacytic lymphoma.

NCT ID: NCT00142129 Completed - Clinical trials for Lymphoplasmacytic Lymphoma

Bortezomib (Velcade) in Waldenstrom's Macroglobulinemia

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

The purpose of this study is to evaluate how tumors in patients with Waldenstrom's macroglobulinemia respond to treatment with bortezomib (Velcade) and to see what effects (good and bad) it has on the cancer.

NCT ID: NCT00142116 Completed - Clinical trials for Lymphoplasmacytic Lymphoma

Thalidomide and Rituximab in Waldenstrom's Macroglobulinemia

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

The purpose of this study is to determine the percentage of people who can attain remission and the length of time such responses to therapy are sustained, as well as the side effects that might result from rituximab and thalidomide in people with lymphoplasmacytic lymphoma.