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Lymphoma clinical trials

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NCT ID: NCT00038883 Terminated - Lymphoma, B-Cell Clinical Trials

Campath-1H and Allogeneic Blood Stem Cell Transplantation for Lymphoid Malignancies

Start date: April 9, 2001
Phase: N/A
Study type: Interventional

High dose chemotherapy followed by transplantation of allogeneic hematopoietic stem cell with the use of Campath-1h, a monoclonal antibody that have a synergistic effect to chemotherapy with minimal toxicity. In addition Campath-1H can improve engraftment of donor cells through its immunosuppressive properties.

NCT ID: NCT00038857 Completed - Lymphoma Clinical Trials

Megadose CD34 Selected Progenitor Cells for Transplantation in Patients With Advanced Hematological Malignant Diseases

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

Donor: This clinical study will evaluate the feasibility of a purified CD34 peripheral blood progenitor cell (PBPC) transplants in patients with hematological malignancies. The primary objectives of the study are to evaluate the recipient obtaining donor derived neutrophil engraftment and the incidence of acute graft versus host disease [GvHD] (grade III-IV). Secondary objectives include assessments of recipient having donor derived platelet engraftment, incidence of graft failure and chronic GvHD, overall and disease free survival, clinical safety and device performance of the CliniMACS CD34 selection device.

NCT ID: NCT00038844 Completed - Lymphoma Clinical Trials

Safety and Efficacy of Campath in Nonmyeloablative Transplantation

Start date: June 2001
Phase: N/A
Study type: Interventional

Objective of the low-dose transplant regimen must produce the following effects: 1. Suppression of the patient's immune system to prevent rejection of the donor cells; 2. Control of the lymphoma. The pretransplant regimen must suppress the lymphoma sufficiently to prevent marked progression of the tumor and allow time for the GVT effect to occur.

NCT ID: NCT00038623 Completed - Clinical trials for Lymphoma, Mantle-Cell

Study Of Yttrium-ibritumomab (Zevalin) For the Treatment Of Patients With Relapsed And Refractory Mantle Cell Lymphoma

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

Study of Yttrium-ibritumomab (Zevalin) For the treatment of Patients with Relapsed & Refractory Mantle Cell Lymphoma

NCT ID: NCT00038571 Completed - Lymphoma, B-Cell Clinical Trials

Proteasome Inhibitor PS-341 Relapsed or Refractory B Cell Lymphomas Previously Treated With Chemotherapy

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

Purpose of Phase II study for B-cell lymphoma using PS341: Evaluate efficacy and toxicity of bortezomib in patients with relapsed or refractory B-cell non-Hodgkin's lymphoma.

NCT ID: NCT00038545 Completed - Clinical trials for Non-Hodgkin's Lymphoma

A Phase II Study of Paclitaxel and Topotecan With Filgrastim-SD/01 Support For Relapsed and Refractory Aggressive Non-Hodgkin's Lymphoma

Start date: May 18, 2001
Phase: Phase 2
Study type: Interventional

For patients with relapsed and refractory aggressive non-Hodgkin's lymphoma

NCT ID: NCT00038207 Completed - Lymphoma Clinical Trials

Liposomal Vincristine for Pediatric and Adolescent Patients With Relapsed Malignancies

Start date: June 2000
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if treatment with the drug liposomal vincristine can shrink or slow the growth of the patient's cancer. The safety of this drug will also be studied.

NCT ID: NCT00038025 Completed - Clinical trials for Chronic Lymphocytic Leukemia

A Study Of Deoxycoformycin(DCF)/Pentostatin In Lymphoid Malignancies

Start date: September 6, 1994
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the side effects and antitumor response of patients with lymphoid malignancies to Deoxycoformycin (DCF)/Pentostatin.

NCT ID: NCT00037791 Completed - Multiple Myeloma Clinical Trials

Safety and Efficacy of (PN-152,243)/PN-196,444 in the Prevention of Thrombocytopenia

Start date: December 1999
Phase: Phase 3
Study type: Interventional

Intensive chemotherapy is associated with significant thrombocytopenia, often requiring platelet transfusion to maintain platelet counts. This investigational drug has demonstrated the ability to increase platelet counts. This study will test the safety and efficacy of this investigational drug in the prevention of thrombocytopenia in patients with solid tumors, lymphomas or multiple myeloma who are receiving myelosuppressive treatment regimens requiring platelet transfusion support.

NCT ID: NCT00036946 Completed - Lymphoma Clinical Trials

VEGF Trap in Treating Patients With Relapsed or Refractory Solid Tumors or Non-Hodgkin's Lymphoma

Start date: November 2001
Phase: Phase 1
Study type: Interventional

RATIONALE: VEGF Trap may stop the growth of solid tumors or non-Hodgkin's lymphoma by stopping blood flow to the cancer. PURPOSE: Phase I trial to study the effectiveness of VEGF Trap in patients who have relapsed or refractory solid tumors or non-Hodgkin's lymphoma.