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Lymphoma clinical trials

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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.

NCT ID: NCT00036790 Completed - Breast Cancer Clinical Trials

Motexafin Gadolinium and Doxorubicin in Treating Patients With Advanced Cancer

Start date: February 2002
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Motexafin gadolinium may increase the effectiveness of doxorubicin by making tumor cells more sensitive to the drug. PURPOSE: Phase I trial to study the effectiveness of combining motexafin gadolinium with doxorubicin in treating patients who have recurrent or metastatic cancer.

NCT ID: NCT00036023 Completed - Multiple Myeloma Clinical Trials

Chemotherapy Related Anemia in Patients With Non-Myeloid Malignancies

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

Chemotherapy can often cause anemia in patients with cancer. Anemia is a low number of red blood cells. The symptoms of anemia may include fatigue, dizziness, headache, chest pain, and shortness of breath. Erythropoietin is a hormone made by the kidneys that signals the bone marrow to produce more red blood cells. Recombinant human erythropoietin has been produced in the laboratory and has the same effect as the hormone produced by the body. Use of recombinant human erythropoietin allows the body to produce more red blood cells, possibly eliminating or decreasing your symptoms and the need for a red blood cell transfusion. Recombinant human erythropoietin is FDA approved to treat anemia in cancer patients receiving chemotherapy. This clinical study is investigating the effectiveness of darbepoetin alfa for the treatment of anemia in patients with non-myeloid malignancies who are receiving chemotherapy every three weeks. Darbepoetin alfa is a recombinant erythropoietic protein that stimulates the production of red blood cells. This medication has not been approved to treat cancer patients with anemia, however it has been approved by the FDA to treat chronic renal failure patients with anemia.

NCT ID: NCT00035022 Completed - Lymphoma Clinical Trials

Study of Intravenous BCX-1777 in Relapsed or Refractory Aggressive T-Cell Leukemias or Lymphomas

Start date: August 2001
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if intravenous BCX-1777 can be given safely to improve relapsed or refractory aggressive T-cell leukemias and lymphomas.

NCT ID: NCT00033267 Completed - Clinical trials for Recurrent Mantle Cell Lymphoma

CCI-779 in Treating Patients With Mantle Cell Non-Hodgkin's Lymphoma

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

Phase II trial to study the effectiveness of CCI-779 in treating patients who have mantle cell non-Hodgkin's lymphoma. Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die.

NCT ID: NCT00032019 Completed - Lymphoma Clinical Trials

Combination Chemotherapy and Monoclonal Antibody Therapy in Treating Patients With Non-Hodgkin's Lymphoma

Start date: February 2002
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. Monoclonal antibodies such as rituximab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Combining rituximab with combination chemotherapy may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of combining rituximab with combination chemotherapy in treating patients who have previously untreated non-Hodgkin's lymphoma.

NCT ID: NCT00031941 Completed - Lymphoma Clinical Trials

CC-5013 in Treating Patients With Cancer That Has Not Responded to Previous Therapy

Start date: April 2002
Phase: Phase 1
Study type: Interventional

RATIONALE: CC-5013 may stop the growth of cancer by stopping blood flow to the tumor. PURPOSE: Phase I trial to study the effectiveness of CC-5013 in treating patients who have solid tumors and/or lymphoma that did not respond to previous therapy.