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Leukemia, Lymphoid clinical trials

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NCT ID: NCT00658411 Terminated - Clinical trials for Acute Myeloid Leukemia

Deferoxamine for Iron Overload Before Allogeneic Stem Cell Transplantation

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

The objective of this research study is to determine the safety and feasibility of chelation therapy with deferoxamine for patients with iron overload who are receiving a stem cell transplant. Patients who have iron overload prior to stem cell transplantation may have more toxicity from the transplantation procedure, and thus may benefit from an attempt at iron chelation pre- and peri-transplantation. In this study we are examining the use of deferoxamine starting 2 weeks to 3 months prior to transplantation and continuing through the preparative regimen.

NCT ID: NCT00648739 Terminated - Multiple Myeloma Clinical Trials

Safety and Dose Ranging Study of Samalizumab to Treat Relapsing or Refractory CLL or MM

Start date: June 19, 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study was to determine the safety and maximum tolerated dose (MTD) of ALXN6000 (samalizumab) in treating relapsing or refractory B-cell chronic lymphocytic leukemia (B-CLL) or multiple myeloma (MM) and to study how samalizumab may help the immune system fight tumors that express CD200.

NCT ID: NCT00646165 Terminated - Clinical trials for B-cell Chronic Lymphocytic Leukemia

Trial of Forodesine in Patients With Relapsed B-cell Chronic Lymphocytic Leukemia

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

To determine the dose and duration of treatment for the best overall response with Forodesine in relapsed B-cell chronic lymphocytic leukemia

NCT ID: NCT00643240 Terminated - Leukemia Clinical Trials

Yttrium Y 90 Anti-CD19 Antibody BU-12 in Patients With Advanced Relapsed or Refractory Acute Lymphoblastic Leukemia or Chronic Lymphocytic Leukemia

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

RATIONALE: Radiolabeled monoclonal antibodies can find cancer cells and carry cancer-killing substances to them without harming normal cells. This may be effective treatment for leukemia. PURPOSE: This phase I trial is studying the best dose of yttrium Y 90-labeled monoclonal antibody BU-12 in treating patients with advanced relapsed or refractory acute lymphoblastic leukemia or chronic lymphocytic leukemia.

NCT ID: NCT00636155 Terminated - Clinical trials for Leukemia, Lymphocytic, Chronic

EL625 in Persistent Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

Start date: February 2008
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to see if the investigational drug EL625, when combined with traditional chemotherapy (rituximab, fludarabine, and cyclophosphamide), is effective in Persistent Chronic Lymphocytic Leukemia (CLL) and Small Lymphocytic Lymphoma (SLL)

NCT ID: NCT00625729 Terminated - Lymphoma Clinical Trials

Donor Natural Killer Cell Infusion, Rituximab, Aldesleukin, and Chemotherapy in Treating Patients With Relapsed Non-Hodgkin Lymphoma or Chronic Lymphocytic Leukemia

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

RATIONALE: Aldesleukin may stimulate natural killer cells to kill cancer cells. Treating natural killer cells with aldesleukin in the laboratory may help the natural killer cells kill more cancer cells when they are put back in the body. Giving monoclonal antibodies, such as rituximab, and chemotherapy drugs, such as fludarabine and cyclophosphamide, before a donor natural killer cell infusion helps stop the growth of cancer cells. It also helps stop the patient's immune system from rejecting the donor's stem cells. PURPOSE: This phase I/II trial is studying how well giving rituximab and chemotherapy followed by a donor natural killer cell infusion that has been treated in the laboratory with aldesleukin followed by aldesleukin works in treating patients with non-Hodgkin lymphoma or chronic lymphocytic leukemia.

NCT ID: NCT00612612 Terminated - Leukemia Clinical Trials

Obatoclax, Fludarabine, and Rituximab in Treating Patients With Previously Treated Chronic Lymphocytic Leukemia

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

Obatoclax may stop the growth of chronic lymphocytic leukemia by blocking blood flow to the cancer and by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as fludarabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. 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. Giving obatoclax together with fludarabine and rituximab may kill more cancer cells. This phase I trial is studying the side effects and best dose of obatoclax when given together with fludarabine and rituximab in treating patients with B-cell chronic lymphocytic leukemia.

NCT ID: NCT00596336 Terminated - Clinical trials for Chronic Lymphocytic Leukemia

Study of Immune Responses to Influenza Vaccination With or Without Imiquimod Application in Untreated CLL Patients

CLLIFVAC
Start date: October 2007
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine whether it is possible to improve the immune response rate to 'flu vaccination in patients with chronic lymphocytic leukaemia (CLL). Annual flu vaccination is recommended for all patients with CLL because they are known to be susceptible to infections and particularly to chest infections that may occur as a complication of influenza. Protection against 'flu depends on patients having a high level of antibodies against the 'flu virus. Vaccination works by stimulating the immune system and thus boosting the levels of these protective antibodies. CLL patients have weakened immune systems due to the leukaemia itself but also following chemotherapy. The exact cause of these immune defects is not known. However, CLL patients typically have low antibody levels and their immune cells may not work normally. Unfortunately, studies have shown that patients with CLL are not very good at making antibodies to 'flu vaccination and as a result protection against flu is not very reliable. Recent studies have shown that only 15-20 % of CLL patients will achieve a protective antibody level. Recently a new type of medical cream has been introduced to treat certain skin conditions. Its name is Imiquimod and it is licensed to treat viral warts in the genital area and a type of skin cancer called basal cell carcinoma. It works by increasing the immune response in the skin. Animal studies have shown that as well as increasing immunity against viruses and cancers, it increases responses to vaccination when applied at the site of vaccination. In this study we propose to test whether this new medicine can improve the response to the 'flu jab.

NCT ID: NCT00594308 Terminated - Multiple Myeloma Clinical Trials

In-Vivo Activated T-Cell Depletion to Prevent GVHD

Start date: October 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects (good and bad) of the medication basiliximab in combination with cyclosporine with cyclosporine alone for the prevention of graft-versus-host disease. This research is being done because there is no completely safe and effective prevention for graft-versus-host disease. It is known that cyclosporine helps with GVHD but we would like to know if the addition of basiliximab will decrease the incidence and/or severity of GVHD after a transplant known as nonmyeloablative ("mini" transplant).

NCT ID: NCT00593554 Terminated - Clinical trials for Acute Myeloid Leukemia

Phase 2 Haplotype Mismatched HSCT in Patients With Hematological Malignancies

Start date: August 7, 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if haplotype-mismatched HSCT is associated with an improvement in treatment-related mortality (TRM) rate at 6 months.