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Leukemia, Myeloid clinical trials

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NCT ID: NCT00428558 Completed - Clinical trials for Acute Myeloid Leukemia

Timed-Sequential Induction in CBF-AML

Start date: July 2007
Phase: Phase 3
Study type: Interventional

Core binding factor (CBF) acute myeloid leukemias (AML) include AMLs carrying the t(8;21) translocation as well as AMLs carrying either the inversion of chromosome 16 or translocation t(16;16). CBF-AMLs are characterized by their high sensitivity to standard chemotherapeutical agents, especially to cytarabine when administered as high-dose bolus infusions, and thus by a relative good prognosis. However, relapse rates are still comprised between 30 and 50% in these patients, even if overall survival may reach approximately 65% due to the potential salvage of late relapses. The primary purpose of the protocol is to compare two modalities of timed-sequential induction in order to improve the results of the treatment of CBF-AML patients. This protocol also includes the biological characterization of the heterogeneity of these diseases (gene mutation and transcription profiles), as well as a centralized minimal residual disease monitoring and centralized evaluation of pharmacogenetic polymorphisms.

NCT ID: NCT00428077 Terminated - Leukemia Clinical Trials

Vaccine Therapy in Treating Patients With Chronic Phase Chronic Myelogenous Leukemia

Start date: October 2005
Phase: Phase 2
Study type: Interventional

RATIONALE: Vaccines made from a peptide may help the body build an effective immune response to kill cancer cells. PURPOSE: This phase II trial is studying how well vaccine therapy works in treating patients with chronic phase chronic myelogenous leukemia.

NCT ID: NCT00426205 Completed - Clinical trials for Refractory Acute Myeloid Leukemia

GM-CSF Vaccinations After Allogeneic Blood Stem Cell Transplantation in Patients With Advanced Myeloid Malignancies

Start date: June 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether the addition of a vaccine after participants reduced intensity transplant will be safe and beneficial. The vaccine used in this trial, called GVAX, will be made from the participants own leukemia cells, and will be given between 1-4 months after transplant. In recent years, researchers have discovered that GVAX vaccine made from the patient's own cancer calls that have been engineered in the laboratory to produce a protein called GM-CSF, can be effective in stimulating a powerful immune response specific to that cancer.

NCT ID: NCT00425477 Completed - Leukemia Clinical Trials

Bexarotene and GM-CSF in Treating Patients With Myelodysplastic Syndrome or Acute Myeloid Leukemia

Start date: November 2006
Phase: Phase 2
Study type: Interventional

RATIONALE: Bexarotene may help cancer or abnormal cells become more like normal cells, and to grow and spread more slowly. Colony-stimulating factors, such as GM-CSF, may increase the number of immune cells found in bone marrow or peripheral blood. Giving bexarotene together with GM-CSF may be an effective treatment for myelodysplastic syndrome (MDS) or acute myeloid leukemia. PURPOSE: This phase II trial is studying how well giving bexarotene together with GM-CSF works in treating patients with MDS or acute myeloid leukemia.

NCT ID: NCT00422890 Completed - Clinical trials for Myelodysplastic Syndrome

Treatment of Imminent Haematological Relapse in Patients With AML and MDS Following Allogeneic Stem Cell Transplantation With 5-azacitidine (Vidaza®)

Start date: January 2007
Phase: Phase 3
Study type: Interventional

Efficacy and safety of 5-Azacytidin in the treatment of the haematological relapse in patients suffering from acute myeloid leukaemia or myelodysplastic syndrome with falling CD34-chimerism after hematopoietic stem cell transplantation.

NCT ID: NCT00422591 Completed - Leukemia Clinical Trials

Standard Idarubicin and Cytarabine for the Treatment of Acute Myeloid Leukemia (AML)

Start date: December 2006
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to find out if standard chemotherapy given with idarubicin and Cytarabine (ara-C) can help to control AML. Objectives: To determine the complete response (CR) rate, event-free survival (EFS) and overall survival (OS) of patients with newly diagnosed acute myeloid leukemia (AML) receiving standard combination chemotherapy with Idarubicin and cytarabine.

NCT ID: NCT00418951 Completed - Clinical trials for Myelodysplastic Syndrome

Liposomal Amphotericin B (Ambisome) Versus Oral Voriconazole for the Prevention of Invasive Fungal Infections

Start date: November 2006
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to compare the effectiveness of liposomal amphotericin B given three times per week , versus liposomal amphotericin B given once per week, versus oral voriconazole in the prevention of fungal infections in patients with acute myeloid leukemia (AML) or myelodysplastic syndromes MDS who are receiving chemotherapy. The safety of these treatments will also be studied and compared.

NCT ID: NCT00416598 Completed - Clinical trials for Acute Myeloid Leukemia

Decitabine as Maintenance Therapy After Standard Therapy in Treating Patients With Previously Untreated Acute Myeloid Leukemia

Start date: November 15, 2006
Phase: Phase 2
Study type: Interventional

This phase II trial is studying the side effects and how well decitabine works when given as maintenance therapy after standard therapy in treating patients with previously untreated acute myeloid leukemia. Drugs used in chemotherapy, such as cytarabine, daunorubicin, etoposide, busulfan, and decitabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving decitabine as maintenance therapy after standard therapy may keep cancer cells from coming back.

NCT ID: NCT00415909 Terminated - Clinical trials for Chronic Myelogenous Leukemia

TALL-104 and Gleevec in Chronic Myelogenous Leukemia Patients

Start date: December 2006
Phase: Phase 2
Study type: Interventional

Objectives: - To determine the response rate and duration of response with combination of TALL-104 cells and imatinib mesylate (IM) therapy in patients with chronic myelogenous leukemia in chronic phase, that have not achieved, or have lost, adequate response to IM. - To determine the toxicity of the combination of TALL-104 cells and IM therapy in this patient population.

NCT ID: NCT00414310 Completed - Clinical trials for Myelodysplastic Syndrome

Decitabine (DAC) w/ or w/o Valproic Acid (VPA) in Myelodysplastic Syndrome (MDS) and Acute Myelogenous Leukemia (AML)

Start date: December 2006
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to find out if decitabine, given with or without valproic acid, can help to control AML or MDS. The safety of both treatments will also be studied.