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Leukemia clinical trials

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NCT ID: NCT01472107 Completed - Pregnancy Clinical Trials

Study on Number and Outcome of Pregnancy in Acute Promielocitic Leukaemia (APL) Patients Treated With Chemotherapy

APL0511
Start date: March 7, 2012
Phase:
Study type: Observational

The GIMEMA FOUNDATION promotes an observational (retrospective) study on number and outcome of pregnancy in childbearing age female patients treated with chemotherapy for APL. These patients were enrolled in studies AIDA0493, AIDA2000 and were in CR.

NCT ID: NCT01472055 Recruiting - Acute Leukemia Clinical Trials

Pharmacokinetic Study of Fludarabine in Pediatric Hematopoietic Stem Cell Transplantation

Start date: October 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to analysis of the pharmacokinetics of fludarabine for hematopoietic stem cell transplantation in pediatric patients.

NCT ID: NCT01471782 Completed - Clinical trials for Acute Lymphoblastic Leukemia

Clinical Study With Blinatumomab in Pediatric and Adolescent Patients With Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the dose of the bispecific T cell engager blinatumomab (MT103) in pediatric and adolescent patients with relapsed/refractory Acute Lymphoblastic Leukemia (ALL) and to assess whether this dose of blinatumomab is effective.

NCT ID: NCT01471444 Completed - Leukemia Clinical Trials

Fludarabine-IV Busulfan ± Clofarabine and Allogeneic Hematopoietic Stem Cell Transplantation for Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS)

Start date: November 2, 2011
Phase: Phase 3
Study type: Interventional

The goal of this clinical research study is to learn if combining busulfan with clofarabine and fludarabine can help control the disease better than the previous standard method (using busulfan and fludarabine alone) in patients with AML or MDS. The safety of this combination therapy will also be studied.

NCT ID: NCT01471067 Completed - Lymphoma Clinical Trials

Cord Blood Fucosylation to Enhance Homing and Engraftment in Patients With Hematologic Malignancies

Start date: July 13, 2012
Phase: Phase 1
Study type: Interventional

The goal of this clinical research study is to learn if it is safe and feasible to transplant changed cord blood for patients with leukemia or lymphoma. Researchers also want to learn if this can help to control the disease. The cord blood will be changed to make use of sugar that is found in small amounts in blood cells. It plays a role in signaling where in the body the transplanted cells should go to. Adding more sugars to the cord blood cells in the laboratory is designed to help the cord blood cells find their way faster to the bone marrow. This may help your blood counts to recover faster. This process is called fucosylation. Anti-thymocyte globulin (ATG) is a protein that removes immune cells that cause damage to the body. Clofarabine is designed to interfere with the growth and development of cancer cells. Fludarabine is designed to interfere with the DNA (genetic material) of cancer cells, which may cause the cancer cells to die. This chemotherapy is also designed to block your body's ability to reject the donor's bone marrow cells. Melphalan and busulfan are designed to bind to the DNA of cells, which may cause cancer cells to die. Mycophenolate mofetil (MMF) and tacrolimus are designed to block the donor cells from growing and spreading in a way that could cause graft versus host disease (GVHD -- a condition in which transplanted tissue attacks the recipient's body). This may help to prevent GVHD. Rituximab is designed to attach to cancer cells, which may cause them to die.

NCT ID: NCT01470924 Completed - Clinical trials for Acute Lymphoblastic Leukemia

Acute Lymphoblastic Leukemia Relapse in Sweden 2003-2007

Start date: January 2003
Phase: N/A
Study type: Observational

A minority of patients with adult acute lymphoblastic leukemia (ALL) relapse are rescued. The aim of this population-based study was to assess the results of reinduction treatment and allogeneic stem cell transplantation (SCT) in second complete remission (CR) in Sweden 2003-2007.

NCT ID: NCT01468467 Completed - Clinical trials for Leukemia, Myeloid, Acute

A Study of AC220 Given After Transplant in Subjects With Acute Myeloid Leukemia (AML)

Start date: April 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to define a safe dose of AC220 when given as maintenance therapy after treatment with an allogeneic stem cell transplant.

NCT ID: NCT01466179 Active, not recruiting - Clinical trials for Acute Lymphoblastic Leukemia

Clinical Study With Blinatumomab in Patients With Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia (ALL)

Start date: December 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to confirm whether the bispecific T cell engager antibody blinatumomab (MT103) is effective and safe in the treatment of patients with relapsed or refractory Acute Lymphoblastic Leukemia (ALL).

NCT ID: NCT01465386 Terminated - Clinical trials for Adult Acute Myeloid Leukemia With 11q23 (MLL) Abnormalities

Bortezomib in Treating Patients With High-Risk Acute Myeloid Leukemia in Remission

Start date: November 2011
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well bortezomib works in treating patients with high-risk acute myeloid leukemia (AML) in remission. Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth

NCT ID: NCT01465230 Terminated - Clinical trials for Chronic Lymphocytic Leukemia

Maintenance Therapy: Lenalidomide Following Bendamustine and Rituximab Induction Therapy for Chronic Lymphocytic Leukemia

Start date: March 2012
Phase: Phase 2
Study type: Interventional

This study will determine whether or not Lenalidomide improves effectiveness of treatment for chronic lymphocytic leukemia following chemotherapy with two drugs commonly used to treat the disease (bendamustine and rituximab).