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Preleukemia clinical trials

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NCT ID: NCT01913951 Completed - Clinical trials for Myelodysplastic Syndromes

Vosaroxin and Azacitidine in Treating Patients With Myelodysplastic Syndromes

Start date: November 22, 2013
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and the best dose of vosaroxin when given together with azacitidine in treating patients with myelodysplastic syndromes. Drugs used in chemotherapy, such as vosaroxin and azacitidine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing.

NCT ID: NCT01911871 Completed - Sickle Cell Disease Clinical Trials

Multicenter Observational Study on Myocardial Iron Overload in 3 Multitransfused Populations

SUFEMYO
Start date: March 2012
Phase: N/A
Study type: Observational

The investigators' primary objective is to study prevalences of myocardial iron overload, defined as a cardiac T2*< 20 ms, in 3 populations of multiply transfused patients, affected with thalassemia, sickle cell disease, and myelodysplasia.

NCT ID: NCT01904682 Completed - Clinical trials for Myelodysplastic Syndromes

Oral Rigosertib in Low Risk MDS Patients Refractory to ESAs

Start date: July 2013
Phase: Phase 2
Study type: Interventional

The study will enroll low risk MDS patients who need red blood cell transfusions and who are refractory to or are not using erythropoiesis-stimulating agents. The purpose of the study is to determine whether oral rigosertib treatment results in hematological improvements according to the 2006 International Working Group criteria in these patients. The study will also record any side effects that may occur during the study.

NCT ID: NCT01904175 Completed - Leukemia Clinical Trials

Registry Study of T Cell Depleted Allo Non-Myeloablative Stem Cell Transplant

Start date: August 2013
Phase: N/A
Study type: Observational [Patient Registry]

Allogeneic transplantation is used to treat many malignant and non-malignant diseases. The investigators and others have shown that less toxic preparative regimens (reduced intensity or 'mini' transplants) allow reliable allogeneic engraftment and durable remissions, significantly broadening the population of patients who may be offered this therapy to those who are older and more infirmed. The field is now focusing on the period post transplant for approaches to immune recovery leading to improved outcomes. The primary objective of this registry is to catalogue data from patients who undergo standard of care reduced intensity allogeneic transplantation.

NCT ID: NCT01904136 Completed - Clinical trials for Myelodysplastic Syndrome

Natural Killer Cells Before and After Donor Stem Cell Transplant in Treating Patients With Acute Myeloid Leukemia, Myelodysplastic Syndrome, or Chronic Myelogenous Leukemia

Start date: April 22, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II studies the side effects and best dose of natural killer cells before and after donor stem cell transplant and to see how well they work in treating patients with acute myeloid leukemia, myelodysplastic syndrome, or chronic myelogenous leukemia. Giving chemotherapy with or without total body irradiation before a donor peripheral blood stem cell or bone marrow transplant helps stop the growth of cancer cells. It may also stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells and natural killer cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets.

NCT ID: NCT01895842 Completed - Leukemia Clinical Trials

Ruxolitinib for Patients With Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS)

Start date: February 2014
Phase: Phase 1
Study type: Interventional

The goal of this clinical research study is to find the highest tolerable dose of ruxolitinib that can be given to patients with low or intermediate-1 risk MDS. The safety of this drug will also be studied, and whether it can help to control the disease.

NCT ID: NCT01893372 Completed - Leukemia Clinical Trials

Eltrombopag With or Without Hypomethylating Agent After Hypomethylating Agent Failure For Patients With Myelodysplastic Syndrome (MDS)

Start date: October 2013
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if eltrombopag can help to control MDS. The safety of this drug will also be studied.

NCT ID: NCT01893320 Completed - Leukemia Clinical Trials

Study of Vosaroxin and Decitabine in Older Patients With Acute Myeloid Leukemia and High-risk Myelodysplastic Syndrome

Start date: July 18, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if the combination of vosaroxin and decitabine can help to control AML or MDS. The safety of these drugs will also be studied.

NCT ID: NCT01892371 Completed - Clinical trials for Refractory Acute Myeloid Leukemia

Quizartinib With Azacitidine or Cytarabine in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome

Start date: November 12, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II trial studies the side effects and best dose of quizartinib when given in combination with azacitidine or cytarabine in treating patients with acute myeloid leukemia or myelodysplastic syndrome that have come back (relapsed) or are not responding to treatment (refractory). Quizartinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as azacitidine and cytarabine work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving quizartinib with azacitidine or cytarabine may work better in patients with acute myeloid leukemia or myelodysplastic syndrome.

NCT ID: NCT01891968 Completed - Leukemia Clinical Trials

Bortezomib for Low or Intermediate-1 Myelodysplastic Syndrome (MDS) With p65 Activation

Start date: August 7, 2013
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if bortezomib can help to control MDS. The safety of this drug will also be studied. Bortezomib is designed to block a protein that causes cells to grow. This may cause cancer cells to die.