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Myelodysplastic Syndromes 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: NCT01908387 Terminated - Multiple Myeloma Clinical Trials

Phase 1 Study of CC-486 in Japanese Subjects With Hematological Neoplasms

Start date: July 2013
Phase: Phase 1
Study type: Interventional

To identify the maximum tolerated dose (MTD) of oral azacitidine on different treatment schedules in Japanese subjects with hematological neoplasms

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: NCT01902381 Terminated - Clinical trials for Previously Treated Myelodysplastic Syndromes

CPI-613 in Treating Patients With Myelodysplastic Syndromes Who Failed Previous Therapy

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

This pilot clinical trial studies 6, 8-bis (benzylthio) octanoic acid (CPI-613) in treating patients with myelodysplastic syndromes who failed previous therapy. Sometimes when chemotherapy or biological therapy is given, it does not stop the growth of tumor cells. The tumor is said to be resistant to treatment. 6, 8-bis (benzylthio) octanoic acid may interfere with the growth of tumor cells and may be an effective treatment for myelodysplastic syndromes that did not respond to previous therapy.

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: NCT01894477 Active, not recruiting - Clinical trials for Myelodysplastic Syndrome

Treo/Flu/TBI With Donor Stem Cell Transplant for Patients With Myelodysplastic Syndrome or Acute Myeloid Leukemia

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

This randomized phase II trial studies how well treosulfan and fludarabine phosphate, with or without total body irradiation before donor stem cell transplant works in treating patients with myelodysplastic syndrome or acute myeloid leukemia. Giving chemotherapy, such as treosulfan and fludarabine phosphate, and total-body irradiation before a donor stem cell transplant helps stop the growth of cancer cells. It may also stop the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune cells and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving tacrolimus before and mycophenolate mofetil after the transplant may stop this from happening.

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.