Clinical Trials Logo

Myelodysplastic Syndromes clinical trials

View clinical trials related to Myelodysplastic Syndromes.

Filter by:

NCT ID: NCT02029950 Completed - Clinical trials for Acute Myeloid Leukemia

Pomalidomide After Combination Chemotherapy in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndrome

Start date: December 16, 2013
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of pomalidomide after combination chemotherapy in treating patients with newly diagnosed acute myeloid leukemia or high-risk myelodysplastic syndrome. Drugs used in chemotherapy, such as cytarabine, daunorubicin hydrochloride, and etoposide, 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. Pomalidomide may kill cancer cells by stopping blood flow to the cancer and by stimulating white blood cells to kill cancer cells. Giving more than one drug (combination chemotherapy) and pomalidomide may kill more cancer cells.

NCT ID: NCT02029417 Terminated - Clinical trials for Adult Acute Myeloid Leukemia With 11q23 (MLL) Abnormalities

Omacetaxine Mepesuccinate, Cytarabine, and Decitabine in Treating Older Patients With Newly Diagnosed Acute Myeloid Leukemia

Start date: July 2014
Phase: Phase 2
Study type: Interventional

This phase II trial studies the side effects and how well omacetaxine mepesuccinate, cytarabine, and decitabine work in treating older patients with newly diagnosed acute myeloid leukemia. Omacetaxine mepesuccinate, cytarabine, and decitabine may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.

NCT ID: NCT02019069 Completed - Clinical trials for Recurrent Adult Acute Myeloid Leukemia

CPX-351 in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome

Start date: February 3, 2014
Phase: Phase 2
Study type: Interventional

This phase 2 clinical trial studies how well CPX-351 (liposomal cytarabine-daunorubicin) works in treating patients with relapsed or refractory acute myeloid leukemia or myelodysplastic syndrome. Drugs used in chemotherapy, such as CPX-351, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing.

NCT ID: NCT02018926 Completed - Clinical trials for Myelodysplastic Syndrome

Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS

Start date: December 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Mocetinostat is an orally administered histone deacetylase (HDAC) inhibitor. Azacitidine is a hypomethylating agent (HMA) used to treat MDS. In this study, patients with intermediate- or high-risk MDS will receive treatment with mocetinostat and azacitidine to evaluate the safety of the study treatment. Safety assessments will include echocardiograms, electrocardiograms and routine safety laboratory studies (hematology and serum chemistry). In addition, clinical response to treatment will be monitored using bone marrow aspirates or biopsies, and other routine methods.

NCT ID: NCT02017457 Completed - Clinical trials for Myelodysplastic Syndrome

Azacytidine and Lymphocytes in Relapse of AML or MDS After Allogeneic Stem Cell Transplantation.

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

The present project is a multicenter, phase II trial which aims at evaluating if the administration of azacytidine (Vidaza®) combined to donor lymphocyte infusion (DLI) could improve the response rate to DLI in the population of patients with relapsed acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) after allogeneic hematopoietic stem cell transplantation.

NCT ID: NCT02016781 Completed - MDS Clinical Trials

Allo vs Hypomethylating/Best Supportive Care in MDS (BMTCTN1102)

Start date: December 16, 2013
Phase: Phase 2
Study type: Interventional

This study is designed as a multicenter trial, with biological assignment to one of two study arms; Arm 1: Reduced intensity conditioning allogeneic hematopoietic cell transplantation (RIC-alloHCT), Arm 2: Non-Transplant Therapy/Best Supportive Care.

NCT ID: NCT02014051 Completed - Clinical trials for Myelodysplastic Syndrome

Safety and Pharmacokinetics Study of SyB C-1101 in Patients With Recurrent/Relapsed or Refractory Myelodysplastic Syndrome (MDS)

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

The purpose of this study is to investigate tolerability when SyB C-1101 is orally administered twice daily for 14 consecutive days to the patients with recurrent/relapsed or refractory myelodysplastic syndrome, to determine the dose-limiting toxicity and maximum tolerated dose, and to estimate the recommended dose for phase II studies. Pharmacokinetics and antitumor effects will also be investigated.

NCT ID: NCT02013102 Recruiting - Clinical trials for Myelodysplastic Syndrome

A Phase Ⅳ Study of Decitabine in Myelodysplastic Syndrome

DREAM
Start date: March 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate of the safety and efficacy of decitabine treatment of Myelodysplastic Syndrome.

NCT ID: NCT02010645 Terminated - Leukemia Clinical Trials

Eltrombopag With Decitabine in Advanced Myelodysplastic Syndrome (MDS)

Start date: March 2014
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if eltrombopag given in combination with decitabine can help to control advanced MDS. The safety of this study drug combination will also be studied.

NCT ID: NCT02008318 Completed - Clinical trials for Myelodysplastic Syndromes

A Study of Galunisertib in Participants With Myelodysplastic Syndromes

Start date: March 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to investigate the effect of the study drug known as galunisertib in participants with myelodysplastic syndromes (MDS). Participants with different degrees of disease (very low, low, and intermediate risk) will be studied. The study treatment is expected to last about 6 months for each participant.