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Myelodysplastic Syndrome (MDS) clinical trials

View clinical trials related to Myelodysplastic Syndrome (MDS).

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NCT ID: NCT02147873 Terminated - Clinical trials for Myelodysplastic Syndrome (MDS)

Study of Azacitidine With or Without Birinapant in Subjects With MDS or CMMoL

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

This is a randomized double blind placebo controlled study of azacitidine with or without birinapant in subjects with higher risk Myelodysplastic syndrome, secondary MDS or myelomonocytic leukemia (CMMoL) who are naïve, to azacitidine therapy. Pre-clinical and mechanistic studies support that azacitidine may modulate pathways that enable birinapant-mediated anti-tumor activity.

NCT ID: NCT01459159 Terminated - Clinical trials for Myelodysplastic Syndrome (MDS)

Study of (Telintra®) in Non-Del(5q) Myelodysplastic Syndrome

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

This is a multicenter, single arm open label Phase 2b Study of oral ezatiostat (Telintra®) in Patients who are RBC tranfusion dependent, Low to INT-1 IPSS risk, non-del (5q) Myelodysplastic Syndrome (MDS).

NCT ID: NCT01422486 Terminated - Clinical trials for Myelodysplastic Syndrome (MDS)

Phase 2 Study of Telintra® in Deletion 5q Myelodysplastic Syndrome

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

Study TLK199.2107 is a multicenter, single arm, open-label Phase 2 study of oral ezatiostat (Telintra®) in patients with lenalidomide (Revlimid®) refractory or resistant, red blood cell (RBC) transfusion-dependent, Low to Intermediate-1 IPSS risk, del5q Myelodysplastic Syndrome (MDS).

NCT ID: NCT01362036 Terminated - Clinical trials for Myelodysplastic Syndrome (MDS)

Phase I Study Evaluating TXA127 in Low/Intermediate-1 Risk Myelodysplastic Syndrome and Thrombocytopenia

Start date: April 2011
Phase: Phase 1
Study type: Interventional

Phase 1, single-center, open-label, sequential cohort dose escalation study. This is a 3 + 3 design study involving at least 3 subjects in ascending dose cohorts, with subjects participating up to 10 weeks. The overall study objectives are to evaluate the safety and tolerability of TXA127 in thrombocytopenic subjects with low or intermediate-1 risk MDS. Evaluation of the platelet response and the erythroid and granulocytic responses to TXA127 will provide preliminary efficacy data.

NCT ID: NCT01286038 Terminated - Thrombocytopenia Clinical Trials

Eltrombopag in Myelodysplastic Syndrome (MDS) Patients With Thrombocytopenia

Start date: April 6, 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of eltrombopag in people who have myelodysplastic syndrome (MDS) with thrombocytopenia who have progressed or are resistant to decitabine or azacitidine. (These are the only 2 drugs approved by the U.S. Food and Drug Administration [FDA] which can improve platelet counts). The investigators (the study doctor, study staff, and sponsor) want to find out what effects, good or bad, eltrombopag (study drug) may have on people with low platelet counts due to MDS. The investigators will also be testing how well eltrombopag may work at different doses in these diseases.

NCT ID: NCT01050764 Terminated - Clinical trials for Myelodysplastic Syndrome (MDS)

Haploidentical Allogeneic Transplant With Post-transplant Infusion of Regulatory T-cells

Start date: June 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Patients with hematologic malignancies will receive myeloablative chemotherapy followed by stem cell rescue with bone marrow or hematopoietic peripheral blood stem cells collected by apheresis from a filgrastim- (G-CSF)-mobilized haploidentical related-donor, ie, hematopoietic peripheral blood stem cell transplant (HSCT).

NCT ID: NCT01034657 Terminated - Clinical trials for Myelodysplastic Syndrome (MDS)

LBH589 Alone or in Combination With Erythropoietin Stimulating Agents (ESA) in Patients With Low or Int-1 Risk Myelodysplastic Syndromes (MDS)

GEPARD
Start date: November 2009
Phase: Phase 2
Study type: Interventional

This study assessed the efficacy and safety of LBH589 as single agent and in combination with ESA in red blood cell transfusion-dependent Low and Int-1 MDS patients being either refractory to ESA or with a low probability of response. The study had a non-randomized core phase followed by a randomized phase.

NCT ID: NCT00977132 Terminated - Clinical trials for Myelodysplastic Syndrome MDS

Efficacy and Tolerability of the Combination of Valproic Acid and Lenalidomide in the Treatment of Patients With Myelodysplastic Syndrome

VALENA
Start date: October 2009
Phase: Phase 2
Study type: Interventional

As part of a palliative therapy concept, feasibility, toxicity, and effectiveness of treatment with the combination of Valproic acid and lenalidomide in Myelodysplastic Syndrome patients with a favorable risk profile will be investigated.

NCT ID: NCT00672152 Terminated - Clinical trials for Myelodysplastic Syndrome (MDS)

A Phase I Study of WT1 Peptides to Induce Anti-Leukemia Immune Responses Following Transplantation

WT-1
Start date: June 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and effectiveness of administering Wilms tumor gene 1 (WT1) cancer peptides. Cancer peptides are short pieces of protein that are made in a laboratory to be like the peptides that can be found in cancer. These peptides are intended to be given as a "vaccine" to activate the immune cells in a person to attack his/her cancer. These peptides are mixed with an oily substance called Montanide ISA-51 and a white cell growth factor called Granulocyte-macrophage colony-stimulating factor (GM-CSF) which may help make the immune response stronger.

NCT ID: NCT00666497 Terminated - Clinical trials for Acute Myeloid Leukemia (AML)

Phase 2 Study of Azacitidine (Vidaza) vs MGCD0103 vs Combination in Elderly Subjects With Newly Diagnosed Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS)

Start date: June 2008
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine how effective azacitidine, MGCD0103, and the combination of azacitidine and MGCD0103 are in treating AML or MDS in people over 60 years of age.