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Myelodysplastic Syndrome (MDS) clinical trials

View clinical trials related to Myelodysplastic Syndrome (MDS).

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NCT ID: NCT00664677 Terminated - Clinical trials for Acute Myeloid Leukemia (AML)

Phase 1 Study of Terameprocol (EM-1421) in Patients With Leukemia

Start date: August 2007
Phase: Phase 1
Study type: Interventional

This study is designed to determine the safety, maximum tolerated dose,dose limiting toxicity of Terameprocol(EM-1421)and determine the pharmacokinetics (clearance from the blood)of Terameprocol(EM-1421)given as intravenous infusion three times a week in patients with leukemia.

NCT ID: NCT00655395 Terminated - Clinical trials for Acute Myeloid Leukemia (AML)

Treatment of Elderly Patients With Acute Myeloid Leukemia (AML) and High Risk Myelodysplastic (MD) Syndrome With Laromustine and Infusional Cytarabine

Start date: March 2008
Phase: Phase 1/Phase 2
Study type: Interventional

- The purpose of the Phase I portion of this study is to evaluate the safety of this combination of medications and to determine the appropriate dose of VNP40101M to be used in combination with infusional cytarabine (araC) in elderly patients with Acute Myeloid Leukemia (AML) and High Risk Myelodysplastic Syndrome (MDS). - The purpose of the Phase II portion of the study is to evaluate the effectiveness (overall response rate) for patients treated with VNP40101M and infusional cytarabine induction therapy.

NCT ID: NCT00542828 Terminated - Clinical trials for Myelodysplastic Syndrome (MDS)

Rabbit Anti-thymocyte Globulin in the Treatment of Patients With Low to Intermediate-1 Risk Myelodysplastic Syndrome

RISE
Start date: October 2007
Phase: Phase 2
Study type: Interventional

This is a Phase II, single-arm, open-label, multinational, multicenter study of rATG in patients with low or intermediate-1 risk MDS who have either failed 1 prior treatment with growth factor(s), hypomethylating agents (5-azacitidine or decitabine), or the antiangiogenic agents lenalidomide or thalidomide, or who have never been treated for MDS (i.e., treatment-naïve patients).

NCT ID: NCT00225992 Terminated - Clinical trials for Myelodysplastic Syndrome (MDS)

Phase II Research Study of Arsenic Trioxide (Trisenox) in Patients With Myelodysplastic Syndrome (MDS)

Start date: February 2004
Phase: Phase 2
Study type: Interventional

In this phase II study besides evaluating for safety, the primary efficacy parameter is to evaluate the incidence of patients who have had a response to Trisenox by evidence of increased blood counts (red, white, or platelets) and/or by decrease or transfusion dependency. The secondary efficacy parameter is the assessment of the tolerability of the new dosing schedule. Arsenic trioxide will be administered intravenously over 1 to 2 hours with a loading dose of 0.30mg/kg for days 1-5 of the first week and then twice weekly for 27 weeks for a total of 28 weeks.