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MDS clinical trials

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NCT ID: NCT00636909 Completed - MULTIPLE MYELOMA Clinical Trials

Nonmyeloablative Allo SCT for the Treatment of Hematologic Disorders

MINI HEME
Start date: July 1999
Phase: Phase 2
Study type: Interventional

The purpose of this study is to provide allogeneic stem cell transplantation to patients who have not traditionally undergone this procedure because of it high incidence of treatment related side effects. We hope to decrease these side effects by decreasing the chemotherapy dose prior to transplant (non-myeloablative, smaller dose of chemotherapy given so bone marrow is not completely eliminated) and by using donated stem cells to treat cancer of the blood.

NCT ID: NCT00614523 Completed - Clinical trials for Myelodysplastic Syndromes

Romiplostim Treatment of Thrombocytopenia in Subjects With Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS)

Start date: July 21, 2008
Phase: Phase 2
Study type: Interventional

The Data Monitoring Committee (DMC) for study 20060198 recommended that all subjects discontinue treatment of study drug and continue to be followed for long term follow-up. Amgen adopted the DMC recommendation.

NCT ID: NCT00530218 Completed - Multiple Myeloma Clinical Trials

Ganciclovir by Infusion and by Mouth in Treating Patients With Cytomegalovirus After Donor Bone Marrow Transplant

Start date: March 1999
Phase: Phase 2
Study type: Interventional

RATIONALE: Antiviral drugs, such as ganciclovir, act against viruses. Giving ganciclovir by infusion and then by mouth may be effective treatment for cytomegalovirus that has become active after donor bone marrow transplant. PURPOSE: This phase II trial is studying how well giving ganciclovir by infusion and by mouth works in treating patients with cytomegalovirus after donor bone marrow transplant.

NCT ID: NCT00493571 Completed - Clinical trials for Myelodysplastic Syndromes

Phase I Study of Gimatecan in Patients With Myelodysplastic Syndromes

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

The goal of this clinical research study is to find the highest tolerable dose of gimatecan that can be given to treat myelodysplastic syndrome (MDS).

NCT ID: NCT00472290 Completed - Clinical trials for Myelodysplastic Syndromes

Evaluating the Safety of Long Term Dosing of Romiplostim (Formerly AMG 531) in Thrombocytopenic Subjects With Myelodysplastic Syndromes (MDS)

Start date: April 1, 2007
Phase: N/A
Study type: Interventional

This is an open label extension study of romiplostim for treatment of thrombocytopenia (platelet count ≤ 50 x 10^9/L) in MDS subjects. The study is designed to assess the long-term safety of treatment with romiplostim, as measured by incidence of overall adverse events, the incidence of bleeding events, the utilization of platelet transfusions, and the duration of platelet response. The study will further describe the time to disease progression to acute myeloid leukemia (AML) and survival.

NCT ID: NCT00462761 Completed - Leukemia Clinical Trials

A Phase I Study of AC220 in Patients With Relapsed/Refractory Acute Myeloid Leukemia Regardless of FLT3 Status

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

Patients received oral AC220 daily for 14 days to study the side effects, tolerability and best dose for treating relapsed or refractory acute myeloid leukemia, regardless of FLT3 status.

NCT ID: NCT00321711 Completed - Clinical trials for Myelodysplastic Syndromes

Determination of Safe and Effective Dose of Romiplostim (AMG 531) in Subjects With Myelodysplastic Syndrome (MDS)Receiving Hypomethylating Agents

Start date: October 1, 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of Romiplostim (AMG 531) on the incidence of clinically significant thrombocytopenic events (grade 3 or 4 and/or receipt of platelet transfusions) in subjects with low or intermediate risk Myelodysplastic Syndrome (MDS) receiving hypomethylating agents. It is hypothesized that Romiplostim administration, at the appropriate dose and schedule, will result in reduction in the incidence of clinically significant thrombocytopenic events in low or intermediate risk MDS subjects receiving hypomethylating agents.

NCT ID: NCT00309842 Completed - Multiple Myeloma Clinical Trials

Myeloablative Umbilical Cord Blood Transplantation in Hematological Diseases

Start date: July 28, 2005
Phase: Phase 2
Study type: Interventional

RATIONALE: Giving chemotherapy drugs, such as fludarabine and cyclophosphamide, and total-body irradiation before a donor umbilical cord blood stem cell transplant helps stop the growth of cancer cells and prepares the patient's bone marrow for the stem cells. When the healthy stem 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. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells. Giving cyclosporine and mycophenolate mofetil may stop this from happening. PURPOSE: This phase II trial is studying how well giving fludarabine and cyclophosphamide together with total-body irradiation works in treating patients who are undergoing an umbilical cord blood transplant for hematologic cancer.

NCT ID: NCT00303472 Completed - Clinical trials for Myelodysplastic Syndromes

Determination of Safe Dose of Romiplostim (AMG 531) in Patients With Myelodysplastic Syndromes (MDS)

Start date: February 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of romiplostim in thrombocytopenic patients with low or Intermediate-1 risk MDS. In addition, the study will evaluate the platelet response to romiplostim.

NCT ID: NCT00185692 Completed - Leukemia Clinical Trials

Allogeneic Transplantation From Related Haploidentical Donors

Start date: August 2000
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the feasibility and safety of transplanting CD34+ selected hematopoietic cells from a haploidentical related donor following a nonmyeloablative regimen of total lymphoid irradiation (TLI) and antithymocyte globulin (ATG).