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Myelodysplasia clinical trials

View clinical trials related to Myelodysplasia.

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NCT ID: NCT00580242 Completed - Myelodysplasia Clinical Trials

A Phase 1 Dose Escalating Trial of Bortezomib in Combination With Lenalidomide in Patients With Myelodysplasia

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

This study proposes using bortezomib in cohorts of 3-6 patients at the doses of 0.7, 1, and 1.3 mg/m2 on days 1, 4, 8, and 11 to determine the MTD in combination with lenalidomide 10 mg a day, for 21 days of a 28 day treatment cycle for patients with myelodysplastic syndrome.

NCT ID: NCT00580034 Completed - Lymphoma Clinical Trials

Allo Non-Myeloablative SCT Utilizing Mis-Matched Family Member Stem Cells Purged Using Campath

Start date: February 2003
Phase: Phase 2
Study type: Interventional

Allogeneic transplantation is used to treat many malignant and non-malignant diseases, though the potential toxicities of the procedure remain high. We and others have shown that a less toxic preparative regimen allows reliable allogeneic engraftment for allogeneic transplantation. The primary purpose of this treatment trial is to follow patients undergoing allogeneic transplantation for long term outcomes. The regimen used has been tested in our prior phase I / II trial which has completed accrual. The issues of engraftment and rate of graft versus host disease have been answered and our success has led to this regimen being a standard approach for less toxic allogeneic therapy.

NCT ID: NCT00578942 Completed - Lymphoma Clinical Trials

Allo Non-myeloablative SCT Utilizing Matched Family Member Stem Cells Purged Using Campath

Start date: May 2005
Phase: Phase 2
Study type: Interventional

Allogeneic transplantation is used to treat many malignant and non-malignant diseases, though the potential toxicities of the procedure remain high. We and others have shown that a less toxic preparative regimen allows reliable allogeneic engraftment for allogeneic transplantation. The primary purpose of this treatment trial is to follow subjects undergoing allogeneic transplantation for long term outcomes. The regimen used has been tested in our prior phase I / II trial which has completed accrual. The issues of engraftment and rate of graft versus host disease have been answered and our success has led to this regimen being a standard approach for less toxic allogeneic therapy.

NCT ID: NCT00516152 Completed - Multiple Myeloma Clinical Trials

Phase II Study Evaluating Busulfan and Fludarabine as Preparative Therapy in Adults With Hematopoietic Disorders Undergoing MUD SCT

Start date: November 2002
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess the safety and efficacy of performing unrelated stem cell transplants using intravenous busulfan and fludarabine as preparative therapy and tacrolimus plus methotrexate as the GVHD prophylaxis regimen. The goal is to demonstrate safety, aiming for a transplant related mortality rate (TRM) of < or equal to 40% at 100 days. A TRM of > or equal to 60% will be considered unacceptable. Another goal is to demonstrate efficacy by showing and overall survival of >40% at 1-year following transplant.

NCT ID: NCT00513175 Completed - Multiple Myeloma Clinical Trials

Non-Myeloablative Allogeneic Stem Cell Transplantation With Matched Unrelated Donors for Treatment of Hematologic Malignancies, Renal Cell Carcinoma, and Aplastic Anemia

Start date: October 2001
Phase: N/A
Study type: Observational

The primary objective of this study is to examine transplant related mortality (TRM) at 100 days <30%. A TRM of >50% is considered unacceptable. This study also seeks a TRM at 12 months that is <50%, engraftment >90% (defined as donor cells >80% at 6 months), and 1 year overall survival >50%.

NCT ID: NCT00511537 Completed - Lymphoma Clinical Trials

Unrelated Stem Cell Transplantation for Adults With Hematopoietic Disorders

Start date: January 1999
Phase: N/A
Study type: Observational

This study performs HLA matched stem cell transplantation from unrelated donors in adults who require stem cell transplantation but do not have a matched related donor available. The incidence of graft-versus-host disease in unrelated stem cell transplantation is recorded. This study also monitors the activity and toxicity of total body irradiation and cyclosphosphamide followed by stem cell transplantation from matched unrelated donors.

NCT ID: NCT00506402 Completed - Clinical trials for Hematological Malignancies

A Phase 1 Study of MKC-1 in Patients With Refractory Hematologic Malignancies

Start date: November 2006
Phase: Phase 1
Study type: Interventional

The main objectives of this study are to evaluate the side effects of MKC-1 and to determine a safe dose of MKC-1 for future studies in patients with hematological malignancies

NCT ID: NCT00354120 Completed - Clinical trials for Chronic Myeloid Leukemia

Thymoglobuline Versus Alemtuzumab in Patients Undergoing Allogeneic Transplant

GLOBAL
Start date: March 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to compare Reduced Intensity Conditioning protocols containing either Thymoglobuline or Alemtuzumab in patients undergoing allogeneic transplant from voluntary unrelated donors.

NCT ID: NCT00195533 Completed - Lymphoma Clinical Trials

Study Comparing Piperacillin-tazobactam Versus Piperacillin-tazobactam Plus Glycopeptide in Neutropenic Patients

Start date: July 2001
Phase: Phase 4
Study type: Observational

The aim of this study is to compare the efficacy and tolerance of piperacillin-tazobactam versus piperacillin-tazobactam plus glycopeptide as initial empiric antibiotic treatment for fever in neutropenic patients. Study of consecutive cohorts(2). First the patients will be included in the monotherapy branch until completing the predicted number of cases. When this happens, the Coordinating Center will communicate it to the participant centers and from then the patients will be included in the combined therapy.

NCT ID: NCT00136422 Completed - Clinical trials for Acute Myelogenous Leukemia

Study of Vaccination With Autologous Acute Myeloblastic Leukemia Cells in Patients With Advanced Myelodysplasia or Acute Myelogenous Leukemia

Start date: January 2000
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the safety of a new investigational acute myeloblastic leukemia (AML) vaccine and see what effects (good and bad) it has on patients with advanced myelodysplasia or acute myelogenous leukemia.