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Myelofibrosis clinical trials

View clinical trials related to Myelofibrosis.

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NCT ID: NCT00475020 Completed - Myelofibrosis Clinical Trials

Allogeneic Stem Cell Transplantation for Myelofibrosis and Myelodysplastic Syndrome

Start date: January 4, 2006
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if using a combination of fludarabine, busulfan, and antithymocyte globulin (ATG) can help to control myelofibrosis or myelodysplastic syndrome in patients receiving a bone marrow or blood stem cell transplant. The safety of these drugs will also be studied.

NCT ID: NCT00463385 Completed - Myelofibrosis Clinical Trials

A Phase II Study of Pomalidomide in Myelofibrosis With Myeloid Metaplasia

Start date: April 1, 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety of and to select a treatment regimen of pomalidomide (CC-4047) either as single-agent or in combination with prednisone to study further in patients with myelofibrosis with myeloid metaplasia (MMM).

NCT ID: NCT00360035 Completed - Myelofibrosis Clinical Trials

Safety and Efficacy of Obatoclax Mesylate (GX15-070MS) in the Treatment of Myelofibrosis With Myeloid Metaplasia

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

Defects in the apoptotic process can lead to the onset of cancer by allowing cells to grow unchecked when an oncogenic signal is present. Obatoclax is designed to restore apoptosis through inhibition of the Bcl-2 family of proteins, thereby reinstating the natural process of cell death that is often inhibited in cancer cells.

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: NCT00352794 Completed - Myelofibrosis Clinical Trials

Lenalidomide for Patients With Myelofibrosis (MF)

Start date: July 7, 2006
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if lenalidomide in combination with prednisone can help to control myelofibrosis. The safety of lenalidomide and prednisone for the treatment of myelofibrosis will also be studied.

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: NCT00287261 Completed - Myelofibrosis Clinical Trials

A Trial of Zoledronic Acid in Patients With Myelofibrosis With Myeloid Metaplasia (MMM)

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

In this trial, the question is addressed if zoledronic acid (Zometa, Novartis Pharma)could be of clinical benefit for patients with myelofibrosis and myeloid metaplasia (MMM).

NCT ID: NCT00255346 Completed - Clinical trials for Acute Myeloid Leukemia

Dasatinib as Therapy for Myeloproliferative Disorders (MPDs)

Start date: November 15, 2005
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if dasatinib can help to control myeloproliferative disorders. The safety and tolerability of dasatinib will also be studied.

NCT ID: NCT00235391 Completed - Sickle Cell Disease Clinical Trials

Expanded Access of Deferasirox to Patients With Congenital Disorders of Red Blood Cells and Chronic Iron Overload

Start date: October 2005
Phase: Phase 3
Study type: Interventional

This is an open-label, non-randomized, multi-center trial designed to provide expanded access of deferasirox to patients with congenital disorders of red blood cells and chronic iron overload from blood transfusions who cannot adequately be treated with locally approved iron chelators.

NCT ID: NCT00136409 Completed - Clinical trials for Chronic Myelomonocytic Leukemia

A Study of Gleevec in Patients With Idiopathic Myelofibrosis or Chronic Myelomonocytic Leukemia (CMML)

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

The purpose of this study is to determine the effects (good and bad) of Gleevec in patients with BCR-negative myeloproliferative disorders including myelofibrosis with myeloid metaplasia and chronic myelomonocytic leukemia.