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Pancytopenia clinical trials

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NCT ID: NCT02231710 Terminated - Hemoglobinopathies Clinical Trials

Safety Study of Gene Modified Donor T Cell Infusion After Stem Cell Transplant for Non-Malignant Diseases

Start date: February 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine a safe dose of BPX-501 gene modified T cells infused after a haplo-identical stem cell transplant to facilitate engraftment and the safety of Rimiducid (AP1903) on day 7 to prevent GVHD.

NCT ID: NCT01856582 Terminated - Bone Marrow Failure Clinical Trials

CD34+ Stem Cell Infusion to Augment Graft Function

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if infusing additional special donor cells will help to improve graft or immune function in previously transplanted children with immune deficiencies and bone marrow failures.

NCT ID: NCT01596699 Terminated - Metabolic Disease Clinical Trials

Pilot Trial of Clofarabine Added to Standard Busulfan and Fludarabine for Conditioning Prior to Allogeneic Hematopoietic Cell Transplantation

Start date: May 24, 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to find out what effects, good and/or bad, the addition of clofarabine, a new chemotherapy agent, to a standard busulfan and fludarabine conditioning treatment has. The study will also look at what causes some people to have high drug levels of these medications in their body compared to other people that may have low drug levels even if they all receive the same dose of medication.

NCT ID: NCT01050439 Terminated - Lymphoma Clinical Trials

Unrelated Donor Transplant for Malignant and Non-Malignant Disorders

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

Unrelated matched donor (cord blood, bone marrow or peripheral blood) allogeneic stem cell transplantation (UDAlloSCT) with either myeloablative or reduced intensity conditioning will be well tolerated and result in a high degree of engraftment in patients with selected malignant and non malignant disorders.

NCT ID: NCT00968864 Terminated - Clinical trials for Acute Myeloid Leukemia

T-cell Depleted Alternative Donor Transplantation

Start date: August 2009
Phase: Phase 2
Study type: Interventional

The primary purpose is to determine the ability of CD34+ selection and T cell depletion using the CliniMACS® device to prevent severe acute graft-versus-host disease (GVHD) in patients receiving a stem cell transplant from an alternative (unrelated and mismatched related) donor. The secondary objectives include evaluation of engraftment, immune recovery, and post-transplant infections. Patients requiring stem cell transplants for either malignant (cancerous) or non-malignant disease will be included in the study. The recipients will be grouped into one of two groups based on whether the donor is mismatched related (Cohort A) or unrelated (Cohort B). The patient will receive a conditioning regimen including chemotherapy drugs and/or total body irradiation based on the disease for which the transplant is performed.

NCT ID: NCT00228813 Terminated - Clinical trials for Hematologic Malignancies

G-CSF PMRD: Granulocyte Colony Stimulating Factor (G-CSF) Stimulated Bone Marrow and In Vivo T-Cell Depletion in Patients With Hematologic Malignancies or Bone Marrow Failure Syndrome

G-CSF PMRD
Start date: April 2004
Phase: N/A
Study type: Interventional

The purposes of this study are: - To examine the engraftment rate in patients receiving in vivo T-cell-depleted G-CSF stimulated bone marrow from partially mismatched related donors. - To evaluate the incidence and severity of acute and chronic graft-versus-host disease in patients receiving in vivo T-cell-depleted G-CSF stimulated bone marrow from partially mismatched related donors.

NCT ID: NCT00038779 Terminated - Leukemia Clinical Trials

Blood Transplantation for Patients With Hematologic Malignancies or Bone Marrow Failure States

Start date: August 14, 1996
Phase: N/A
Study type: Interventional

The purpose of this study is to assess early treatment failure within 100 days and to assess the effect of this regimen on engraftment, GVHD, immune recovery, relapse of malignancy and survival.