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Found 64 clinical trials
Hematopoietic Stem Cell Transplantation in the Treatment of Infant Leukemia

RATIONALE: Giving chemotherapy, such as busulfan, fludarabine, and melphalan, before a donor umbilical cord blood stem cell transplant helps stop the growth of abnormal or cancer cells and

bone marrow procedure
stem cell transplantation
wbc count
combination chemotherapy
cell transplantation
  • 37 views
  • 22 Mar, 2022
  • 1 location
Olaparib Combined With High-Dose Chemotherapy for Refractory Lymphomas

treatment and are undergoing stem cell transplant. Drugs used in chemotherapy, such as olaparib, vorinostat, gemcitabine, busulfan, and melphalan, work in different ways to stop the growth of cancer cells

gemcitabine
salvage therapy
tumor cells
high-dose chemotherapy
hysterectomy
  • 2 views
  • 16 Oct, 2022
  • 1 location
Decitabine Plus mBU/CY for High Risk Acute Leukemia With MRD Pre-HSCT

to examine the efficacy of combining decitabine with modified busulfan and cyclophosphamide (mBU/CY) as a preparative regimen for allo-HSCT in patients with very high-risk AL and detectable MRD pre

cell transplantation
minimal residual disease
decitabine
busulfan
ara-c
  • 2 views
  • 01 Mar, 2022
  • 1 location
Autologous Gene Therapy for Artemis-Deficient SCID

-inactivating lentiviral vector that contains a normal copy of the DCLRE1C gene. Prior to the infusion they will receive sub-ablative, dose-targeted busulfan conditioning. The study will investigate if the

cell transplantation
igiv
immune globulin
busulfan
bone marrow procedure
  • 0 views
  • 10 Mar, 2022
  • 1 location
Gene Transfer for X-Linked Severe Combined Immunodeficiency in Newly Diagnosed Infants (LVXSCID-ND)

SCID-X1 is a genetic disorder of blood cells caused by DNA changes in a gene that is required for the normal development of the human immune system. The purpose of this study is to determine if a new method, called lentiviral gene transfer, can be used to treat SCID-X1. This …

  • 26 views
  • 25 Mar, 2022
  • 3 locations
Alpha/Beta T and CD19+ Depleted Peripheral Stem Cells for Patients With Primary Immunodeficiencies

This is a Phase II trial to determine the ability of a reduced intensity conditioning regimen to allow successful engraftment with alpha/beta T and CD19+ depleted peripheral stem cell grafts from unrelated or partially matched related donors. There are two conditioning regimens depending upon patient diagnosis and age.

transplant conditioning
allogeneic hematopoietic stem cell transplant
wiskott-aldrich syndrome
shortening fraction
histiocytosis
  • 3 views
  • 25 Feb, 2022
  • 1 location
Haploidentical Transplantation With Pre-Transplant Immunosuppressive Therapy for Patients With Sickle Cell Disease

This is a study to evaluate the safety and toxicity of a treatment regimen consisting of 2 cycles of pre-transplant immunosuppressive therapy followed by myeloablative preparative regimen and allogeneic hematopoietic stem cell transplantation from a haploidentical donor in patients with sickle cell disease. The overall goal of this study is …

chest syndrome
cell transplantation
blood transfusion
hydroxyurea
stroke
  • 14 views
  • 05 Jul, 2022
  • 1 location
A Phase II Randomized Controlled Trial Comparing GVHD-Reduction Strategies for Allogeneic Peripheral Blood Transplantation (PBSCT) for Patients With Acute Leukemia or Myelodysplastic Syndrome: Selective Depletion of CD45RA+ Naïve T Cells (TND) vs. Post-Transplantation Cyclophosphamide (PTCy)

This phase II trial investigates two strategies and how well they work for the reduction of graft versus host disease in patients with acute leukemia or MDS in remission. Giving chemotherapy and total-body irradiation before a donor peripheral blood stem cell transplant helps stop the growth of cells in the …

remission
graft versus host disease
sirolimus
antithymocyte globulin
blood cell count
  • 3 views
  • 24 Oct, 2022
  • 2 locations
High Dose Peripheral Blood Stem Cell Transplantation With Post Transplant Cyclophosphamide for Patients With Chronic Granulomatous Disease

Chronic granulomatous disease (CGD) affects white blood cell function. Currently, the only curative treatment is bone marrow transplant to replace the abnormal stem cells with new ones (donor cells) capable of making a normal immune system. Transplant problems include graft versus host disease (GvHD) and graft rejection. With GvHD, donor …

  • 3 views
  • 20 Oct, 2022
  • 1 location
A Phase II Study of Allogeneic Hematopoietic Stem Cell Transplant for Subjects With VEXAS (Vacuoles, E1 Enzyme, X-linked, Autoinflammatory, Somatic) Syndrome

Background Allogeneic hematopoietic stem cell transplant involves taking blood stem cells from a donor and giving them to a recipient. The transplants are used to treat certain diseases and cancers. Researchers want to see if the transplant can treat VEXAS Syndrome. Objective To see if stem cell transplants can be …

mycophenolate mofetil
cyclophosphamide
total body irradiation
allogeneic hematopoietic stem cell transplant
busulfan
  • 0 views
  • 21 Oct, 2022
  • 1 location