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Genetic Studies of X-linked Lymphoproliferative Disease
Condition(s):X-Linked Lymphoproliferative Disease; Lymphoproliferative Disease; Genetic Diseases, X-LinkedLast Updated:July 2, 2017Completed
X-linked Lymphoproliferative Syndrome: 13 Clinical Trials, Page 1 of 2
Hide Studies Not Open or Pending
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Pilot Study of Unrelated Donor Hematopoietic Stem Cell Transplantation in Patients With Life Threatening Hemophagocytic Disorders
Condition(s):Chediak-Higashi Syndrome; Graft Versus Host Disease; X-Linked Lymphoproliferative Syndrome; Familial Erythrophagocytic Lymphohistiocytosis; Hemophagocytic Lymphohistiocytosis; Virus-Associated Hemophagocytic SyndromeLast Updated:June 24, 2005Unknown status
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Allogeneic Bone Marrow Transplantation in Patients With Primary Immunodeficiencies
Condition(s):Immunologic Deficiency Syndromes; Chediak-Higashi Syndrome; Common Variable Immunodeficiency; Graft Versus Host Disease; X-Linked Lymphoproliferative Syndrome; Familial Erythrophagocytic Lymphohistiocytosis; Hemophagocytic Lymphohistiocytosis; X-linked Agammaglobulinemia; Wiskott-Aldrich Syndrome; Chronic Granulomatous Disease; X-linked Hyper IgM Syndrome; Severe Combined Immunodeficiency; Leukocyte Adhesion Deficiency Syndrome; Virus-Associated Hemophagocytic SyndromeLast Updated:October 15, 2009Terminated
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Immune Disorder HSCT Protocol
Condition(s):Immune Deficiency Disorders; Severe Combined Immunodeficiency; Chronic Granulomatous Disease; X-linked Agammaglobulinemia; Wiskott-Aldrich Syndrome; Hyper-IgM; DiGeorge Syndrome; Chediak-Higashi Syndrome; Common Variable Immune Deficiency; Immune Dysregulatory Disorders; Hemophagocytic Lymphohistiocytosis; IPEX; Autoimmune Lymphoproliferative Syndrome; X-linked Lymphoproliferative SyndromeLast Updated:March 26, 2019Recruiting
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Administration of Donor T Cells With the Caspase-9 Suicide Gene
Condition(s):Acute Lymphoblastic Leukemia; Myelodysplastic Syndrome; Acute Myeloid Leukemia; Chronic Myelogenous Leukemia; Non Hodgkin Lymphoma; Hemophagocytic Lymphohistiocytosis; Familial Hemophagocytic Lymphohistiocytosis; Hemophagocytic Syndrome; Epstein Barr Virus Infection; X-linked Lymphoproliferative DiseaseLast Updated:October 9, 2019Active, not recruiting
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Stem Cell Transplant for Immunologic or Histiocytic Disorders
Condition(s):Hemophagocytic Lymphohistiocytosis; X-Linked Lymphoproliferative Disorders; Chediak-Higashi Syndrome; Griscelli Syndrome; Immunologic Deficiency Syndromes; Langerhans-Cell HistiocytosisLast Updated:December 28, 2017Completed
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T Cell Depletion for Recipients of HLA Haploidentical Related Donor Stem Cell Grafts
Condition(s):Acute Lymphoblastic Leukemia; Non Hodgkins Lymphoma; Myelodysplastic Syndrome; Acute Myeloid Leukemia; Chronic Myelogenous Leukemia; Hemophagocytic Lymphohistiocytosis (HLH); Familial Hemophagocytic Lymphohistiocytosis (FLH); Viral-associated Hemophagocytic Syndrome (VAHS); X-linked Lymphoproliferative Disease (XLP)Last Updated:January 21, 2020Completed
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T-Cell Depletion and Stem Cell Transplant for Immune Deficiencies and Histiocytic Disorders
Condition(s):Hemophagocytic Lymphohistiocytosis; X-Linked Lymphoproliferative Disorders; Chediak-Higashi Syndrome; Griscelli Syndrome; Immunologic Diseases; Langerhans-Cell Histiocytosis; Hematologic DiseasesLast Updated:January 23, 2018Terminated
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Conditioning Regimen for Allogeneic Hematopoietic Stem-Cell Transplantation
Condition(s):Bone Marrow Failure Syndrome; Thalassemia; Sickle Cell Disease; Diamond Blackfan Anemia; Acquired Neutropenia in Newborn; Acquired Anemia Hemolytic; Acquired Thrombocytopenia; Hemophagocytic Lymphohistiocytoses; Wiskott-Aldrich Syndrome; Chronic Granulomatous Disease; Common Variable Immunodeficiency; X-linked Lymphoproliferative Disease; Severe Combined Immunodeficiency; Hurler Syndrome; Mannosidosis; AdrenoleukodystrophyLast Updated:January 28, 2020Recruiting
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Allogeneic Hematopoietic Stem Cell Transplant for Patients With Primary Immune Deficiencies
Condition(s):SCID; Omenn’s Syndrome; Reticular Dysgenesis; Wiskott-Aldrich Syndrome; Bare Lymphocyte Syndrome; Common Variable Immunodeficiency; Chronic Granulomatous Disease; CD40 Ligand Deficiency; Hyper IgM Syndrome; X-linked Lymphoproliferative Disease; Hemophagocytic Lymphohistiocytosis; Griscelli Syndrome; Chediak-Higashi Syndrome; Langerhan’s Cell HistiocytosisLast Updated:January 7, 2020Recruiting