Hyper-IgM Immunodeficiency Syndrome: Clinical Trials

5 trials for Hyper-IgM Immunodeficiency Syndrome, newest first

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4 completed, 1 recruiting. 5 Phase 2, 2 Phase 1.

By phase and status

PhaseTrialsStatus
Phase 25Completed 4, Recruiting 1
Phase 12Completed 2

Follow Hyper-IgM Immunodeficiency Syndrome: new trials by email Literature Review of Hyper-IgM Immunodeficiency Syndrome trials Research Report on Hyper-IgM Immunodeficiency Syndrome

Trials (filtered) newest first · largest first

All 5 trials

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Hematopoietic Stem Cell Transplantation (HSCT) for Common Variable Immunodeficiency (CVID) and Other Autoimmune Manifestations of Primary Immune Regulatory Disorders (PIRD)
Hematopoietic stem cell transplant (HSCT) - Common Variable Immunodeficiency (CVID), Primary Immune Regulatory Disorder
Phase 2RecruitingPaul Szabolcs252026-05-042026-05-15
Pilot Study Related to the Effect of Clopidogrel on Plasmatic Soluble CD40 Ligand During Systemic Lupus Erythematous
Treatment by clopidogrel - Systemic Lupus Erythematous
Phase 1 / Phase 2CompletedUniversity Hospital, Bordeaux182015-08-192026-05-14
Reduced Intensity Conditioning for Hemophagocytic Syndromes or Selected Primary Immune Deficiencies (BMT CTN 1204)
Hematopoietic Stem Cell Transplant - Hemophagocytic Lymphohistiocytosis, Chronic Active Epstein-Barr Virus Infection
Phase 2CompletedMedical College of Wisconsin472013-12-012022-12-08
Immune Disorder HSCT Protocol
Transplant preparative regimen of alemtuzumab, fludarabine, thiotepa, and melphalan - Immune Deficiency Disorders, Severe Combined Immunodeficiency
Phase 2CompletedWashington University School of Medicine282013-04-292026-10-27
Unrelated Hematopoietic Stem Cell Transplantation(HSCT) for Genetic Diseases of Blood Cells
Hematopoietic stem cell transplantation - Sickle Cell Disease, Thalassemia
Phase 1 / Phase 2CompletedChildren's Hospital Los Angeles252008-08-012016-06-23

Narrower conditions

Granulomatous Disease, Chronic (4)  ·  Chediak-Higashi Syndrome (2)  ·  Common Variable Immunodeficiency (2)  ·  DiGeorge Syndrome (2)  ·  Lymphohistiocytosis, Hemophagocytic (2)  ·  Lymphoproliferative Disorders (2)  ·  Severe Combined Immunodeficiency (2)  ·  Wiskott-Aldrich Syndrome (2)  ·  Anemia (1)  ·  Anemia, Dyserythropoietic, Congenital (1)  ·  Anemia, Sickle Cell (1)  ·  Autoimmune Lymphoproliferative Syndrome (1)  ·  Bruton type agammaglobulinemia (1)  ·  Congenital amegakaryocytic thrombocytopenia (1)

Broader conditions

Blood Protein Disorders (5)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (5)  ·  Dysgammaglobulinemia (5)  ·  Hematologic Diseases (5)  ·  Hemic and Lymphatic Diseases (5)  ·  Primary Immunodeficiency Diseases (5)  ·  Chronic Disease (4)  ·  Disease Attributes (4)  ·  Genetic Diseases, Inborn (4)  ·  Genetic Diseases, X-Linked (4)  ·  Immune System Diseases (4)  ·  Immunologic Deficiency Syndromes (4)  ·  Leukocyte Disorders (4)  ·  Lymphatic Diseases (4)  ·  Pathologic Processes (4)

Interventions

Stem Cell Transplantation (2)  ·  Hematopoietic Stem Cell Transplantation (1)  ·  Melphalan (1)  ·  Thiotepa (1)  ·  fludarabine (1)

Sponsors

Children's Hospital Los Angeles (1)  ·  Medical College of Wisconsin (1)  ·  Paul Szabolcs (1)  ·  University Hospital, Bordeaux (1)  ·  Washington University School of Medicine (1)

Countries

United States (4)  ·  Canada (1)  ·  France (1)

Top investigators

Hisham Abdel-Azim, MD (1)  ·  Mary Horowitz, MD, MS (1)  ·  Paul Szabolcs, MD (1)

Results publications

PMID 29635077, PMID 31599480, PMID 33152483, PMID 37042921

NIH funding

2014 (1), U10HL069294 (1), U24CA076518 (1)