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Mutation of the BTK Gene and Genotype-phenotype Correlation of Chinese Patients With X-Linked Agammaglobulinemia
Condition(s):Agammaglobulinemia, BTKLast Updated:September 9, 2014Unknown status
X-linked Agammaglobulinemia: 13 Clinical Trials, Page 1 of 2
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Hyaluronic Acid Filler IMD1 Basic for Correction of Nasolabial Folds
Condition(s):Nasolabial FoldsLast Updated:February 7, 2008Completed
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Assessment of Immunogenicity of Zostavax® in Patients With Antibody Deficiency 60 Years of Age and Older
Condition(s):Common Variable Immune Deficiency; Specific Antibody Deficiency; X-linked AgammaglobulinemiaLast Updated:May 31, 2018Terminated
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Study of Subcutaneous Immune Globulin in Patients Requiring IgG Replacement Therapy
Condition(s):Common Variable Immunodeficiency; X-linked Agammaglobulinemia; Autosomal Recessive AgammaglobulinemiaLast Updated:September 1, 2011Completed
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Pharmacokinetics (PK) and Safety of Subgam-VF in Primary Immunodeficiency Diseases
Condition(s):Primary Immune Deficiency Disorders; Common Variable Immunodeficiency; X-linked Agammaglobulinaemia; Hyperimmunoglobulin M SyndromeLast Updated:September 12, 2018Completed
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Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders
Condition(s):X-Linked Agammaglobulinemia; X-Linked Hyper IgM Syndrome; Wiskott-Aldrich Syndrome; Leukocyte Adhesion Deficiency SyndromeLast Updated:June 24, 2005Unknown status
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Bioequivalence Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Gammaplex® 10 and Gammaplex® 5% in Primary Immunodeficiency Diseases
Condition(s):Primary Immune Deficiency Disorders; Common Variable Immunodeficiency; X-linked Agammaglobulinaemia; Hyper-IgM SyndromeLast Updated:March 29, 2017Completed
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A Study to Find Out How Safe and Effective Gammaplex® is in Young People With Primary Immunodeficiency
Condition(s):Primary Immune Deficiency Disorders; Common Variable Immunodeficiency; X-linked Agammaglobulinemia; Hyper-IgM Syndrome; Wiskott-Aldrich SyndromeLast Updated:December 23, 2014Completed
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COVID-19 Vaccine Responses in PIDD Subjects
Condition(s):X-linked Agammaglobulinemia; XLA; Primary Immune Deficiency; CVID; Common Variable Immunodeficiency; Primary Antibody Deficiencies; Secondary HypogammaglobulinemiaLast Updated:April 11, 2022Recruiting
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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