Page 1 of Clinical Trials for "Genetic Diseases, X-Linked", 420 Total Matches
- 1CompletedLast Updated: February 2, 2010Condition(s): X-Linked Lymphoproliferative Disease; Lymphoproliferative Disease; Genetic Diseases, X-Linked
- 2Active, not recruitingLast Updated: July 28, 2011Condition(s): Retinitis Pigmentosa; X-linked Genetic Diseases
- 3Active, not recruitingLast Updated: June 23, 2005Condition(s): X-Linked Agammaglobulinemia; X-Linked Hyper IgM Syndrome; Wiskott-Aldrich Syndrome; Leukocyte Adhesion Deficiency Syndrome
- 4RecruitingLast Updated: February 2, 2012Condition(s): Primary Immune Deficiency Disorders; Common Variable Immunodeficiency; X-linked Agammaglobulinemia; Hyper-IgM Syndrome; Wiskott-Aldrich Syndrome
- 5TerminatedLast Updated: October 14, 2009Condition(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 Syndrome
- 6RecruitingLast Updated: June 24, 2010Condition(s): Disorders of Sex Development; Congenital Adrenal Hyperplasia; Congenital Adrenal Hypoplasia; Adrenal Insufficiency; Mineralocorticoid Deficiency; Intersex
- 7CompletedLast Updated: August 2, 2011Condition(s): Common Variable Immunodeficiency; X-linked Agammaglobulinemia; Autosomal Recessive Agammaglobulinemia
- 8Active, not recruitingLast Updated: June 23, 2005Condition(s): I Cell Disease; Fucosidosis; Globoid Cell Leukodystrophy; Adrenoleukodystrophy; Mannosidosis; Niemann-Pick Disease; Pulmonary Complications; Mucopolysaccharidosis I; Mucopolysaccharidosis VI; Metachromatic Leukodystrophy; Gaucher's Disease; Wolman Disease
- 9CompletedLast Updated: August 29, 2011Condition(s): Fabry Disease
- 10Active, not recruitingLast Updated: March 21, 2012Condition(s): Growth Failure; X-linked Severe Combined Immunodeficiency (XSCID); Growth Hormone Resistence
- 11RecruitingLast Updated: August 22, 2011Condition(s): Duchenne Muscular Dystrophy; Spinal Muscular Atrophy; Congenital Muscular Dystrophy
- 12Not yet recruitingLast Updated: March 15, 2012Condition(s): Duchenne Muscular Dystrophy; Becker Muscular Dystrophy; Dystrophinopathy
- 13CompletedLast Updated: June 23, 2005Condition(s): Hemophilia B; Factor IX Deficiency
- 14RecruitingLast Updated: January 16, 2009Condition(s): Haemophilia A; Haemophilia B
- 15Active, not recruitingLast Updated: December 16, 2011Condition(s): Fabry Disease
- 16RecruitingLast Updated: April 11, 2012Condition(s): Motor Neuron Disease
- 17RecruitingLast Updated: April 18, 2012Condition(s): Duchenne Muscular Dystrophy
- 18Not yet recruitingLast Updated: May 17, 2012Condition(s): Mucopolysaccharidosis II
- 19Enrolling by invitationLast Updated: June 9, 2009Condition(s): Congenital Vertical Talus; Familial Encephalopathy With Neuroserpin Inclusion Bodies; Idiopathic Generalised Epilepsy; Familial Dementia; X-Linked Mental Retardation
- 20Not yet recruitingLast Updated: April 2, 2012Condition(s): Granulomatous Disease, Chronic, X-linked, Variant
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Genetic+Diseases%2C+X-Linked%22
