Page 1 of Clinical Trials for "Mannosidase Deficiency Diseases", 8 Total Matches
- 1CompletedLast Updated: February 5, 2010Condition(s): Alpha Mannosidosis
- 2CompletedLast Updated: May 6, 2011Condition(s): Alpha Mannosidosis
- 3Active, not recruitingLast Updated: June 9, 2011Condition(s): Alpha Mannosidosis
- 4CompletedLast Updated: July 2, 2010Condition(s): Mucopolysaccharidosis I; Mucopolysaccharidosis VI; Mannosidosis; Mucolipidosis Type II (I-cell Disease)
- 5Active, 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
- 6RecruitingLast Updated: April 4, 2012Condition(s): Mucopolysaccharidosis; Hurler Syndrome; Hunter Syndrome; Maroteaux-Lamy Syndrome; Sly Syndrome; Alpha Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Adrenoleukodystrophy (ALD); Globoid Cell Leukodystrophy (GLD); Krabbe Disease; Metachromatic Leukodystrophy (MLD); Sphingolipidoses; Peroxisomal Disorders
- 7TerminatedLast Updated: July 27, 2011Condition(s): Hurler's Syndrome; Maroteaux-Lamy Syndrome; Sly Syndrome; Alpha Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Sphingolipidoses; Krabbe Disease; Wolman's Disease; Niemann-Pick Disease Type B; Niemann-Pick Disease, Type C
- 8SuspendedLast Updated: January 10, 2011Condition(s): Inherited Metabolic Diseases; Lysosomal Storage Disease; Peroxisomal Storage Diseases; Inborn Errors of Metabolism; Mucopolysaccharidosis
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The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Mannosidase+Deficiency+Diseases%22
