Study of Inborn Errors of Cholesterol Synthesis and Related Disorders
Condition(s):Lysosomal Storage Disease; Cholesterol MetabolismLast Updated:March 15, 2024Recruiting
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Condition(s):Lysosomal Storage Disease; Cholesterol MetabolismLast Updated:March 15, 2024Recruiting
Condition(s):Lysosomal Storage Diseases; Metachromatic LeukodystrophyLast Updated:January 18, 2024Active, not recruiting
Condition(s):Lysosomal Storage Disease; Metachromatic LeukodystrophyLast Updated:November 28, 2023Active, not recruiting
Condition(s):Lysosomal Storage Disease; Peroxisomal DisorderLast Updated:December 5, 2017Completed
Condition(s):Lysosomal Storage Disease; Metachromatic LeukodystrophyLast Updated:November 24, 2023Active, not recruiting
Condition(s):Fabry Disease; Gaucher Disease; Niemann-Pick Disease, Type C; Lysosomal Storage DiseasesLast Updated:June 7, 2021Withdrawn
Condition(s):Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis IV A; Mucopolysaccharidosis VI; Mucopolysaccharidosis VII; Pompe Disease Infantile-Onset; Neuronopathic Gaucher Disease; Wolman DiseaseLast Updated:December 12, 2023Recruiting
Condition(s):Mucopolysaccharidosis Type I (MPS I); Mucopolysaccharidosis Type II (MPS II); Mucopolysaccharidosis Type III (MPS III); Mucopolysaccharidosis Type VI (MPS VI); Krabbe DiseaseLast Updated:October 4, 2019Completed
Condition(s):Aspartylglucosaminuria; Aspartylglucosamidase (AGA) Deficiency; Lysosomal Storage DiseasesLast Updated:April 12, 2022Terminated
Condition(s):MPS I; MPS II; MPS IVA; MPS VI; Mps VII; Gaucher Disease, Type 2; Gaucher Disease, Type 3; Pompe Disease Infantile-Onset; Wolman DiseaseLast Updated:September 21, 2023Recruiting
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