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Clinical trial condition

Hereditary Central Nervous System Demyelinating Diseases

Explore clinical trials studying Hereditary Central Nervous System Demyelinating Diseases. Study availability and eligibility vary by location and protocol.

82 public trials 21 recruiting studies
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Hereditary Central Nervous System Demyelinating Diseases trial results

Active, not recruiting

Early Check: Expanded Screening in Newborns

NCT03655223

Conditions
17 Alpha-Hydroxylase Deficiency, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, +456 more
Locations
  • RTI International Research Triangle Park, North Carolina, United States
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Completed

A Study of Intrathecal SHP611 in Children With Metachromatic Leukodystrophy

NCT03771898

Conditions
Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations
  • Los Angeles Biomedical Research Institute at Harbor-UCLA Torrance, California, United States
  • Childrens Hospital Colorado Aurora, Colorado, United States
  • Rare Disease Research, LLC Atlanta, Georgia, United States
  • Ann & Robert H. Lurie Children's Hospital of Chicago Chicago, Illinois, United States
View all 30 locations
View Trial Details
Completed

An Efficacy and Safety Study of HGT-1110 in Participants With Metachromatic Leukodystrophy

NCT01887938

Conditions
Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +19 more
Locations
  • The Children's Hospital at Westmead Westmead, Australia
  • Hospital de Clinicas de Porto Alegre Porto Alegre, Brazil
  • Detska Interni Klinika, Lf Mu A Fn Brno Brno, Czechia
  • Rigshospitalet Copenhagen, Denmark
View all 15 locations
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