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Clinical trial condition

Hurler-Scheie Syndrome

Explore clinical trials studying Hurler-Scheie Syndrome. Study availability and eligibility vary by location and protocol.

7 public trials 0 recruiting studies
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Hurler-Scheie Syndrome trial results

Completed

A Study of Intrathecal Enzyme Therapy for Cognitive Decline in MPS I

NCT00852358

Conditions
Carbohydrate Metabolism, Inborn Errors, Cognition Disorders, Cognitive Decline, +17 more
Locations
  • Children's Hospital & Research Center Oakland Oakland, California, United States
  • Los Angeles Biomedical Institute at Harbor-UCLA Torrance, California, United States
  • University of Minnesota Minneapolis, Minnesota, United States
View Trial Details
Completed

A Dose-optimization Study of Aldurazyme® (Laronidase) in Patients With Mucopolysaccharidosis I (MPS I) Disease

NCT00144781

Conditions
Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +12 more
Locations
  • Hospital Infantil Joana de Gusmao Florianópolis, Santa Catarina, Brazil
  • Universidade Federal de Minas Gerais Belo Horizonte, Brazil
  • Hospital de Clinical de Porto Alegre Porto Alegre, Brazil
  • Universidade Federal de Sao Paulo São Paulo, Brazil
View Trial Details
Completed

A Study Evaluating the Safety and Pharmacokinetics of Aldurazyme® (Laronidase) in MPS I Patients Less Than 5 Years Old

NCT00146757

Conditions
Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +12 more
Locations
  • Hôpital E. Herriot Lyon, France
  • Johannes Gutenberg Universität Kinderklinik, Mainz, Germany
  • Sophia Children's Hospital Rotterdam, Netherlands
  • Willink Biochemical Genetics Unit Royal Hospital for Children Manchester, United Kingdom
View Trial Details
Completed

Phase 3 Extension Study of the Safety and Efficacy of Aldurazyme® (Laronidase) in Mucopolysaccharidosis I (MPS I) Patients

NCT00146770

Conditions
Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +12 more
Locations
  • University of South Alabama Mobile, Alabama, United States
  • Emory University School of Medicine Atlanta, Georgia, United States
  • University of Rochester Rochester, New York, United States
  • University of North Carolina at Chapel Hill Chapel Hill, North Carolina, United States
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View Trial Details
Completed

A Study Investigating the Relationship Between the Development of Laronidase Antibody and Urinary GAG (Glycosaminoglycan) Levels in Aldurazyme® Treated Patients

NCT00144768

Conditions
Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +12 more
Locations
  • Childrens Hospital Los Angeles Los Angles, California, United States
  • Connecticut Children's Medical Center Hartford, Connecticut, United States
  • Children's Hospital of Wisconsin Milwaukee, Wisconsin, United States
View Trial Details

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