Natural History Study of Children With Metachromatic Leukodystrophy

Shire

Status: Terminated

Conditions: Hereditary Central Nervous System Demyelinating Diseases; Genetic Diseases, Inborn; Lysosomal Storage Diseases; Central Nervous System Diseases; Nervous System Diseases; Sulfatidosis; Metachromatic Leukodystrophy (MLD); Metabolic Diseases; Sphingolipidoses; Metabolic Inborn Brain Diseases; Lipid Metabolism Disorders; Metabolism, Inborn Errors; Demyelinating Diseases; Brain Diseases

Study type: Observational

Funder types: Industry

Identifiers

NCT01963650

HGT-MLD-092

Details and patient eligibility

About

The purpose of this study is evaluate the natural course of disease progression related to gross motor function in children with metachromatic leukodystrophy (MLD).

Full description

Metachromatic leukodystrophy (MLD) is an inherited, autosomal recessive disorder of lipid metabolism characterized by deficient activity of the lysosomal enzyme, arylsulfatase A (ASA). MLD is a rare genetic disease that occurs in most parts of the world. The estimated overall incidence of the disease in the western world is approximately 1 in 100,000 live births.

This study is a multicenter, observational, longitudinal study that plans to enroll up to 30 patients with onset of MLD-related signs and symptoms prior to 30 months of age and who are less than 12 years of age. Patients will participate in this study for approximately 114 weeks (Screening through Follow-up) and will be assessed at defined intervals for disease status.

Enrollment: 1 patient

Sex: All

Ages: Under 12 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Confirmed diagnosis of MLD by both:

   • arylsulfatase A (ASA) deficiency by assay in leukocytes AND
   • elevated sulfatide in urine

2. Appearance of the first symptoms of disease at or before 30 months of age.

3. A GMFM-88 total (percent) score greater than or equal to 40 at the screening examination.

4. The patient is less than 12 years of age at the time of enrollment.

5. The patient and his/her parent or legally authorized representative(s) must have the ability to comply with the clinical protocol.

6. Patient's parent or legally authorized representative(s) must provide written informed consent prior to performing any study-related activities. Study-related activities are any procedures that would not have been performed during normal management of the patient.

Exclusion criteria

1. History of hematopoietic stem cell transplantation.
2. The patient has any known or suspected hypersensitivity to agents used for anesthesia or is thought to be at an unacceptably high risk for associated potential complications of airway compromise or other conditions.
3. Any other medical condition, serious intercurrent illness, or extenuating circumstance that, in the opinion of the Investigator, would preclude participation in the study.
4. The patient is enrolled in another clinical study that involves the use of any investigational product (drug or device) within 30 days prior to study enrollment or at any time during the study.

Trial design

1 participants in 1 patient group

No treatment