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

NACompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

June 30, 2009

Primary Completion Date

April 30, 2015

Study Completion Date

April 30, 2015

Conditions
Cognitive DeclineMucopolysaccharidosis IHurler-Scheie SyndromeScheie SyndromeLysosomal Storage Disease
Interventions
DRUG

laronidase

For the treatment group, intrathecal rhIDU injections will consist of 3 cc of Aldurazyme® (laronidase) (approximately 1.74 mg) diluted with 6 cc of Elliotts B® solution for a total injection of 9 cc. The diluted enzyme will be administered via a lumbar puncture (IT) on day 0 after baseline assessments. IT injections will be repeated on days 30, 60, and 90. The subsequent doses will be administered at 3-month intervals for a total of 10 doses during the two-year period. Control patients will not receive treatment, lumbar puncture, or placebo, but will undergo all other study procedures and assessments during year one. Control patients will then enter a treatment phase consisting of four IT doses at 3-month intervals.

Trial Locations (3)

55455

University of Minnesota, Minneapolis

90502

Los Angeles Biomedical Institute at Harbor-UCLA, Torrance

94609-1809

Children's Hospital & Research Center Oakland, Oakland

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

The Ryan Foundation

OTHER

collaborator

BioMarin Pharmaceutical

INDUSTRY

collaborator

Rare Diseases Clinical Research Network

NETWORK

collaborator

National Center for Advancing Translational Sciences (NCATS)

NIH

collaborator

National Institute of Neurological Disorders and Stroke (NINDS)

NIH

collaborator

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

NIH

collaborator

University of Minnesota

OTHER

collaborator

University of California, Los Angeles

OTHER

lead

Patricia I. Dickson, M.D.

INDIV