9
Participants
Start Date
June 30, 2009
Primary Completion Date
April 30, 2015
Study Completion Date
April 30, 2015
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.
University of Minnesota, Minneapolis
Los Angeles Biomedical Institute at Harbor-UCLA, Torrance
Children's Hospital & Research Center Oakland, Oakland
Collaborators (1)
The Ryan Foundation
OTHER
BioMarin Pharmaceutical
INDUSTRY
Rare Diseases Clinical Research Network
NETWORK
National Center for Advancing Translational Sciences (NCATS)
NIH
National Institute of Neurological Disorders and Stroke (NINDS)
NIH
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
NIH
University of Minnesota
OTHER
University of California, Los Angeles
OTHER
Patricia I. Dickson, M.D.
INDIV