15
Participants
Start Date
October 31, 2011
Primary Completion Date
February 29, 2016
Study Completion Date
February 29, 2016
BMN 110
Patients will receive intravenous (IV) infusions of study drug at a dose of 2.0 mg/kg/wk over a period of approximately 4 hours every week for up to 208 weeks.
Oakland
Manhasset
Monza
Taipei
Central Manchester
Lead Sponsor
BioMarin Pharmaceutical
INDUSTRY