The objective of this study is to determine the safety and efficacy of once weekly dosing of idursulfase-beta 0.5mg/kg administered by intravenous(IV) infusion for Hunter syndrome patients \< 6 years old.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
6
once weekly, 0.5mg/kg IV infusion
Samsug Medical Center
Seoul, South Korea
Incidence of adverse events
Time frame: One year
change of anti-idursulfase-beta antibody status
Time frame: baseline and one year
Percent Change of Urine GAG
Time frame: baseline to 53 weeks
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