A Phase II/ III multicenter, open-label, single-group, designed to evaluate the efficacy and safety of study drug for the treatment of the MPS II.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
28
IV infusion, 2.0 mg/kg/week
Fukui Clinical site
Fukui, Japan
Fukuoka Clinical site 2
Fukuoka, Japan
Fukuoka Clinical site
Change From Baseline in Heparan Sulfate Levels in Cerebrospinal Fluid
Time frame: Baseline to 52 weeks
Change From Baseline in Serum Heparan Sulfate Levels.
Time frame: Baseline, 24-26 weeks, 50-52 weeks
Change From Baseline in Serum Dermatan Sulfate Levels.
Time frame: Baseline, 24-26 weeks, 50-52 weeks
Change From Baseline in Urinary Heparan Sulfate Levels.
Time frame: Baseline, 25 weeks, 52 weeks
Change From Baseline in Urinary Dermatan Sulfate Levels.
Time frame: Baseline, 25 weeks, 52 weeks
Change From Baseline in Liver Volumes.
Time frame: Baseline, 25 weeks, 52 weeks
Change From Baseline in Spleen Volumes.
Time frame: Baseline, 25 weeks, 52 weeks
Change From Baseline in Cardiac Function.
Time frame: Baseline, 25 weeks, 52 weeks
Change From Baseline in 6-minute Walk Test Distance.
Item 9 will be administrated only in patients judged by the investigator or subinvestigator to be possible to perform the 6-minutes walk test
Time frame: Baseline, 25 weeks, 52 weeks
Change From Baseline in Joint Range of Motion.
Time frame: Baseline, 25 weeks, 52 weeks
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Fukuoka, Japan
Gifu Clinical site
Gifu, Japan
Hokkaido Clinical site
Hokkaido, Japan
Kanagawa Clinical site
Kanagawa, Japan
Kumamoto Clinical site
Kumamoto, Japan
Okayama Clinical site
Okayama, Japan
Okayama Clinical site 2
Okayama, Japan
Okinawa Clinical site
Okinawa, Japan
...and 9 more locations
Change From Baseline in Heparan Sulfate Levels in Cerebrospinal Fluid.
Time frame: Baseline to 25 weeks
Change From Baseline in Dermatan Sulfate Levels in Cerebrospinal Fluid.
Time frame: Baseline, 25 weeks, 52 weeks
Change from Baseline in Neurocognitive Testing (Kyoto Scale of Psychological Development 2001)
Time frame: 25, 52 weeks
Change from Baseline in Adaptive Behavioral Testing ( Vineland Adaptive Behavior Scales Second Edition. )
Time frame: 25, 52 weeks
Drug concentration in Cerebrospinal Fluid.
\*Drug concentration in Cerebrospinal Fluid at 52 Weeks is applicable only for subjects to be enrolled in extension study .
Time frame: 25, 52*weeks