A Phase I/ II, open-label study, designed to evaluate the safety and explore efficacy of the study drug in development for the treatment of MPS IIIB patients.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
IV infusion
Hiroshima University Hospital
Hiroshima, Japan
RECRUITINGUniversity of the Ryukyus Hospital
Okinawa, Japan
RECRUITINGNational Center for Child Health and Development
Tokyo, Japan
RECRUITINGTo establish the safety and tolerability of JR-446 in MPSIIIB patients
Time frame: up to 4 years (multiple visits)
To determine the pharmacodynamic effects of JR-446 in MPSIIIB patients
Time frame: up to 4 years (multiple visits)
To assess PK profile of JR-446 in MPSIIIB patients
Time frame: up to 4 years (multiple visits)
To explore the potential efficacy of JR-446 in the treatment of patients with MPS IIIB
Time frame: up to 4 years (multiple visits)
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