A Phase I/ II, open-label, randomized, 2-arm study, designed to evaluate the safety and explore efficacy of the study drug in development for the treatment of MPS IIIA patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Universitätsklinikum Hamburg-Eppendorf
Hamburg, Germany
To evaluate the tolerability of JR-441 in MPSIIIA patients
Adverse events will be reported and graded, laboratory tests will be conducted and vital signs will be monitored
Time frame: up to 5 years (multiple visits)
To assess the safety of JR-441 in MPSIII-A patients
Number and severity of infusion-associated reactions, including anaphylaxis
Time frame: up to 5 years (multiple visits)
Plasma drug concentration
Time frame: up to 5 years (multiple visits)
Plasma PK parameters
Time frame: up to 5 years (multiple visits)
Change from baseline in heparan sulfate levels in cerebrospinal fluid (CSF), serum and urine
Time frame: up to 5 years (multiple visits)
Change from baseline in cognitive function
Bayley Scales of Infant and Toddler Development, Third Edition (BSID-III) and/or Kaufman Assessment Battery for Children, Second Edition (KABC-II)
Time frame: up to 5 years (multiple visits)
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