This is a single-center, open-label, multiple-dose study of the efficacy and long-term safety of Lamazym for the treatment of patients with alpha-mannosidosis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
10
ERT, infusion weekly
Department of Clinical Genetics, Juliane Marie Centre, Copenhagen University Hospital, Blegdamsvej 9
Copenhagen, Denmark
Reduction of Oligosaccharides in urine
Efficacy endpoint evaluation as change from baseline
Time frame: 3 months (interim evaluation) + 6 months
Reduction of Oligosaccharides in serum
Efficacy endpoint evaluation as change from baseline
Time frame: 3 months (interim evaluation) + 6 months
Reduction of Oligosaccharides in CSF
Efficacy endpoint evaluation as change from baseline
Time frame: 3 months (interim evaluation) + 6 months
The distance walked in 6 minutes
Efficacy endpoint evaluation as change from baseline
Time frame: 3 months (interim evaluation) + 6 months
The number of steps climbed in 3 minutes
Efficacy endpoint evaluation as change from baseline
Time frame: 3 months (interim evaluation) + 6 months
Pulmonary Function
Efficacy endpoint evaluation as change from baseline
Time frame: 3 months (interim evaluation) + 6 months
Adverse events
Safety endpoint assessed weekly throughout the trial
Time frame: 1 week
Development of clinically significant changes in vital signs and change in physical examination
Safety endpoint assessed weekly throughout the trial
Time frame: 1 week
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Development of clinically significant changes in the clinical laboratory parameters (hematology, biochemistry and urinalysis)
Safety endpoint assessed every 4th week throughout the trial
Time frame: 4 weeks
Development of rhLAMAN antibodies and neutralizing/inhibitory antibodies
Safety endpoint assessed every other week throughout the trial
Time frame: 2 weeks