Pompe Disease (Late-Onset) Clinical Trial
Official title:
A Phase 4 Prospective Exploratory Muscle Biopsy, Biomarker, and Imaging Assessment Study in Patients With Late-Onset Pompe Disease Treated With Alglucosidase Alfa
This is an open-label, multicenter study of participants with late-onset Pompe disease naive
to treatment with enzyme replacement therapy (ERT). The primary objective of this study is
to evaluate glycogen clearance in muscle tissue samples collected pre and post alglucosidase
alfa treatment in participants with Late-Onset Pompe disease.
The secondary objectives are to characterize the disease burden in participants with
late-onset Pompe disease and explore imaging, histologic, and functional assessments in
these participants and to explore potential plasma or urine biomarkers relative to
late-onset Pompe disease and participant's response to treatment with alglucosidase alfa
(Myozyme®/Lumizyme®/GZ419829).
n/a
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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