Alglucosidase alfa - Pharmacy benefit management

This medication was approved for use in patient’s ≥ 8 years old without cardiac hypertrophy suffering from late-onset Pompe disease.1 Pompe disease, also referred to as glycogen-storage disease type II or acid-maltase deficiency, is an autosomal recessive disease causing a deficiency in the lysosomal enzyme acid alpha-glucosidase (GAA). ................
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