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Hepatology / Orphan drugs / Alglucosidase alfa / Clinical trial / Alpha-glucosidase / Lysosomal storage disease / Medicine / Health / Glycogen storage disease type II


Document Date: 2008-05-08 13:26:26

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Company

Genzyme Canada Inc. / /

Currency

USD / /

MedicalCondition

acid α-glucosidase deficiency / onset Pompe disease / cardiomyopathy / disease / lysosomal storage diseases / infantileonset Pompe disease / hypersensitivity / rare disease / infantile-onset Pompe disease / anaphylaxis / Pompe disease / /

MedicalTreatment

enzyme replacement therapy / intravenous infusion / /

Organization

Canadian Expert Drug Advisory Committee / /

Product

Myozyme / /

PublishedMedium

the Common Drug Review / /

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