ISU Abxis Co., Ltd.
Quick facts
Marketed products
- Cerezyme® · Rare genetic disease / Lysosomal storage disorder
Cerezyme is an enzyme replacement therapy that provides the missing glucocerebrosidase enzyme to break down glucocerebroside in patients with Gaucher disease.
Phase 3 pipeline
- Fabagal® (Agalsidase beta) · Rare genetic disease / Lysosomal storage disorder
Agalsidase beta is a recombinant human enzyme that replaces deficient α-galactosidase A, breaking down accumulated globotriaosylceramide (Gb3) in cells.
Phase 1 pipeline
Competitive intelligence
For the full portfolio CI brief — phase mix, recent regulatory actions, upcoming PDUFA dates, patent timeline, class-overlap with competitors: