Agalsidase Beta
A recombinant enzyme used to treat Fabry disease by replacing the deficient alpha-galactosidase A enzyme responsible for breaking down fatty deposits in the body. Regular infusions help reduce the buildup of globotriaosylceramide in kidneys, heart, and other organs, slowing the progression of kidney damage and other complications.
Area Terapeutik
Mekanisme Kerja
As a recombinant protein, it replicates the function of the naturally occurring human protein, supplementing or replacing deficient endogenous production to restore normal physiological activity.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
As a recombinant protein, it replicates the function of the naturally occurring human protein, supplementing or replacing deficient endogenous production to restore normal physiological activity.
HBD / HBA
- / -
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Pertanyaan yang Sering Diajukan
A recombinant enzyme used to treat Fabry disease by replacing the deficient alpha-galactosidase A enzyme responsible for breaking down fatty deposits in the body. Regular infusions help reduce the buildup of globotriaosylceramide in kidneys, heart, and other organs, slowing the progression of kidney damage and other complications.
As a recombinant protein, it replicates the function of the naturally occurring human protein, supplementing or replacing deficient endogenous production to restore normal physiological activity.
Yes, Agalsidase Beta is an approved drug. It has reached clinical phase 4. It is classified as a Enzyme.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2108888. Open-access bioactivity database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-02-27.
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