Aldurazyme (laronidase)

Metabolic Disease Enzyme Replacement - Mucopolysaccharidosis Intravenous Vial (Ml)

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Laronidase is a biosynthetic (recombinant DNA origin) replacement form of l-iduronidase, a lysosomal enzyme that catalyzes the hydrolysis of terminal alpha-l-iduronic acid residues of dermatan sulfate and heparan sulfate.

Laronidase is a biosynthetic (recombinant DNA origin) form of l-iduronidase (alpha-l-iduronidase), a lysosomal enzyme that catalyzes the hydrolysis of terminal alpha-l-iduronic acid residues of the glycosaminoglycan substrates dermatan sulfate and heparan sulfate. Laronidase is prepared from cultures of genetically modified mammalian (Chinese hamster ovary) cells using recombinant DNA technology. In patients with MPS I, laronidase provides an exogenous source of l-iduronidase for uptake into lysosomes and catabolism of glycosaminoglycans.

The mean elimination half-life of laronidase is 1.5 to 3.6 hours.

USES: Laronidase is used to treat a certain rare genetic problem (mucopolysaccharidosis-MPS I). It works by replacing a certain natural substance (lysosomal enzyme) that is missing in people with this genetic problem. This medication improves lung function and how far you can walk.

Laronidase is not a cure and treatment must be continued for life.

Generic name: laronidase
Pronunciation: (lar-ON-i-dase)
Drug class: Metabolic Disease Enzyme Replacement - Mucopolysaccharidosis
Therapeutic class: Metabolic Disease Enzyme Replacement Agents

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Aldurazyme:

  • Mucopolysaccharidosis Type I

Also known as: Alpha-L-Iduronidase Deficiency, Mps Type I.

Dosing

Dosage of laronidase is expressed in mg. The specific activity of laronidase is 172 units/mg.

Drug interactions

No formal drug interaction studies have been performed.

Contraindications

*None.

Adverse reactions

The most common adverse effects reported in >=10% of patients >=6 months of age include infusion reactions (e.g., pyrexia, chills, increased blood pressure, tachycardia, and decreased oxygen saturation).

The most common adverse effects reported in >=10% of patients >=6 years of age include rash, upper respiratory tract infection, injection site reaction, hyperreflexia, paresthesia, flushing, and poor venous access.

Precautions

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ICD codes

CodeTypeDescription
Mucopolysaccharidosis type I
E76.0ICD10CMMucopolysaccharidosis, type I
E76.01ICD10CMHurler's syndrome
E76.02ICD10CMHurler-scheie syndrome
E76.03ICD10CMScheie's syndrome

ICD code information from First Databank (FDB).

Formulary status

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Last reviewed · Source: First Databank (FDB) drug data