Pombiliti (cipaglucosidase alfa-atga)

Metabolic Disease Enzyme Replacement, Pompe Disease Intravenous Vial (Ea)

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

Overview

Cipaglucosidase alfa-atga is a hydrolytic lysosomal glycogen-specific enzyme.

Pompe disease is an inherited disorder of glycogen metabolism caused by a deficiency of lysosomal acid alpha-glucosidase (GAA) that degrades glycogen to glucose in the lysosome. GAA deficiency results in intra-lysosomal accumulation of glycogen in various tissues. Cipaglucosidase alfa-atga is a hydrolytic lysosomal glycogen-specific recombinant human alpha-glucosidase enzyme that provides an exogenous source of GAA.

The bis-mannose-6-phosphate on cipaglucosidase alfa-atga mediates binding to mannose-6-phosphate receptors on the cell surface with high affinity. After binding, it is internalized and transported into lysosomes where it undergoes proteolytic cleavage and N-glycans trimming, which are both required to yield the most mature and active form of GAA. Cipaglucosidase alfa-atga then exerts enzymatic activity in cleaving glycogen.

Cipaglucosidase alfa-atga must be given in combination with miglustat; miglustat binds with, stabilizes, and reduces inactivation of cipaglucosidase alfa-atga in the blood after infusion.

When administered in combination with miglustat, the mean half-life of cipaglucosidase alfa-atga is 2.1 hours. Plasma protein binding and the metabolic pathway of cipaglucosidase alfa-atga have not been characterized. Metabolism by cytochrome P-450 enzymes or secretion into bile is not a significant contributor to elimination; cipaglucosidase alfa-atga is expected to be metabolized into small peptides and amino acid via catabolic pathways.

Intact cipaglucosidase alfa-atga is unlikely to be filtered by the kidney or excreted in the urine. Age (18 to 74 years) and sex did not have clinically meaningful effects on the pharmacokinetics of cipaglucosidase alfa-atga.

USES: Cipaglucosidase alfa is used in combination with another medication (miglustat) to treat a certain inherited condition (Pompe disease). It works by breaking down a certain substance (glycogen) that builds up in the body due to this condition. Decreasing glycogen in the body can help improve symptoms of Pompe disease such as muscle weakness, heart problems, and breathing problems.

This medication must be used with miglustat because it helps cipaglucosidase alfa stay active in the blood which helps it work better.

Generic name: cipaglucosidase alfa-atga
Pronunciation: (SIP-a-gloo-KOE-si-dase Al-fa)
Drug class: Metabolic Disease Enzyme Replacement, Pompe Disease
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 Pombiliti:

  • Lysosomal Alpha-1,4-Glucosidase Deficiency

Also known as: Acid Maltase Deficiency, Glycogen Storage Disease Type 2, Glycogen Storage Disease Type Ii, Glycogenosis Type Ii, Pompe's Disease.

Dosing

No dosing information is available for this tab.

Drug interactions

No formal drug interaction studies have been conducted to date; cipaglucosidase alfa-atga is unlikely to be involved in cytochrome P-450 (CYP) or transporter-mediated drug interactions.

Contraindications

*Pregnancy.

Adverse reactions

The most common adverse effects of cipaglucosidase alfa-atga (>=5% of patients) reported in clinical studies include headache, diarrhea, fatigue, nausea, abdominal pain, and pyrexia.

Precautions

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ICD codes

CodeTypeDescription
Lysosomal alpha-1,4-glucosidase deficiency
E74.02ICD10CMPompe disease

ICD code information from First Databank (FDB).

Formulary status

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