Viltepso (viltolarsen)

Duchenne Muscular Dystrophy-Exon Skipping Antisense Oligonuc Intravenous Vial (Ml)

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

Overview

Viltolarsen is an antisense oligonucleotide of the phosphorodiamidate morpholino oligomer subclass.

Viltolarsen is an antisense oligonucleotide of the phosphorodiamidate morpholino oligomer subclass; the drug binds to exon 53 of dystrophin pre-mRNA. In patients with Duchenne muscular dystrophy (DMD), frameshift mutations in the dystrophin gene disrupt the translational reading frame, resulting in the production of a nonfunctional dystrophin protein. Lack of dystrophin results in degeneration and necrosis of muscle fibers, inflammation, and ultimately replacement of muscle by fibrotic and adipose tissue.

By targeting a region in exon 53, viltolarsen restores the mRNA reading frame, inducing production of de novo truncated dystrophin protein.

Following IV infusions of viltolarsen, peak plasma concentrations are reached at the end of the infusion. Viltolarsen plasma protein binding ranges from 39% to 40% and is not concentration dependent. Viltolarsen is not metabolized by hepatic enzymes and no metabolites are detected in plasma or urine.

The drug is mainly excreted unchanged in the urine with an elimination half-life of 2.5 hours.

USES: Viltolarsen is used to treat a certain inherited muscle disorder (Duchenne muscular dystrophy-DMD). This disorder is caused by a lack of a certain muscle protein (dystrophin). This medication can increase the amount of dystrophin in your body.

Generic name: viltolarsen
Pronunciation: (VIL-toe-LAR-sen)
Drug class: Duchenne Muscular Dystrophy-Exon Skipping Antisense Oligonuc
Therapeutic class: Locomotor System

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Viltepso:

  • Duchenne Muscular Dystrophy Due To Genetic Mutation Amenable To Exon 53 Skipping Therapy

Also known as: Dmd Amenable To Exon Skipping Therapy - Exon 53, Dmd Due To Genetic Mutation Amenable To Exon 53 Skipping, Duchenne Muscular Dystrophy Amenable To Exon 53 Skipping.

Dosing

No dosing information is available for this tab.

Drug interactions

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Contraindications

*None.

Adverse reactions

The most common adverse reactions (>=15%) reported with viltolarsen in clinical studies were upper respiratory tract infection, injection site reaction, cough, and pyrexia.

Precautions

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ICD codes

CodeTypeDescription
Duchenne muscular dystrophy due to genetic mutation amenable to exon 53 skipping therapy
G71.01ICD10CMDuchenne or becker muscular dystrophy

ICD code information from First Databank (FDB).

Formulary status

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