Givlaari (givosiran sodium)

AHP Agents - ALAS1 mRNA Degradation Subcutaneous Vial (Ml)

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

Overview

Givosiran sodium is an aminolevulinate synthase 1-directed small interfering RNA.

Givosiran is a double-stranded small interfering RNA that causes degradation of aminolevulinate synthase 1 (ALAS1) messenger RNA (mRNA) in hepatocytes through RNA interference, reducing elevated levels of liver ALAS1 mRNA. This leads to reduced circulating levels of neurotoxic intermediates aminolevulinic acid (ALA) and porphobilinogen (PBG), factors associated with attacks, and other disease manifestations of acute hepatic porphyria.

Following subcutaneous administration, the median time to peak plasma concentrationis 3 hours (range, 0.5-8 hours) for givosiran and 7 hours (range, 1.5-12 hours) for the active metabolite, AS(N-1)3' givosiran. Givosiran and its active metabolite distribute primarily to the liver. The steady-state maximum plasma concentration (Cmax) andAUC for givosiran and the active metabolite increase proportionally up to a dosage of 2.5 mg/kg per month.

There is no accumulation of givosiran or the active metabolite following multiple dosing. Givosiran sodium is 90% bound to plasma proteins; plasma protein binding is concentration dependent and decreases with increasing givosiran concentrations (92% at 1 mcg/mL to 21% at 50 mcg/mL). Givosiran is metabolized by nucleases to oligonucleotides of shorter lengths.

Givosiran is not a substrate of cytochrome P450 (CYP) isoenzymes. The elimination half-life of both givosiran and the active metabolite is 6 hours. Givosiran is 5-14% excreted in the urine; 4-13% of the active metabolite is recovered in the urine.

There are no clinically meaningful differences in givosiran pharmacokinetics or pharmacodynamics based on sex or race/ethnicity.

USES: Givosiran is used to treat a certain inherited disorder (acute hepatic porphyria). This disorder causes a buildup of certain chemicals (porphyrins) in the body which can lead to liver and nerve problems. Givosiran works by reducing the amount of porphyrins in the body.

Generic name: givosiran sodium
Pronunciation: (GIV-oh-SIR-an)
Drug class: AHP Agents - ALAS1 mRNA Degradation
Therapeutic class: Hepatobiliary System Treatment Agents

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Givlaari:

  • Acute Hepatic Porphyria

Dosing

In patients with severe or clinically significant aminotransferase elevations who have dose interruption and subsequent improvement, reduce dosage to 1.25 mg/kg subcutaneously once monthly. In patients who resume dosing at 1.25 mg/kg once monthly without recurrence of severe or clinically significant aminotransferase elevations, the dosage may be increased to 2.5 mg/kg once monthly.

Drug interactions

There is no enhanced messaging for this drug.

Contraindications

*Known severe hypersensitivity to givosiran.

Adverse reactions

The most common adverse reactions reported in >=20% of patientsin clinical studies of givosiran include nausea and injection site reactions.

Precautions

No enhanced messaging available.

ICD codes

CodeTypeDescription
Acute hepatic porphyria
E80.21ICD10CMAcute intermittent (hepatic) porphyria
E80.29ICD10CMOther porphyria

ICD code information from First Databank (FDB).

Formulary status

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