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donidalorsen

Brand Name : Dawnzera

Synonyms : donidalorsen

Class : Kallikrein Inhibitors


ADULT DOSING

Dosage Forms & Strengths

SC solution, injection

single-dose autoinjector

0.8 ml/80 mg

Hereditary Angioedema (HAE)

Indicated for the prevention of hereditary angioedema (HAE) attacks

The suggested dose is 80 mg subcutaneously every four weeks

Administration every eight weeks may be considered

hereditary angioedema 

Indicated for the prevention of hereditary angioedema (HAE) attacks The suggested dose is 80 mg subcutaneously every four weeks Administration every eight weeks may be considered

ADULT DOSING

Dosage Forms & Strengths

SC solution, injection

single-dose autoinjector

0.8 ml/80 mg

Hereditary Angioedema (HAE)

Indicated for the prevention of hereditary angioedema (HAE) attacks

The suggested dose is 80 mg subcutaneously every four weeks

Administration every eight weeks may be considered

hereditary angioedema 

Indicated for the prevention of hereditary angioedema (HAE) attacks The suggested dose is 80 mg subcutaneously every four weeks Administration every eight weeks may be considered

DRUG INTERACTION

donidalorsen

&

Known drug interactions

No interactions found.

No interactions found.

No interactions found.

No interactions found.

Frequency Not Defined

Decreased platelet count

Hypersensitivity reactions

Anaphylaxis

Generalized rash

Dyspnea

Chest pain

Peri-oral swelling

Increased liver function tests

1-10%

Abdominal discomfort (7%)

Urinary tract infection (9%)

Upper respiratory tract infection (9%)

>10%

Injection site reactions (24%)

Action

A prekallikrein (PKK)–targeted antisense oligonucleotide (ASO) is chemically linked to a ligand containing three N-acetylgalactosamine (GalNAc) units, which enhances uptake of the ASO by hepatocytes.

Once inside the cell, the conjugate binds to PKK mRNA and triggers ribonuclease H1 (RNase H1)–mediated cleavage, leading to decreased synthesis of PKK protein.

Since PKK is a key activator of inflammatory pathways, its reduction helps limit the mediators responsible for acute episodes of hereditary angioedema.

Black Box Warning

None

Contraindication/Caution:

Contraindication:

Hypersensitivity reaction

Caution:

Hypersensitivity

Pregnancy Warnings:

Pregnancy category: N/A

Lactation: Excretion in human breastmilk is unknown

Pregnancy categories:

Category A: Satisfactory and well-controlled studies show no evidence of risk to the fetus in the first trimester or in the later trimester.

Category B: No evidence of risk to fetus found in animal reproduction studies and there are not enough studies on pregnant women.

Category C: Adverse effects on the fetus found with evidence in animal reproduction studies and no adequate evidence for an effect in humans, care must be taken for potential risks in pregnant women.

Category D: There is adequate data available with sufficient evidence of human fetal risk from various platforms, but despite potential risks may be used only in emergency cases for potential benefits.

Category X: Drugs listed in this category clearly outweigh risks over benefits. These category drugs should be prohibited for pregnant women.

Category N: There is no data available for the drug under this category.

Pharmacology:

A prekallikrein (PKK)–targeted antisense oligonucleotide (ASO) is chemically linked to a ligand containing three N-acetylgalactosamine (GalNAc) units, which enhances uptake of the ASO by hepatocytes.

Once inside the cell, the conjugate binds to PKK mRNA and triggers ribonuclease H1 (RNase H1)–mediated cleavage, leading to decreased synthesis of PKK protein.

Since PKK is a key activator of inflammatory pathways, its reduction helps limit the mediators responsible for acute episodes of hereditary angioedema.

Pharmacokinetics:

Absorption

The drug is absorbed with a peak plasma time of approximately 2 hours (range 0.25-8 hours). The peak plasma concentration is about 417 ng/mL with every 4-week dosing and 416 ng/mL with every 8-week dosing.

Distribution

The drug is highly protein bound (>98%). Its volume of distribution is 69.8 L in the central compartment and 1840 L in the peripheral compartment.

Metabolism

The drug is expected to be metabolized by endo- and exonucleases in the liver into short oligonucleotide fragments of varying sizes.

Elimination and excretion

Its elimination is characterized by a biphasic half-life, with an initial phase of approximately 5 hours reflecting tissue distribution and a terminal phase of about 1 month. Less than 1% of the administered dose is excreted in the urine.

Administration:

Subcutaneous injections should be given in the abdomen or upper thigh. A caregiver or healthcare professional may alternatively administer the injection in the back or upper arm. If a dose is missed, it should be taken as soon as possible, after which the treatment schedule should be continued based on the timing of the most recent dose.

Patient information leaflet

Generic Name: donidalorsen

Why do we use donidalorsen ?

Donidalorsen is a novel, RNA-targeted preventative therapy for hereditary angioedema.

Donidalorsen is approved for prophylaxis to prevent attacks of hereditary angioedema (HAE) in adults and adolescents aged 12 years and older.

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