Evkeeza (evinacumab-dgnb)
Antihyperlipidemic - Angiopoietin-like 3 (ANGPTL3) Inhibitor Intravenous Vial (Ml)
Last reviewed · Source: First Databank (FDB) drug data
Overview
Evinacumab-dgnb, an angiopoietin-like protein 3 (ANGPTL3) inhibitor, is an antilipemic agent.
Evinacumab-dgnb, a human monoclonal antibody produced by recombinant DNA technology in Chinese hamster ovary cells, is an inhibitor of angiopoetin-like protein 3 (ANGPTL3), which is primarily expressed in the liver. ANGPTL3 helps to regulate lipid metabolism via inhibition of lipoprotein lipase (LPL) and endothelial lipase (EL), and when inhibited by evinacumab, leads to reductions in LDL-C, HDL-C, and triglycerides. Evinacumab reduction of LDL-C occurs upstream from LDL formation by promoting very low-density lipoprotein (VLDL) processing, independent from the presence of LDL receptor (LDLR).
By rescuing LPL and EL activities via ANGPTL3 inhibition, evinacumab lowers TG and HDL-C levels.
Based on a dosage of 15 mg/kg every 4 weeks, evinacumab-dgnb reaches steady state after the administration of 4 doses. Evinacumab exhibits nonlinear clearance. The median time for serum concentrations of evinacumab to decrease below the lower limit of quantitation is 19 weeks after the last dose.
Metabolism of evinacumab has not been fully characterized; however, as a monoclonal IgG4 antibody, evinacumab is expected to undergo degradation to small peptides and amino acids via catabolic pathways similar to endogenous IgG. Elimination of evinacumab occurs via parallel linear and non-linear pathways, and at high concentrations, is eliminated via a non-saturable proteolytic pathway. At lower concentrations, elimination is primarily mediated via ANGPTL3.
The elimination half-life of evinacumab is not constant and is a function of serum evinacumab concentrations. Evinacumab likely does not undergo renal excretion. Systemic exposure of evinacumab is not impacted by age (12-75 years), gender, body weight (42-152 kg), or race (Asian, Black or African-American, White, or Other).
USES: Evinacumab is used to treat a certain high cholesterol disorder (homozygous familial hypercholesterolemia-HoFH). It is used along with a proper diet and other LDL-lowering treatments (such as "statin" drugs, ezetimibe, LDL apheresis). Evinacumab belongs to a class of drugs known as monoclonal antibodies.
It works by blocking a certain protein that stops your body from properly breaking down cholesterol. This effect helps decrease "bad cholesterol" and fats (such as LDL, triglycerides). In addition to eating a proper diet (such as a low-cholesterol/low-fat diet), other lifestyle changes that may help this medication work better include exercising, losing weight if overweight, and stopping smoking.
Consult your doctor for more details.
Generic name: evinacumab-dgnb
Pronunciation: (E-vin-AK-ue-mab)
Drug class: Antihyperlipidemic - Angiopoietin-like 3 (ANGPTL3) Inhibitor
Therapeutic class: Cardiovascular Therapy Agents
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Evkeeza
Indications
The following indications are listed for Evkeeza:
- Homozygous Familial Hypercholesterolemia
Also known as: Familial Homozygous Hypercholesterolemia.
Dosing
No dosing information is available for this tab.
Evinacumab-dgnb is administered by IV infusion over 60 minutes through an IV line containing a sterile, in-line or add-on, 0.2-5 micron filter. The drug is available as a concentrate for injection that must be diluted prior to administration.
In patients with HoFH receiving lipoprotein apheresis, evinacumab may be administered without regard to timing of the procedure.
Store evinacumab concentrate for injection between 2-8degreesC in the original carton to protect from light. Do not freeze or shake.
Evinacumab concentrate for injection is preservative-free. Discard any unused portion left in the single-use vial after preparation.
If a dose of evinacumab is missed, the missed dose should be administered as soon as possible. Adjust the monthly infusion schedule thereafter based on the date of the last dose administered.
Do not mix other medications with evinacumab or administer other medications concomitantly via the same infusion line.
Slow, interrupt, or discontinue the infusion if the patient develops any signs of adverse reactions, including infusion or hypersensitivity reactions.
| Drug label | Dosing type | Instructions |
|---|---|---|
| Evkeeza 1,200 Mg/8 Ml Vial | Maintenance | Infuse 15 mg/kg over 60 minute(s) by intravenous route every 4 weeks. |
| Evkeeza 345 Mg/2.3 Ml Vial | Maintenance | Infuse 15 mg/kg over 60 minute(s) by intravenous route every 4 weeks. |
No dosing information is available for this tab.
Drug interactions
No formal drug interaction studies have been performed with evinacumab.
There are no contraindication interactions for this drug.
Severe Interaction: Action is required to reduce the risk of severe adverse interaction.
Igg Antibodies And Derivatives/Efgartigimod-Alfa
SEVERITY LEVEL: 2-Severe Interaction: Action is required to reduce the risk of severe adverse interaction.
MECHANISM OF ACTION: The neonatal Fc receptor (FcRn) prevents catabolism and mediates recycling of IgG and albumin, which leads to their long persistence in the body.(1,2) Efgartigimod-alfa binds to FcRn and may decrease systemic exposure of other ligands of FcRn, like immunoglobulins and IgG-based antibodies.(3)
CLINICAL EFFECTS: The effectiveness of medicines that bind to FcRn may be decreased.(3)
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: The manufacturer of efgartigimod-alfa states that efgartigimod-alfa should not be combined with long-term use of FcRn-binding medications. If the medication is essential for the patient, efgartigimod-alfa should be discontinued.(3)
DISCUSSION: Clinical drug interaction studies with efgartigimod-alfa have not been performed. Efgartigimod-alfa may decrease concentrations of compounds that bind to the human FcRn.(3)
Igg Antibodies And Derivatives/Nipocalimab-Aahu
SEVERITY LEVEL: 2-Severe Interaction: Action is required to reduce the risk of severe adverse interaction.
MECHANISM OF ACTION: The neonatal Fc receptor (FcRn) prevents catabolism and mediates recycling of IgG and albumin, which leads to their long persistence in the body.(1,2) Nipocalimab-aahu binds to FcRn and may decrease systemic exposure of other ligands of FcRn, like immunoglobulins and IgG-based antibodies.(3)
CLINICAL EFFECTS: The effectiveness of medicines that bind to FcRn may be decreased.(3)
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: The manufacturer of nipocalimab-aahu states that nipocalimab-aahu should not be combined with long-term use of FcRn-binding medications. If the medication is essential for the patient, nipocalimab-aahu should be discontinued.(3)
DISCUSSION: Clinical drug interaction studies with nipocalimab-aahu have not been performed. Nipocalimab-aahu may decrease concentrations of compounds that bind to the human FcRn.(3)
Moderate Interaction: Assess the risk to the patient and take action as needed.
Igg Antibodies And Derivatives/Rozanolixizumab-Noli
SEVERITY LEVEL: 3-Moderate Interaction: Assess the risk to the patient and take action as needed.
MECHANISM OF ACTION: The neonatal Fc receptor (FcRn) prevents catabolism and mediates recycling of IgG and albumin, which leads to their long persistence in the body.(1,2) Rozanolixizumab-noli binds to FcRn and may decrease systemic exposure of other ligands of FcRn, like immunoglobulins and IgG-based antibodies.(3)
CLINICAL EFFECTS: The effectiveness of medications that bind to FcRn may be decreased.(3)
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: The manufacturer of rozanolixizumab-noli states that concurrent use with medications that bind to the human neonatal Fc receptor (FcRn) should be closely monitored for reduced effectiveness of these medications. If long-term use of such medications is essential for the patient, consider discontinuing rozanolixizumab-noli and use alternative therapies.(3)
DISCUSSION: Clinical drug interaction studies with rozanolixizumab-noli have not been performed. Rozanolixizumab-noli may decrease concentrations of compounds that bind to the human FcRn.(3)
Contraindications
*History of serious hypersensitivity reactions to evinacumab or to any excipients.
There are no contraindication contraindications for this drug.
- Pregnancy
There are no moderate contraindications for this drug.
Adverse reactions
Adverse reactions reported in >=5% of patients receiving evinacumab-dgnb include nasopharyngitis, influenza-like illness, dizziness, rhinorrhea, fatigue, and nausea.
Infusion reactions occurred in 7% of patients receiving evinacumab, and more frequently with the drug than with placebo. Infusion reactions include infusion site pruritis, pyrexia, muscular weakness, nausea, and nasal congestion.
Less Frequent
- Anaphylaxis
- Hypersensitivity drug reaction
More Frequent
- Dizziness
- Flu-like symptoms
- Nausea
- Pharyngitis
- Rhinorrhea
Less Frequent
- Acute abdominal pain
- Constipation
- Fever
- General weakness
- Injection site sequelae
- Muscle weakness
- Nasal congestion
- Pain in extremities
- Upper respiratory infection
Precautions
No enhanced messaging available.
Safety and efficacy of evinacumab-dgnb as an adjunct to other LDL-C-lowering therapies for the treatment of HoFH have been established in pediatric patients >=1 year of age. Evidence from adequate and well-controlled studies in adults and additional pharmacokinetic, efficacy, and safety data in pediatric patients >=1 year of age support this use. The safety profile of evinacumab-dgnb in pediatric patients 1-11 years of age was similar to the safety profile in adults and pediatric patients >=12 years of age, with the additional adverse reaction of fatigue in pediatric patients aged 5-11 years of age.
Safety and efficacy of evinacumab have not been established in pediatric patients with HoFH who are <1 year of age.
Animal data indicate that evinacumab-dgnb may cause fetal harm if used during pregnancy. Human data are inadequate to determine the risk of fetal malformations, miscarriage, and adverse outcomes associated with use of evinacumab during pregnancy. Human immune globulin G (IgG) is known to cross the placenta; therefore, evinacumab, a human IgG4 antibody, has the potential to cross the placental barrier and be transmitted to the developing fetus. Animal studies indicate that evinacumab crosses the placental barrier. In animal studies, an increase in fetal malformations was observed when evinacumab was administered during organogenesis.
If a patient becomes pregnant while on evinacumab, providers should call 1-833-385-3392 to report exposure.
It is not known whether evinacumab is distributed into human or animal milk. However, maternal IgG is known to be present in human milk. The effects of the drug on the breastfed infant or on the production of milk are not known. The benefits of breastfeeding should be balanced with the potential for adverse effects from evinacumab exposure to the breastfed infant, along with the mother's clinical need for evinacumab.
The manufacturer makes no specific dosage recommendations for geriatric patients.
Insufficient numbers of patients >=65 years of age were included in clinical studies of evinacumab to determine whether there are differences in response compared to younger patients.
ICD codes
| Code | Type | Description |
|---|---|---|
| Homozygous familial hypercholesterolemia | ||
| E78.010 | ICD10CM | Homozygous familial hypercholesterolemia [hoFh] |
ICD code information from First Databank (FDB).
Formulary status
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Last reviewed · Source: First Databank (FDB) drug data
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