Skip to content

Evinacumab

Published: July 26, 2026Updated: July 26, 2026

Evinacumab is a recombinant human monoclonal antibody that binds to and inhibits ANGPTL3 (angiopoietin-like protein 3), a liver-expressed protein that regulates lipid metabolism. It is primarily used as an adjunct therapy for homozygous familial hypercholesterolemia (HoFH) in patients who require additional lowering of LDL-C or other lipid parameters despite other treatments.

Quick summary

A monoclonal antibody that inhibits ANGPTL3 to lower cholesterol and triglycerides, used for homozygous familial hypercholesterolemia.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy

Key facts at a glance

ATC
C10AX17
RxNorm
2478335
Generic
Evinacumab
Class
atc-c10
Brands
Evkeeza
Availability
rx
Lactation
unknown
Routes
—
Forms
injection
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)IV infusion
Usual dose
15 mg/kg every 4 weeks
Maximum
consult physician
Frequency
once monthly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)IV infusion
Usual dose
15 mg/kg every 4 weeks
Maximum
consult physician
Frequency
once monthly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)IV infusion
Usual dose
15 mg/kg every 4 weeks
Maximum
consult physician
Frequency
once monthly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: No specific toxic dose established; doses up to 4500 mg have been administered in clinical trials without fatal outcomes
Chronic overdose: No cumulative toxicity data available for chronic overdose
Immediate actions
Discontinue infusion, monitor vital signs, provide supportive care, treat infusion reactions with standard medications
Antidote
No specific antidote exists(Supportive care is primary treatment; no antidote proven effective)
Poison Control: 1-800-222-1222

Special Populations

10 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks; discuss with healthcare provider

Monitor

regular fetal monitoring recommended

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

continue only if clearly needed; weigh benefits vs risks with cardiologist

Monitor

regular fetal monitoring including ultrasounds

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid near term if possible

Key Recommendations

discuss timing of last dose with healthcare provider; consider risks of continued use

Monitor

fetal monitoring and assessment of placental function

Use with caution and monitor for adverse effects.

?

lactation

breastfeeding
unknown
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

discontinue breastfeeding or avoid use; decision should be made weighing benefits and risks

Monitor

monitor infant for immune system effects

✓

geriatric

elderly 65 and older
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

use standard dosing; monitor cardiovascular status

Monitor

regular monitoring of lipid levels and cardiovascular function

✓

pediatric_age

adolescents 12 to 17
safe
FDA Category
C
Dose Adjustment

no dose adjustment

Key Recommendations

approved for patients 12 years and older with homozygous familial hypercholesterolemia

Monitor

regular lipid panel monitoring and liver function tests

✓

renal_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

no renal dose adjustment needed; monoclonal antibodies not renally cleared

Monitor

routine renal function monitoring

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

limited data in severe renal impairment; monitor closely

Monitor

enhanced renal function monitoring

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

no adjustment needed for mild hepatic impairment

Monitor

routine liver function monitoring

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

limited data in moderate to severe hepatic impairment; benefits vs risks must be assessed

Monitor

regular liver function tests and monitoring

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classFDA
2023

Drug class

Value:Monoclonal antibody (ANGPTL3 inhibitor)

Classification as a monoclonal antibody targeting ANGPTL3

regulatoryFDA
2023

FDA approval year

Value:2021

FDA approval date for Evkeeza

usageFDA
2023

Indication

Value:Adjunct treatment for homozygous familial hypercholesterolemia (HoFH)

Primary therapeutic indication

mechanismFDA
2023

Mechanism of action

Value:Inhibition of angiopoietin-like protein 3 (ANGPTL3)

Pharmacological mechanism of action

Evinacumab is indicated as an adjunct to other lipid-lowering therapies (such as statins, PCSK9 inhibitors, and LDL apheresis) for the treatment of adult and pediatric patients 12 years and older with homozygous familial hypercholesterolemia (HoFH), a rare genetic disorder causing severely elevated LDL cholesterol levels.

Evinacumab is a fully human IgG2 monoclonal antibody that binds to and inhibits ANGPTL3. By blocking ANGPTL3, it increases the activity of lipoprotein lipase and endothelial lipase, leading to reduced triglycerides and LDL cholesterol levels. This mechanism is independent of LDL receptor activity, making it effective even in patients with limited LDL receptor function.

Administered as an intravenous infusion every 4 weeks. Common side effects may include nasopharyngitis, influenza-like illness, dizziness, and back pain. It should be used with caution in patients with known hypersensitivity. Pregnancy and breastfeeding should be carefully considered, as effects on the fetus are not fully established.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

WellAlly may earn a referral fee from linked resources at no extra cost to you. Editorial content is never influenced by commercial relationships.

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed July 26, 2026. · Read our editorial policy