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Brodalumab

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

Brodalumab is a monoclonal antibody that targets the IL-17 receptor A, blocking inflammatory signals involved in autoimmune conditions. It is primarily used to treat moderate to severe plaque psoriasis in patients who are candidates for systemic therapy or phototherapy.

Quick summary

An IL-17 receptor antagonist used to treat moderate to severe plaque psoriasis by blocking inflammatory cytokine signaling.

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

This medication carries a boxed (black box) warning — the strongest type of FDA warning. Review the full prescribing information before use.

Key facts at a glance

ATC
L04AC12
RxNorm
1872251
Generic
Brodalumab
Class
atc-l04
Brands
Siliq
Availability
rx
Lactation
unknown
Routes
—
Forms
prefilled syringe
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)subcutaneous injection
Usual dose
210mg
Maximum
consult physician
Frequency
every 2 weeks (after loading doses at weeks 0, 1, and 2)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (not approved)N/A
Usual dose
not approved for pediatric use
Maximum
consult physician
Frequency
N/A
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)subcutaneous injection
Usual dose
210mg
Maximum
consult physician
Frequency
every 2 weeks (after loading doses at weeks 0, 1, and 2)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose significantly above therapeutic dose that may cause serious toxicity
Chronic overdose: repeated dosing above recommended regimen leading to increased risk of infections and immune-related adverse events
Immediate actions
monitor vital signs, supportive care, discontinue medication, evaluate for infections
Antidote
no specific antidote available(supportive care is primary treatment, no specific reversal agent)
Poison Control: 1-800-222-1222

Special Populations

9 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks; consider discontinuation prior to conception

Monitor

regular fetal monitoring and ultrasound assessments

Use of this medication in this population requires careful consideration of risks and benefits.

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid

Key Recommendations

monoclonal antibodies may cross placenta; avoid use in third trimester

Monitor

close fetal monitoring

Use of this medication in this population requires careful consideration of risks and benefits.

?

lactation

breastfeeding
unknown
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

discontinue breastfeeding or discontinue drug; decision should be made based on benefit-risk assessment

Monitor

monitor infant for infections

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

use with caution; no dose adjustment required but monitor for infections

Monitor

regular assessment of infection symptoms

Use with caution and monitor for adverse effects.

✗

pediatric_age

peds under 18
unsafe
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

not approved for use in patients under 18 years of age; safety and efficacy not established

Monitor

not applicable

Use of this medication in this population requires careful consideration of risks and benefits.

✓

renal_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

no dose adjustment required; brodalumab is a monoclonal antibody not renally cleared

Monitor

standard monitoring

✓

renal_impairment

severe
safe
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

no dose adjustment required based on pharmacokinetic data

Monitor

standard monitoring

✓

hepatic_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no adjustment

Key Recommendations

no dose adjustment required; monoclonal antibodies metabolized by proteolysis

Monitor

standard monitoring

⚠

hepatic_impairment

severe
caution
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

use with caution; limited data in severe hepatic impairment

Monitor

monitor liver function tests

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2017

FDA approval for Brodalumab (Siliq) for treatment of moderate-to-severe plaque psoriasis

drug_classFDA
2023

Drug class

Value:IL-17 receptor antagonist (Biologic)

Monoclonal antibody that binds to the IL-17 receptor

usageFDA
2023

Approved indications

Value:Moderate-to-severe plaque psoriasis

Therapeutic indication for Brodalumab

administrationFDA
2023

Route of administration

Value:Subcutaneous injection

Method of drug administration

Brodalumab is approved for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy or phototherapy. It may also be considered for psoriatic arthritis in certain cases.

Brodalumab is a human monoclonal IgG2 antibody that selectively binds to the IL-17 receptor A (IL-17RA) on cell surfaces, preventing interaction with pro-inflammatory cytokines including IL-17A, IL-17F, IL-17C, IL-17A/F heterodimer, and IL-25. By blocking these cytokine-receptor interactions, it inhibits downstream inflammatory signaling pathways that contribute to psoriasis pathogenesis.

Brodalumab is administered via subcutaneous injection. Patients should be monitored for infections, as IL-17 inhibition may increase susceptibility to fungal and bacterial infections. Suicidal ideation and behavior have been observed in some patients during clinical trials; patients should be assessed for depression and suicidal thoughts before and during treatment. Brodalumab should not be used in patients with active infections.

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

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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