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Mirikizumab

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

Mirikizumab is a monoclonal antibody medication used to treat inflammatory conditions by targeting the IL-23 pathway. It works by binding to the p19 subunit of IL-23, blocking its interaction with receptors and reducing inflammatory responses. This medication is primarily used for autoimmune disorders affecting the skin and gastrointestinal tract.

Quick summary

Mirikizumab is an immunosuppressant monoclonal antibody that targets IL-23 to treat inflammatory conditions like psoriasis and inflammatory bowel disease.

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

Key facts at a glance

ATC
L04AC24
RxNorm
2668384
Generic
Mirikizumab
Class
atc-l04
Brands
Omvoh
Availability
rx
Lactation
unknown
Routes
—
Forms
prefilled syringe, 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)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: No specific toxic single dose established for this monoclonal antibody biologic; overdosing is unlikely due to administration via healthcare-supervised IV infusion
Chronic overdose: cumulative toxicity information not established; long half-life of approximately 9 days may lead to prolonged exposure
Immediate actions
discontinue infusion, monitor vital signs, supportive care, consider corticosteroids for severe reactions
Antidote
no_specific_antidote(supportive care is primary management; no specific antidote exists for monoclonal antibody overdose)
Poison Control: 1-800-222-1222

Special Populations

6 groups
⚠

pregnancy

all trimesters
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits outweigh potential risks to fetus; discontinue if pregnancy occurs unless clearly needed

Monitor

regular prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

consider continuing if needed for maternal condition; weigh benefits against potential infant exposure

Monitor

monitor infant for infections

Use with caution and monitor for adverse effects.

✓

geriatric

elderly 65 and older
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

no dosage adjustment needed based on age; monitor for infections

Monitor

standard clinical monitoring

?

pediatric_age

pediatric under 18
unknown
FDA Category
N
Dose Adjustment

not established

Key Recommendations

not approved for use in pediatric patients; safety and efficacy not established

Monitor

not applicable

✓

renal_impairment

severe renal impairment
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

no dosage adjustment needed; monoclonal antibodies not renally cleared

Monitor

standard clinical monitoring

✓

hepatic_impairment

mild to moderate hepatic impairment
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

no dosage adjustment needed; monoclonal antibodies metabolized via proteolytic degradation

Monitor

standard clinical monitoring

Statistics and clinical data

prescribingFDA
2024

FDA approval year

Value:2023

First FDA approval for ulcerative colitis

drug_classFDA
2024

Drug class

Value:IL-23 inhibitor (monoclonal antibody)

Biologic immunotherapy targeting interleukin-23

usageFDA
2024

Common uses

Value:Ulcerative colitis, Crohn's disease

Approved therapeutic indications

mechanismFDA
2024

Mechanism of action

Value:Binds to p19 subunit of IL-23, blocking downstream inflammatory signaling

Pharmacodynamic mechanism

Mirikizumab is used to treat moderate to severe plaque psoriasis in adults who are candidates for systemic therapy, as well as moderately to severely active ulcerative colitis. It is administered as a subcutaneous injection.

Mirikizumab is a humanized IgG4 monoclonal antibody that selectively binds to the p19 subunit of the cytokine IL-23. By blocking IL-23 from binding to its receptor, it inhibits the downstream inflammatory signaling that drives the differentiation, expansion, and survival of inflammatory cells involved in mucosal inflammation.

As an immunosuppressant, mirikizumab may increase the risk of infections, including serious infections. It is contraindicated in patients with known hypersensitivity to the active substance or any excipients. Patients should be monitored for signs of infection during treatment and for a period after discontinuation.

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