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Obiltoxaximab

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

Obiltoxaximab is a monoclonal antibody medication designed to treat and prevent anthrax, a serious infection caused by Bacillus anthracis bacteria. It works by binding to the protective antigen component of the anthrax toxin, preventing the toxin from entering and damaging human cells. This medication is used in both adult and pediatric patients for treatment of anthrax disease (in combination with other antibacterial drugs) and for post-exposure prophylaxis when standard antibiotics are not appropriate.

Quick summary

Obiltoxaximab is a monoclonal antibody that treats and prevents anthrax by neutralizing the anthrax toxin.

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
J06BC04
RxNorm
1746906
Generic
Obiltoxaximab
Class
atc-j06
Brands
Anthim
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)intravenous infusion
Usual dose
7mg/kg as single infusion
Maximum
consult physician
Frequency
single dose (one-time)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)intravenous infusion
Usual dose
7mg/kg as single infusion
Maximum
consult physician
Frequency
single dose (one-time)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)intravenous infusion
Usual dose
7mg/kg as single infusion
Maximum
consult physician
Frequency
single dose (one-time)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose exceeding 16 mg/kg (maximum 800 mg) may cause serious toxicity including severe hypersensitivity reactions and immune complex formation
Chronic overdose: Limited data available; cumulative dosing not recommended as Obiltoxaximab is typically administered as single dose; repeated dosing may increase risk of immunogenicity and hypersensitivity reactions
Immediate actions
Discontinue infusion immediately, maintain airway and adequate circulation, administer intravenous fluids and vasopressors if needed, provide supplemental oxygen, monitor vital signs continuously
Antidote
No specific antidote exists; treatment is supportive and symptomatic(Supportive care is the primary intervention; early recognition and discontinuation of infusion critical for favorable outcome)
Poison Control: 1-800-222-1222

Special Populations

10 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks; treat only if exposed to anthrax or suspected exposure

Monitor

regular fetal monitoring recommended

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

✗

pregnancy

second trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring recommended

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring recommended

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

?

lactation

breastfeeding
unknown
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

discontinue breastfeeding or pump and discard milk during treatment; decision should be made considering importance of drug to mother

Monitor

monitor infant for adverse effects

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

use with caution; no dose adjustment required based on pharmacokinetics; consider comorbidities and organ function

Monitor

monitor for infusion-related reactions and cardiovascular events

Use with caution and monitor for adverse effects.

?

pediatric_age

children
unknown
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

safety and efficacy not established in pediatric patients; use only if benefits outweigh risks in emergency situations

Monitor

monitor closely for infusion-related reactions

✓

renal_impairment

mild to moderate
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

no dose adjustment needed for mild to moderate renal impairment; monitor closely for infusion reactions

Monitor

standard monitoring for infusion-related reactions

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

use with caution; no specific dose adjustment recommended; monitor closely for adverse effects

Monitor

monitor closely for infusion-related reactions

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild to moderate
caution
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

use with caution; no specific dose adjustment recommended; limited data available

Monitor

monitor liver function tests and for infusion-related reactions

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

severe
caution
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

use with caution; no specific dose adjustment recommended; limited clinical data available

Monitor

monitor closely for infusion-related reactions and liver function

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2016

Initial FDA approval date for Obiltoxaximab (Anthim)

drug_classFDA
2023

Drug class

Value:Monoclonal antibody

Therapeutic monoclonal antibody class

usageFDA
2023

Indication

Value:Treatment and prevention of inhalational anthrax

Primary therapeutic indication

mechanismFDA
2023

Mechanism of action

Value:Neutralizes protective antigen (PA) of Bacillus anthracis

Pharmacological mechanism

Treatment of inhalational, cutaneous, or gastrointestinal anthrax in adult and pediatric patients (used in combination with appropriate antibacterial drugs); prophylaxis of anthrax when alternative therapies are not suitable or available.

Obiltoxaximab is a monoclonal antibody that specifically binds to the protective antigen (PA) of Bacillus anthracis, blocking the PA from interacting with cellular receptors and preventing the anthrax toxin from entering and damaging host cells.

Administered as an intravenous infusion; should be used with appropriate antibacterial drugs for treatment of anthrax disease; monitor for infusion-related reactions; included in the Strategic National Stockpile for biodefense preparedness.

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