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Panitumumab

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

Panitumumab is a fully human monoclonal antibody that targets the Epidermal Growth Factor Receptor (EGFR). It is primarily used to treat metastatic colorectal cancer with wild-type RAS tumors. The medication works by blocking EGFR signaling, thereby inhibiting tumor cell proliferation and survival.

Quick summary

Panitumumab is an EGFR-targeting monoclonal antibody used to treat metastatic colorectal cancer with wild-type RAS.

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
L01FE02
RxNorm
263034
Generic
Panitumumab
Class
atc-l01
Brands
Vectibix
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)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: Doses exceeding recommended 6mg/kg may cause severe skin toxicity and electrolyte abnormalities
Chronic overdose: Prolonged treatment with excessive cumulative exposure may lead to severe dermatologic toxicity and hypomagnesemia
Immediate actions
Discontinue infusion, monitor vital signs, provide supportive care, correct electrolyte imbalances
Antidote
No specific antidote available(Supportive care is mainstay of treatment)
Poison Control: 1-800-222-1222

Special Populations

8 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks to the fetus

Monitor

regular fetal monitoring and ultrasound assessments

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

discontinue therapy if pregnancy occurs and consider risks versus benefits

Monitor

regular fetal monitoring

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 near delivery due to potential effects on newborn

Monitor

monitor neonate for adverse effects

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

✗

lactation

breastfeeding
unsafe
FDA Category
N
Dose Adjustment

not applicable

Key Recommendations

do not breastfeed during treatment and for at least 2 months after last dose

Monitor

not applicable

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

no specific dose adjustment required

Key Recommendations

use with caution and monitor for adverse reactions

Monitor

monitor renal function and for skin toxicities

Use with caution and monitor for adverse effects.

✗

pediatric_age

pediatric
unsafe
FDA Category
N
Dose Adjustment

not established

Key Recommendations

not approved for use in pediatric patients

Monitor

not applicable

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

⚠

renal_impairment

severe renal impairment
caution
FDA Category
N
Dose Adjustment

no dose adjustment required based on pharmacokinetics

Key Recommendations

use with caution in patients with severe renal impairment

Monitor

monitor renal function during treatment

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate hepatic impairment
caution
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

use with caution in patients with hepatic impairment including bilirubin elevation

Monitor

monitor liver function tests regularly

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classFDA
2023

Drug class

Value:Monoclonal antibody (EGFR inhibitor)

Panitumumab is a fully human monoclonal antibody that targets the epidermal growth factor receptor (EGFR)

prescribingFDA
2023

FDA approval year

Value:2006

Initial FDA approval date for Panitumumab (Vectibix)

usageNCCN
2023

Common uses

Value:Metastatic colorectal cancer with wild-type KRAS gene

Primary therapeutic indication for Panitumumab

mechanismFDA
2023

Mechanism of action

Value:EGFR antagonist

Binds to EGFR to block ligand-induced receptor activation

Panitumumab is indicated for the treatment of patients with wild-type RAS metastatic colorectal cancer, either as monotherapy or in combination with chemotherapy. It is typically used in patients who have progressed on or after fluoropyrimidine-, oxaliplatin-, and irinotecan-containing chemotherapy regimens.

Panitumumab is a fully human IgG2 monoclonal antibody that binds specifically to the extracellular domain of EGFR. By binding to EGFR, it prevents activation by endogenous ligands (such as EGF and TGF-alpha), blocking receptor dimerization and subsequent intracellular signaling cascades. This inhibition of the RAS/RAF/MAPK and PI3K/AKT pathways results in reduced cell proliferation, apoptosis, and inhibited tumor invasion/metastasis.

Common side effects include dermatologic toxicities such as acneiform rash, dry skin, and pruritus (occurring in over 80% of patients), which correlate with treatment efficacy. Hypersensitivity and infusion-related reactions may occur. Electrolyte abnormalities, particularly hypomagnesemia, require monitoring. Panitumumab is contraindicated in patients with wild-type RAS tumors and requires KRAS/RAS testing prior to treatment initiation.

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