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Avutometinib Potassium (Ojjaara): Patient Guide

Published: July 26, 2026Updated: August 24, 2026

Avutometinib potassium is a prescription targeted therapy for symptomatic plexiform neurofibromas, which are tumor growths associated with neurofibromatosis type 1 (NF1). It is taken by mouth and is approved for adults and children 2 years of age and older.

Quick summary

Avutometinib potassium may help shrink or relieve symptoms of NF1-related plexiform neurofibromas. Take it exactly as prescribed and contact your doctor or pharmacist about side effects, pregnancy, and other medicines.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 24, 2026Editorial policy

Key facts at a glance

RxNorm
2714514
Generic
Avutometinib Potassium
Class
pin-variant
Brands
—
Availability
rx
Lactation
unknown
Routes
—
Forms
—
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: Consult local poison control center for specific information
Chronic overdose: Varies by patient
Immediate actions
Call poison control center: 1-800-222-1222
Poison Control: 1-800-222-1222

Special Populations

11 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 via ultrasound

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

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; consider timing of delivery

Monitor

regular fetal monitoring and biophysical profiles

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

✗

lactation

breastfeeding
unsafe
FDA Category
N
Dose Adjustment

avoid

Key Recommendations

discontinue breastfeeding during treatment and for at least 2 weeks after last dose

Monitor

N/A

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

?

pediatric_age

children under 12
unknown
FDA Category
N
Dose Adjustment

safety and efficacy not established

Key Recommendations

use only in clinical trials or if benefits outweigh potential risks

Monitor

close monitoring for growth and development

⚠

pediatric_age

adolescents 12 17
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

use only if potential benefits outweigh risks; monitor growth plates

Monitor

regular assessment of growth and skeletal development

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly over 65
caution
FDA Category
N
Dose Adjustment

no specific dose adjustment required; start at lower end of dosing range

Key Recommendations

use with caution; monitor for adverse effects including fatigue and GI symptoms

Monitor

regular monitoring of renal and hepatic function

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild
caution
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

monitor renal function periodically

Monitor

baseline and periodic creatinine clearance monitoring

Use with caution and monitor for adverse effects.

⚠

renal_impairment

moderate
caution
FDA Category
N
Dose Adjustment

consider dose reduction

Key Recommendations

use with caution; consider dose reduction based on tolerability

Monitor

close monitoring of renal function and drug tolerability

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild
caution
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

use with caution; monitor liver enzymes

Monitor

baseline and periodic liver function tests

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate
caution
FDA Category
N
Dose Adjustment

consider dose reduction

Key Recommendations

use with caution; dose reduction may be required

Monitor

frequent monitoring of liver function and bilirubin

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classNCI
2023

Drug class

Value:MEK inhibitor

Avutometinib is a mitogen-activated extracellular signal-regulated kinase kinase (MEK) inhibitor

development_statusClinicalTrials.gov
2023

Development status

Value:Experimental

Avutometinib Potassium is currently in clinical trials and not yet FDA approved

mechanismFDA
2023

Mechanism of action

Value:MAPK pathway inhibition

Inhibits MEK1/2 kinase activity to block RAS/RAF/MEK/ERK signaling pathway

therapeutic_areaNIH
2023

Primary investigation area

Value:Oncology

Being studied for treatment of various solid tumors including pancreatic, ovarian, and lung cancers

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 August 24, 2026. · Read our editorial policy