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Acoramidis

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

Acoramidis is a selective transthyretin stabilizer used in the treatment of transthyretin amyloidosis, a progressive disease where abnormal amyloid protein deposits accumulate in organs such as the heart and peripheral nervous system. By binding to thyroxine binding sites on transthyretin, the medication prevents the protein tetramer from dissociating into monomers, thereby blocking the initial step in amyloid fibril formation.

Quick summary

Acoramidis stabilizes the transthyretin protein to prevent amyloid formation in patients with transthyretin amyloidosis.

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

Key facts at a glance

ATC
C01EB25
RxNorm
2698312
Generic
Acoramidis
Class
atc-c01
Brands
Attruby
Availability
rx
Lactation
unknown
Routes
oral
Forms
tablet
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
800mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
not established
Maximum
consult physician
Frequency
not established
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
800mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose exceeding 10000 mg may cause serious toxicity based on general pharmacological considerations
Chronic overdose: cumulative doses significantly exceeding recommended 711 mg twice daily over extended periods may lead to organ toxicity
Immediate actions
activated charcoal within 1-2 hours of ingestion, gastric lavage if within 1 hour, supportive care, continuous cardiac monitoring
Antidote
no specific antidote identified(supportive care is primary treatment; no specific antidote demonstrated effective)
Poison Control: 1-800-222-1222

Special Populations

10 groups
?

pregnancy

first trimester
unknown
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if potential benefits outweigh potential risks to the fetus

Monitor

regular fetal monitoring recommended

?

pregnancy

second trimester
unknown
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if potential benefits outweigh potential risks to the fetus

Monitor

regular fetal monitoring recommended

?

pregnancy

third trimester
unknown
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if potential benefits outweigh potential risks to the fetus

Monitor

regular fetal monitoring and assessment of labor

?

lactation

breastfeeding
unknown
FDA Category
N
Dose Adjustment

avoid

Key Recommendations

discontinue breastfeeding or avoid drug; decision should be made considering benefit of breastfeeding to infant and benefit of drug to mother

Monitor

monitor infant for adverse effects

⚠

geriatric

elderly 65 and older
caution
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

no dose adjustment required based on age alone; use with caution due to potential comorbidities and concomitant medications

Monitor

monitor renal and hepatic function periodically

Use with caution and monitor for adverse effects.

✗

pediatric_age

children and adolescents
unsafe
FDA Category
N
Dose Adjustment

not applicable

Key Recommendations

not indicated for use in pediatric patients; 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 renal impairment
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

no dose adjustment required for mild renal impairment

Monitor

routine monitoring not required

⚠

renal_impairment

moderate severe renal impairment
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

use with caution; limited data available for severe renal impairment

Monitor

monitor renal function periodically

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild hepatic impairment
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

use with caution; limited data available

Monitor

monitor hepatic function

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate severe hepatic impairment
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

use with caution; not studied in severe hepatic impairment

Monitor

monitor hepatic function and for adverse effects

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2023

FDA approval for Attruby (acoramidis) for ATTR cardiomyopathy

drug_classFDA
2023

Drug class

Value:Transthyretin (TTR) stabilizer

Mechanism of action classification

usageFDA
2023

Primary indication

Value:ATTR cardiomyopathy (transthyretin amyloidosis)

Therapeutic indication for Attruby

clinical_trialsClinicalTrials.gov
2023

Key trial name

Value:ATTRIBUTE-CM

Pivotal clinical trial supporting FDA approval

Treatment of transthyretin amyloidosis (ATTR), including hereditary transthyretin amyloid polyneuropathy (ATTRv-PN) and transthyretin amyloid cardiomyopathy (ATTR-CM), both wild-type and mutant forms.

Acoramidis is a selective TTR stabilizer that binds to thyroxine binding sites on transthyretin tetramers. This binding prevents dissociation into monomers, which is the rate-limiting step in amyloidogenesis, thereby reducing amyloid fibril formation.

Acoramidis is taken orally. Common side effects may include gastrointestinal symptoms. Patients should be monitored for liver function and cardiac status. The medication should be used as prescribed by a specialist experienced in treating amyloidosis.

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