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Cabotegravir

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

Cabotegravir is a long-acting antiretroviral medication used in combination with rilpivirine (as CABENUVA) for the treatment of HIV-1 infection in adults. It is administered as an injectable formulation, providing an alternative to daily oral antiretroviral therapy. This medication is used as a complete regimen for maintaining viral suppression in patients who are virologically stable.

Quick summary

Cabotegravir is a long-acting injectable antiretroviral used with rilpivirine to treat HIV-1 infection in adults, offering an alternative to daily oral medication.

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

Key facts at a glance

ATC
J05AJ04
RxNorm
2475077
Generic
Cabotegravir
Class
atc-j05
Brands
Vocabria, Apretude
Availability
rx
Lactation
unknown
Routes
oral
Forms
injection, 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
30mg once daily
Maximum
consult physician
Frequency
once daily (with rilpivirine)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
adult (standard)injectable suspension
Usual dose
600mg every 2 months (after loading dose)
Maximum
consult physician
Frequency
every 8 weeks (initially: week 0, week 4, then q8w)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
adult (pre-exposure prophylaxis (PrEP))injectable suspension
Usual dose
600mg every 2 months
Maximum
consult physician
Frequency
every 8 weeks (month 0, month 1, then q8w)
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Specific toxic single dose for cabotegravir has not been established in clinical literature
Chronic overdose: cumulative toxicity information not well characterized
Immediate actions
supportive care; monitor vital signs; consider gastric decontamination if ingestion is recent
Antidote
no specific antidote exists(supportive care is primary treatment approach)
Poison Control: 1-800-222-1222

Special Populations

8 groups
⚠

pregnancy

first trimester
caution
FDA Category
B
Dose Adjustment

use only if benefits outweigh risks

Key Recommendations

cabotegravir should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus

Monitor

regular prenatal monitoring and fetal assessment

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
B
Dose Adjustment

use only if benefits outweigh risks

Key Recommendations

continue therapy only if benefits outweigh potential risks

Monitor

routine prenatal care and fetal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
B
Dose Adjustment

use only if benefits outweigh risks

Key Recommendations

consider continuing for maternal HIV prevention until delivery

Monitor

routine prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

avoid or discontinue breastfeeding

Key Recommendations

cabotegravir is excreted in breast milk; breastfeeding should be avoided in HIV-positive mothers to prevent transmission

Monitor

infant monitoring for adverse effects

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly 65 plus
caution
FDA Category
N
Dose Adjustment

no specific dose adjustment required

Key Recommendations

use with caution due to limited clinical trial data in patients over 65 years

Monitor

regular assessment of renal and hepatic function

Use with caution and monitor for adverse effects.

✓

pediatric_age

adolescents 12 17
safe
FDA Category
B
Dose Adjustment

no dose adjustment required

Key Recommendations

approved for use in adolescents 12 years and older for HIV PrEP

Monitor

regular monitoring of HIV status and adverse effects

⚠

renal_impairment

severe renal impairment
caution
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

use with caution; cabotegravir is not significantly renally cleared

Monitor

monitor renal function periodically

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; cabotegravir is not significantly metabolized by hepatic enzymes

Monitor

monitor liver function tests

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classWHO
2023

Drug class

Value:HIV integrase inhibitor (antiretroviral)

Drug class information for Cabotegravir

prescribingFDA
2023

FDA approval year for PrEP

Value:2021

FDA approval of Apretude for HIV pre-exposure prophylaxis

usageCDC
2023

Primary indication

Value:HIV pre-exposure prophylaxis (PrEP) and HIV treatment

Primary therapeutic uses of Cabotegravir

formulationFDA
2023

Available formulations

Value:Oral tablets (Vocabria) and long-acting injectable (Apretude)

Formulation types available for Cabotegravir

Cabotegravir (as part of CABENUVA with rilpivirine) is indicated for the treatment of HIV-1 infection in adults who are virologically stable and suppressed. It is used as a complete regimen for maintenance therapy, offering an alternative to daily oral antiretroviral treatment.

Cabotegravir is an integrase strand transfer inhibitor (INSTI) that works by binding to the integrase enzyme and blocking the strand transfer step of viral DNA integration into host cell DNA, preventing HIV replication.

Cabotegravir is administered as long-acting monthly or every-other-month intramuscular injections by a healthcare provider. Missing doses can lead to viral resistance, so adherence to the injection schedule is critical. Patients must be carefully selected and monitored for potential drug interactions and injection site reactions.

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