How frequently should Apretude (cabotegravir) be administered for HIV pre‑exposure prophylaxis?

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Apretude Injection Dosing Schedule

Apretude (cabotegravir) is administered as 600 mg intramuscular gluteal injections with the first two injections separated by 4 weeks, followed by injections every 8 weeks (every 2 months) thereafter. 1

Initial Dosing Phase

  • The first injection is 600 mg (3 mL) administered intramuscularly in the gluteal muscle 1
  • The second injection is given exactly 4 weeks (1 month) after the first injection 1
  • This initial 4-week interval establishes adequate drug levels before transitioning to the maintenance schedule 2

Maintenance Dosing Phase

  • After the first two injections, all subsequent injections are given every 8 weeks (every 2 months) 1
  • Each maintenance injection is 600 mg (3 mL) administered intramuscularly in the gluteal region 1
  • This results in only 6 injections per year after the initial loading phase 2

Managing Missed or Delayed Injections

If an injection is less than 8 weeks late: Resume injections as soon as possible after confirming negative HIV testing, and continue with the every-8-week schedule 1

If an injection is 8 or more weeks late: You must restart the loading phase with two injections separated by 4 weeks before returning to the every-8-week maintenance schedule 1. This "reloading" is critical because drug concentrations may have fallen below protective levels.

Mandatory HIV Testing Before Every Injection

  • Perform a rapid point-of-care HIV antibody test on the day of each injection before administering the dose 1
  • Send a laboratory-based fourth- or fifth-generation combination antigen/antibody test, but do not delay the injection while waiting for results 1
  • This testing is non-negotiable because cabotegravir can delay HIV seroconversion and mask early infection, potentially leading to integrase inhibitor resistance if HIV is acquired 3, 4

Critical Safety Considerations

Never skip pre-injection HIV testing, even if the patient appears low-risk or was recently tested, as undetected HIV infection during cabotegravir exposure creates high risk for multi-drug resistant virus 3. The long half-life of cabotegravir (approximately 47 days after injection) means subtherapeutic drug levels can persist for months, creating an ideal environment for resistance development if HIV is acquired 5, 6.

Injection site reactions occur in up to 81% of patients but are typically mild and decrease in severity over subsequent injections 7. These should be managed with topical and systemic analgesics and hot or cold packs 1.

Additional Monitoring Requirements

  • STI screening should be performed every 4 months (at every second injection) 1
  • Liver enzyme tests should be administered every 6 months 1
  • Serum creatinine and estimated creatinine clearance are required at baseline 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Counseling on Seroconversion Risk for Patients Starting Cabotegravir PrEP

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Contraindications and Cautions for Cabotegravir PrEP

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Cabotegravir for HIV Prevention in Cisgender Men and Transgender Women.

The New England journal of medicine, 2021

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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