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  • Patient Profiles
    • Early Switch Patients
    • Established Switch Patients
  • Efficacy & Safety
    • CABENUVA vs BIKTARVY
    • Every-2-Month vs Once-Monthly CABENUVA
    • Once-Monthly CABENUVA vs Daily Oral Therapy
    • Real-World Study | CABENUVA & BIKTARVY
    • Real-World Long-Term Data | Switch to CABENUVA
    • Early Switch to Every-2-Month CABENUVA
    • Resistance & CVF
  • Additional Considerations
    • Real-World Adherence
    • OPERA Retention in Care
    • VOLITION Choice Data
    • Patient Preference
  • In Your Practice
    • Dosing & Administration
    • Patient Savings
    • Starter Sample Program
    • Access & Acquisition
    • Home
    • Patient Profiles
      • Early Switch Patients
      • Established Switch Patients
    • Efficacy & Safety
      • CABENUVA vs BIKTARVY
      • Every-2-Month vs Once-Monthly CABENUVA
      • Once-Monthly CABENUVA vs Daily Oral Therapy
      • Real-World Study | CABENUVA & BIKTARVY
      • Real-World Long-Term Data | Switch to CABENUVA
      • Early Switch to Every-2-Month CABENUVA
      • Resistance & CVF
    • Additional Considerations
      • Real-World Adherence
      • OPERA Retention in Care
      • VOLITION Choice Data
      • Patient Preference
    • In Your Practice
      • Dosing & Administration
      • Patient Savings
      • Starter Sample Program
      • Access & Acquisition

    PMUS-CBRWCNT260019

    INDICATION

    CABENUVA is indicated as a complete regimen for the treatment of HIV-1 infection in adults and adolescents 12 years of age and older and weighing at least 35 kg to replace the current antiretroviral regimen in those who are virologically suppressed (HIV-1 RNA <50 copies/mL) on a stable antiretroviral regimen with no history of treatment failure and with no known or suspected resistance to either cabotegravir or rilpivirine.

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    PMUS-CBRWCNT260019 September 2026
    Produced in USA.

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