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An Amendment to the FLAIR Study to Evaluate the Pharmacokinetics, Safety, Tolerability, Maintenance of Virological Suppression and Patient Reported Outcomes for Participants Receiving Cabotegravir (CAB 200 mg/mL) and Rilpivirine (300 mg/mL) Long-Acting Injections Following Sub-cutaneous (SC) Administration in the Anterior Abdominal Wall SC Tissue Compared With Intramuscular (IM) Administration in the Gluteus Medius Muscle in Adult Participants Living With HIV-1 Infection in the FLAIR Study

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Trial Profile

An Amendment to the FLAIR Study to Evaluate the Pharmacokinetics, Safety, Tolerability, Maintenance of Virological Suppression and Patient Reported Outcomes for Participants Receiving Cabotegravir (CAB 200 mg/mL) and Rilpivirine (300 mg/mL) Long-Acting Injections Following Sub-cutaneous (SC) Administration in the Anterior Abdominal Wall SC Tissue Compared With Intramuscular (IM) Administration in the Gluteus Medius Muscle in Adult Participants Living With HIV-1 Infection in the FLAIR Study

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 28 Nov 2024

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At a glance

  • Drugs Cabotegravir (Primary) ; Rilpivirine (Primary)
  • Indications HIV-1 infections
  • Focus Pharmacokinetics; Registrational
  • Sponsors ViiV Healthcare

Most Recent Events

  • 21 Dec 2023 Status changed from active, no longer recruiting to completed.
  • 13 Jun 2023 New trial record

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