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A Phase 2/3, Open-Label Study of the Pharmacokinetics, Safety, and Antiviral Activity of the GS-9883/Emtricitabine/Tenofovir Alafenamide (GS-9883/F/TAF) Fixed Dose Combination (FDC) in HIV-1 Infected Adolescents and Children

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Trial Profile

A Phase 2/3, Open-Label Study of the Pharmacokinetics, Safety, and Antiviral Activity of the GS-9883/Emtricitabine/Tenofovir Alafenamide (GS-9883/F/TAF) Fixed Dose Combination (FDC) in HIV-1 Infected Adolescents and Children

Status: Recruiting
Phase of Trial: Phase II/III

Latest Information Update: 03 Jun 2024

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At a glance

  • Drugs Bictegravir/emtricitabine/tenofovir alafenamide (Primary)
  • Indications HIV-1 infections
  • Focus Adverse reactions; Pharmacokinetics; Registrational
  • Sponsors Gilead Sciences
  • Most Recent Events

    • 25 Apr 2024 According to a Gilead Sciences media release, data from this study were presented at the 31st Conference on Retroviruses and Opportunistic Infections (CROI).
    • 31 Jan 2023 Planned number of patients changed from 125 to 172.
    • 31 Jan 2023 Status changed from active, no longer recruiting to recruiting.

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