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A single-dose, randomized, open-label, 2-period crossover study to evaluate the bioequivalence of the ACC008 (test formulation [T]) versus coadministered ainuovirine (ANV) 150 mg, lamivudine (3TC) 300 mg, and tenofovir disoproxil fumarate 300 mg (reference formulation [R]) in the fasted state among the Chinese healthy adults

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A single-dose, randomized, open-label, 2-period crossover study to evaluate the bioequivalence of the ACC008 (test formulation [T]) versus coadministered ainuovirine (ANV) 150 mg, lamivudine (3TC) 300 mg, and tenofovir disoproxil fumarate 300 mg (reference formulation [R]) in the fasted state among the Chinese healthy adults

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 22 Jan 2024

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At a glance

  • Drugs Ainuovirine (Primary) ; Ainuovirine/lamivudine/tenofovir (Primary) ; Lamivudine (Primary) ; Tenofovir disoproxil fumarate (Primary)
  • Indications HIV infections
  • Focus Adverse reactions; Pharmacokinetics

    • Most Recent Events

    • 22 Jan 2024 New trial record
    • 01 Jan 2024 Results published in the Clinical Pharmacology in Drug Development

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