Safety and pharmacokinetics of intravenous zanamivir treatment in hospitalized adults with influenza: an open-label, multicenter, single-arm, phase II study

Marty, F. M.; Man, C. Y.; Van der Horst, C.; Francois, B.; Garot, D.; Mánez, R.; Thamlikitkul, V.; Lorente Balanza, José Ángel; Álvarez Lerma, Francisco; Brealey, D.; Zhao, H. H.; Weller, S.; Yates, P. J.; Peppercorn, A. F.

doi:10.1093/infdis/jit467

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Safety and pharmacokinetics of intravenous zanamivir treatment in hospitalized adults with influenza: an open-label, multicenter, single-arm, phase II study

Marty, F. M.; Man, C. Y.; Van der Horst, C.; Francois, B.; Garot, D.; Mánez, R.; Thamlikitkul, V.; Lorente Balanza, José Ángel; Álvarez Lerma, Francisco; Brealey, D.; Zhao, H. H.; Weller, S.; Yates, P. J.; Peppercorn, A. F.

Use este identificador para citar o enlazar este ítem: http://hdl.handle.net/11268/4210

Fecha: 2014

Materia UNESCO: Investigación médica

Tipo: article

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Resumen:

Intravenous zanamivir is a neuraminidase inhibitor suitable for treatment of hospitalized patients with severe influenza. Patients were treated with intravenous zanamivir 600 mg twice daily, adjusted for renal impairment, for up to 10 days. Primary outcomes included adverse events (AEs), and clinical/laboratory parameters. Pharmacokinetics, viral load, and disease course were also assessed.

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