Treatment of Primary Sjogren's Syndrome with Low-Dose Natural Human Interferon-alpha Administered by the Oral Mucosal Route: A Phase II Clinical Trial

The purpose of this investigation was to examine the safety and efficacy of four dosages of natural human interferon-alpha (nHuIFN-alpha) delivered over a 12-week period orally in lozenges (150 IU and 450 IU, once [QD] or three times [TID] daily) compared to placebo in subjects with primary Sjögren&...

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Veröffentlicht in:Journal of interferon & cytokine research 1999-08, Vol.19 (8), p.943-951
Hauptverfasser: Ship, Jonathan A., Fox, Philip C., Michalek, Joel E., Cummins, Martin J., Richards, Alan B., Group, IFN Protocol Study
Format: Artikel
Sprache:eng
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