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A multi-center, randomized, double-blind, active-control, 96 week, phase III trial of the efficacy and safety of clevudine compared with adefovir at weeks 48 and 96 in nucleoside treatment-naive patients with HBeAg negative chronic hepatitis due to hepatitis B virus

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A multi-center, randomized, double-blind, active-control, 96 week, phase III trial of the efficacy and safety of clevudine compared with adefovir at weeks 48 and 96 in nucleoside treatment-naive patients with HBeAg negative chronic hepatitis due to hepatitis B virus

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 12 Apr 2022

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At a glance

  • Drugs Clevudine (Primary) ; Adefovir
  • Indications Hepatitis B
  • Focus Registrational; Therapeutic Use
  • Acronyms QUASH-2
  • Sponsors Pharmasset

    • Most Recent Events

    • 08 Apr 2022 This trial has been completed in Spain (End Date: 31 May 2009), according to European Clinical Trials Database record.
    • 20 Apr 2009 Status changed from recruiting to discontinued, according to Pharmasset media release.
    • 08 Jul 2008 Pharmasset plans to submit the 48-week data from this study to the FDA as a basis for clevudine marketing approval.

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