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A Phase 2 Randomized, Dose-Titration, Open-Label Study Evaluating the Safety and Efficacy of BIV201 Compared to Standard of Care to Reduce Ascites and Complications in Cirrhotic Patients With Refractory Ascites

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Trial Profile

A Phase 2 Randomized, Dose-Titration, Open-Label Study Evaluating the Safety and Efficacy of BIV201 Compared to Standard of Care to Reduce Ascites and Complications in Cirrhotic Patients With Refractory Ascites

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 29 Dec 2023

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At a glance

  • Drugs Terlipressin (Primary)
  • Indications Ascites
  • Focus Adverse reactions; Registrational
  • Sponsors BioVie

    • Most Recent Events

    • 14 Nov 2023 Results reporting safety profile of BIV201 presented at The Liver Meeting 2023: 74th Annual Meeting of the American Association for the Study of Liver Diseases
    • 13 Nov 2023 According to BioVie media release, clinical safety data from this trial will be presented at the American Association for the Study of Liver Diseases (AASLD) - The Liver Meeting 2023 in Boston, MA.
    • 05 Jul 2023 Status changed from active, no longer recruiting to discontinued.

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