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Multicenter, Double-blind, Parallel-group, Randomized, 48 Weeks, Dose-ranging, Placebo-controlled Phase II Trial to Evaluate Efficacy, Safety and Tolerability of Multiple Subcutaneous (s.c.) Doses of BI 456906 in Patients With Non-alcoholic Steatohepatitis (NASH) and Fibrosis

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Multicenter, Double-blind, Parallel-group, Randomized, 48 Weeks, Dose-ranging, Placebo-controlled Phase II Trial to Evaluate Efficacy, Safety and Tolerability of Multiple Subcutaneous (s.c.) Doses of BI 456906 in Patients With Non-alcoholic Steatohepatitis (NASH) and Fibrosis

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 12 Jun 2024

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At a glance

  • Drugs Survodutide (Primary)
  • Indications Hepatic fibrosis; Non-alcoholic steatohepatitis
  • Focus Therapeutic Use
  • Sponsors Boehringer Ingelheim

    • Most Recent Events

    • 07 Jun 2024 Results presented in a Zealand Pharma Media Release.
    • 07 Jun 2024 According to Boehringer Ingelheim Media Release, data from this trial published in The New England Journal of Medicine
    • 07 Jun 2024 According to Boehringer Ingelheim Media Release, data from this trial presented today at the European Association for the Study of the Liver Congress (EASL) 2024
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