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A Phase III Double-blind, Randomised, Parallel Group Comparison of the Efficacy and Safety of FP-1201-lyo (Recombinant Human Interferon Beta-1a) and Placebo in the Treatment of Patients with Moderate or Severe Acute Respiratory Distress Syndrome

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A Phase III Double-blind, Randomised, Parallel Group Comparison of the Efficacy and Safety of FP-1201-lyo (Recombinant Human Interferon Beta-1a) and Placebo in the Treatment of Patients with Moderate or Severe Acute Respiratory Distress Syndrome

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 28 Mar 2022

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At a glance

  • Drugs Interferon beta-1a (Primary)
  • Indications Adult respiratory distress syndrome
  • Focus Registrational; Therapeutic Use
  • Acronyms INTEREST
  • Sponsors Faron Pharmaceuticals

    • Most Recent Events

    • 26 Mar 2022 This trial is completed in Belgium (End Date: 23 May 2018), according to European Clinical Trials Database record.
    • 20 May 2020 According to a Faron Pharmaceuticals media release, results of this study have been published in Intensive Care Medicine
    • 17 Feb 2020 Primary endpoint (Efficacy Endpoint: Days free of mechanical ventilation) has not been met published in the JAMA: the Journal of the American Medical Association

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