A Phase I/II Open-Label Study to Assess the Safety, Tolerability and Preliminary Efficacy of FP-1201 (Recombinant Human Interferon Beta) in the Treatment of Patients With Acute Lung Injury and Acute Respiratory Distress Syndrome.

Trial Profile

A Phase I/II Open-Label Study to Assess the Safety, Tolerability and Preliminary Efficacy of FP-1201 (Recombinant Human Interferon Beta) in the Treatment of Patients With Acute Lung Injury and Acute Respiratory Distress Syndrome.

Completed
Phase of Trial: Phase I/II

Latest Information Update: 13 Jun 2016

At a glance

  • Drugs Interferon beta-1a (Primary)
  • Indications Acute lung injury; Respiratory distress syndrome
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Faron Pharmaceuticals
  • Most Recent Events

    • 13 Jun 2016 Data from this trial were published in The Lancet Respiratory Medicine in 2014, according to a Faron Pharmaceuticals media release.
    • 20 May 2015 Results published in a Faron media release.
    • 16 Oct 2014 According to a Faron Pharmaceuticals, this study is part of Traumakine programm.
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