Breda, the Netherlands / Ghent, Belgium

  • Trial met primary endpoint (p ˂0.0001)
  • Well-tolerated; safety profile comparable to placebo
  • Biologics License Application on track to be submitted to U.S. Food and Drug Administration by end of 2020
  • Conference call scheduled for today, May 26, 2020 at 8:30 a.m. EDT (2:30 p.m. CEST)

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arGEN-X SE published this content on 26 May 2020 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 24 June 2020 14:23:40 UTC