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A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study Investigating the Safety, Tolerability, and Pharmacokinetics of Intravenously Administered REGN3470-3471-3479 in Healthy Adult Subjects

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Trial Profile

A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study Investigating the Safety, Tolerability, and Pharmacokinetics of Intravenously Administered REGN3470-3471-3479 in Healthy Adult Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 06 Nov 2021

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At a glance

  • Drugs Atoltivimab/maftivimab/odesivimab (Primary)
  • Indications Ebola virus infections
  • Focus Adverse reactions; First in man
  • Sponsors Regeneron Pharmaceuticals

    • Most Recent Events

    • 02 Oct 2017 Status changed from active, no longer recruiting to completed, according to a Regeneron pharmaceuticals media release.
    • 05 Aug 2016 According to a Regeneron media release, in the second quarter of 2016, the USFDA has granted orphan-drug designation to REGN3470-3471-3479 for the treatment of Ebola virus infection.
    • 23 Jun 2016 Status changed from not yet recruiting to recruiting.

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