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A Phase I Single Center Study to Evalute the Safety, Tolerability and Pharmacokinetics of Intravenous IdeS After Administration of Single Ascending Doses in Healthy Male Subjects

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Trial Profile

A Phase I Single Center Study to Evalute the Safety, Tolerability and Pharmacokinetics of Intravenous IdeS After Administration of Single Ascending Doses in Healthy Male Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 29 Mar 2019

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At a glance

  • Drugs Imlifidase (Primary)
  • Indications Transplant rejection
  • Focus Adverse reactions; First in man; Proof of concept
  • Sponsors Hansa Biopharma AB; Hansa Medical AB

Most Recent Events

  • 16 Jul 2015 According to Hansa Medical AB media release, results have been published in PLOS ONE.
  • 16 Jul 2015 Results published in Hansa Medical AB media release.
  • 18 Feb 2015 Results published in Hansa Medical AB media release.

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