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A Phase II Study to Evaluate the Safety, Tolerability, Efficacy and Pharmacokinetics of Intravenous Ascending Doses of IdeS in Kidney Transplantation

Trial Profile

A Phase II Study to Evaluate the Safety, Tolerability, Efficacy and Pharmacokinetics of Intravenous Ascending Doses of IdeS in Kidney Transplantation

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 18 Sep 2019

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At a glance

  • Drugs Imlifidase (Primary)
  • Indications Renal transplant rejection
  • Focus Adverse reactions
  • Sponsors Hansa Biopharma AB; Hansa Medical AB
  • Most Recent Events

    • 18 Sep 2019 According to a Hansa Biopharma AB media release, pooled data from this and other three studies (230633, 269806 and 305829) were presented at the 19th Congress of the European Society for Organ Transplantation (ESOT) 2019 in Copenhagen, Denmark.
    • 03 Aug 2017 Combined results of trials ( NCT02224820, NCT02426684, NCT02475551) assessing the efficacy of IdeS with regard to desensitization and transplantation of a kidney from an HLA-incompatible donor.published in the New England Journal of Medicine
    • 02 Aug 2017 According to a Hansa Medical media release, combined results from this and 2 other trials (CT 230633 and 256416) have been published in the New England Journal of Medicine.
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