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A Phase I/II Trial to Evaluate the Safety and Tolerability of Ides (IgG Endopeptidase) to Eliminate Donor Specific HLA Antibodies (DSAs) and Prevent Antibody-Mediated Rejection Post-Transplant in Highly-HLA Sensitized Patients.

Trial Profile

A Phase I/II Trial to Evaluate the Safety and Tolerability of Ides (IgG Endopeptidase) to Eliminate Donor Specific HLA Antibodies (DSAs) and Prevent Antibody-Mediated Rejection Post-Transplant in Highly-HLA Sensitized Patients.

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 14 Jul 2023

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At a glance

  • Drugs Imlifidase (Primary)
  • Indications Renal transplant rejection
  • Focus Registrational; Therapeutic Use
  • Most Recent Events

    • 11 Jul 2023 According to a Hansa Biopharma AB media release, the Australian Therapeutic Goods Administration ("TGA") has provisionally approved Idefirix (imlifidase) as desensitization treatment for highly sensitized patients prior to kidney transplantation from both living and deceased donors. The provisional approval has a duration of two years and was based on data from Hansa's phase 2 studies.
    • 26 Oct 2018 Results presented in a Hansa Medical AB media release.
    • 26 Oct 2018 According to a Hansa Medical AB media release, the data from this study was highlighted in a presentation at the American Society of Nephrology (ASN) Kidney Week 2018.
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