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Safety, Tolerability and Efficacy of Monoclonal CD38 Antibody Felzartamab in Late Antibody-Mediated Renal Allograft Rejection - A Phase 2 Pilot Trial

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Trial Profile

Safety, Tolerability and Efficacy of Monoclonal CD38 Antibody Felzartamab in Late Antibody-Mediated Renal Allograft Rejection - A Phase 2 Pilot Trial

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 16 Oct 2024

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At a glance

  • Drugs Felzartamab (Primary)
  • Indications Renal transplant rejection
  • Focus Adverse reactions
  • Acronyms Felzartamab in late ABMR
  • Most Recent Events

    • 09 Oct 2024 According to Biogen media release, Felzartamab has received Breakthrough Therapy Designation (BTD) from the U.S. Food and Drug Administration (FDA) for the treatment of late antibody-mediated rejection (AMR) without T-cell mediated rejection in kidney transplant patients
    • 30 May 2024 According to an OncoCyte Corporation Media Release, company will be hosting a conference call to discuss the results of the clinical trial with study authors, Dr. Klemens Budde, Head of Transplantation at Charite, and Dr. Ekke Schuetz, Chief Science Officer at Oncocyte.The date and time of the call will be announced in due course.
    • 30 May 2024 According to an OncoCyte Corporation Media Release, data from this study will be presented at a Late Breaking Abstract at the 2024 American Transplant Congress on June 3rd 2024 at 9:15 ET

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