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Research programme: AAV vector based gene therapies - Abeona Therapeutics

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Drug Profile

Research programme: AAV vector based gene therapies - Abeona Therapeutics

Alternative Names: AIM™ vectors

Latest Information Update: 02 Apr 2024

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At a glance

  • Originator University of North Carolina at Chapel Hill
  • Developer Abeona Therapeutics
  • Class Gene therapies
  • Mechanism of Action Gene transference
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity No

Highest Development Phases

  • Preclinical Eye disorders
  • No development reported CNS disorders; Fabry's disease; Glycogen storage disease type II

Most Recent Events

  • 18 Mar 2024 Abeona Therapeutics files for patent protection with national authorities of US, Europe and other geographical regions for a second patent family directed to certain AAV capsids
  • 18 Mar 2024 Abeona Therapeutics has patent protection for a patent family covering novel AAV capsids in US, Australia, Israel, Russia
  • 28 Feb 2023 No recent reports of development identified for preclinical development in Fabry's-disease in USA (IV)

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