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Research programme: colour vision defects gene therapy - Adverum/University of Washington

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Drug Profile

Research programme: colour vision defects gene therapy - Adverum/University of Washington

Alternative Names: AVA-322; AVA-323; Colour blindness gene therapy - Adverum/University of Washington; L-opsin gene therapy; M-opsin gene therapy

Latest Information Update: 28 Oct 2019

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At a glance

  • Originator Avalanche Biotechnologies; University of Washington
  • Developer Adverum Biotechnologies; University of Washington
  • 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

  • No development reported Colour vision defects

Most Recent Events

  • 28 Oct 2019 No recent reports of development identified for preclinical development in Colour-vision-defects in USA (Intravitreous)
  • 13 Aug 2015 Preclinical trials in Colour vision defects in USA (Intravitreous) before August 2015
  • 25 Mar 2015 Avalanche Biotechnologies and University of Washington agree to co-develop gene therapy for Colour vision defects

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