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Research programme: gene therapy for hearing disorders - SalioGen Therapeutics

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Drug Profile

Research programme: gene therapy for hearing disorders - SalioGen Therapeutics

Latest Information Update: 24 Aug 2021

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At a glance

  • Originator SalioGen Therapeutics
  • Class Eye disorder therapies; 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

  • Research Usher syndromes

Most Recent Events

  • 10 Aug 2021 Early research in Usher syndromes in USA (Parenteral) before August 2021 (SalioGen Therapeutics pipeline, August 2021)

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