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Research programme: gene therapies expressing intracellular proteins - Clearside Biomedical

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Drug Profile

Research programme: gene therapies expressing intracellular proteins - Clearside Biomedical

Latest Information Update: 28 Sep 2024

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At a glance

  • Originator Clearside Biomedical
  • 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

  • No development reported Stargardt disease; Usher syndromes

Most Recent Events

  • 28 Sep 2024 No recent reports of development identified for preclinical development in Usher-syndromes in USA (Intraocular, Injection)
  • 28 Mar 2023 No recent reports of development identified for preclinical development in Stargardt disease in USA (Intraocular, Injection)
  • 12 Feb 2019 Preclinical trials in Stargardt disease in USA (Intraocular) (Clearside Biomedical pipeline, August 2020)

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