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Research programme: inherited retinal disorders gene therapy - Oxford Biomedica/Santen Pharmaceutical

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Drug Profile

Research programme: inherited retinal disorders gene therapy - Oxford Biomedica/Santen Pharmaceutical

Alternative Names: Inherited retinal diseases gene therapy; Inherited retinal disorders therapeutics; IRD gene therapy - Oxford Biomedica/Santen Pharmaceutical; LentiViral based inherited retinal disorders gene therapy - Oxford Biomedica/Santen Pharmaceutical

Latest Information Update: 28 Jul 2024

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At a glance

  • Originator Santen Pharmaceutical
  • 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 Retinal disorders

Most Recent Events

  • 28 Jul 2024 No recent reports of development identified for preclinical development in Retinal-disorders in Japan (Ophthalmic)
  • 05 Jun 2020 Preclinical trials in Retinal disorders in Japan (Ophthalmic), prior to June 2020 (Oxford BioMedica pipeline, June 2020)

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