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Short hairpin RNA based gene therapy - University of Connecticut/Ovid Therapeutics

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Drug Profile

Short hairpin RNA based gene therapy - University of Connecticut/Ovid Therapeutics

Alternative Names: shRNA gene therapy - Ovid Therapeutics/University of Connecticut

Latest Information Update: 28 Aug 2024

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At a glance

  • Originator Ovid Therapeutics
  • Developer Ovid Therapeutics; University of Connecticut
  • Class Gene therapies
  • Mechanism of Action Gene transference; UBE3A protein expression stimulants
  • 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
  • Available For Licensing Yes

Highest Development Phases

  • No development reported Angelman syndrome

Most Recent Events

  • 28 Aug 2024 No recent reports of development identified for research development in Angelman-syndrome in USA (Parenteral)
  • 23 Jul 2020 Ovid Therapeutics in-licenses genetic sequences for development of shRNA-based therapeutic for Angelman syndrome
  • 23 Jul 2020 Short hairpin RNA based gene therapy - University of Connecticut/Ovid Therapeutics is available for licensing as of 28 Jul 2020. https://ovidrx.com/science/partners/ (Ovid Therapeutics website, July 2020)

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