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Research programme: RNA and gene therapeutics - ReCode Therapeutics

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Drug Profile

Research programme: RNA and gene therapeutics - ReCode Therapeutics

Alternative Names: mRNA-mediated protein replacement therapies; tRNA NanoCorrector therapies

Latest Information Update: 28 Jun 2025

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At a glance

  • Originator ReCode Therapeutics
  • Class Antifibrotics; Gene therapies; RNA
  • Mechanism of Action Gene modulators; Protein replacements
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity Yes

Highest Development Phases

  • Research Cancer; Liver disorders; Neurological disorders
  • No development reported Cystic fibrosis; Primary ciliary dyskinesia

Most Recent Events

  • 28 Jun 2025 No recent reports of development identified for preclinical development in Cystic-fibrosis in USA (Inhalation)
  • 28 Apr 2024 No recent reports of development identified for preclinical development in Cystic-fibrosis in USA (IV)
  • 28 Apr 2024 No recent reports of development identified for preclinical development in Primary-ciliary-dyskinesia in USA (Inhalation)

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