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Research programme: muscular dystropy gene therapy - 4D Molecular Therapeutics

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Drug Profile

Research programme: muscular dystropy gene therapy - 4D Molecular Therapeutics

Latest Information Update: 28 Jul 2024

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At a glance

  • Originator 4D Molecular Therapeutics
  • Class 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 Duchenne muscular dystrophy

Most Recent Events

  • 28 Jul 2024 No recent reports of development identified for research development in Duchenne muscular dystrophy in USA (IV)
  • 17 Jun 2020 Early research in Duchenne muscular dystrophy in USA (IV)

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