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Research programme: neuromuscular therapeutics - Prime Medicine

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Drug Profile

Research programme: neuromuscular therapeutics - Prime Medicine

Latest Information Update: 02 Sep 2024

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At a glance

  • Originator Prime Medicine
  • Class Gene therapies
  • Mechanism of Action Gene expression modulators; 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

  • Research Duchenne muscular dystrophy; Myotonic dystrophy; Oculopharyngeal muscular dystrophy

Most Recent Events

  • 17 Aug 2024 Early research in Duchenne muscular dystrophy in USA (Parenteral) prior to August 2024 (Prime Medicine pipeline, August 2024)
  • 17 Aug 2024 Early research in Myotonic dystrophy in USA (Parenteral) prior to August 2024 (Prime Medicine pipeline, August 2024)
  • 17 Aug 2024 Early research in Oculopharyngeal muscular dystrophy in USA (Parenteral) prior to August 2024 (Prime Medicine pipeline, August 2024)

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