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Research programme: muscular dystrophy gene therapies - Kate Therapeutics

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Drug Profile

Research programme: muscular dystrophy gene therapies - Kate Therapeutics

Latest Information Update: 05 Oct 2023

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At a glance

  • Originator Kate 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

  • Research Facioscapulohumeral muscular dystrophy; Myotonic dystrophy

Most Recent Events

  • 03 Oct 2023 Kate Therapeutics and Capsida Biotherapeutics enter into a R&D agreement to develop the drug candidates emerging from the research program gene therapies for Musclular dystrophy
  • 23 Jun 2023 Early research in Facioscapulohumeral muscular dystrophy in USA (Parenteral) (Kate Therapeutics pipeline, June 2023)
  • 23 Jun 2023 Early research in Myotonic dystrophy in USA (Parenteral) (Kate Therapeutics pipeline, June 2023)

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