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Research programme: muscular dystrophy gene therapies - Cartesian Therapeutics

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Drug Profile

Research programme: muscular dystrophy gene therapies - Cartesian Therapeutics

Alternative Names: muscular dystrophy gene therapies - Sarepta Therapeutics/Cartesian Therapeutics

Latest Information Update: 05 Dec 2023

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At a glance

  • Originator Selecta Biosciences
  • Developer Sarepta 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

  • Preclinical Duchenne muscular dystrophy; Limb girdle muscular dystrophies

Most Recent Events

  • 13 Jun 2022 Sarepta Therapeutics extends options under the Research License and Option Agreement with Selecta Biosciences for its Duchenne muscular dystrophy (DMD) and certain Limb-girdle muscular dystrophies (LGMDs) gene therapy programme
  • 30 May 2021 Preclinical trials in Duchenne muscular dystrophy in USA (Parenteral)
  • 30 May 2021 Preclinical trials in Limb girdle muscular dystrophies in USA (Parenteral)

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