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Research programme: muscular dystrophies therapeutics - SOM Biotech/University of Minnesota

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Drug Profile

Research programme: muscular dystrophies therapeutics - SOM Biotech/University of Minnesota

Latest Information Update: 23 Jun 2022

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At a glance

  • Originator University of Minnesota
  • Developer SOM Biotech; University of Minnesota
  • Class
  • Mechanism of Action Undefined mechanism
  • 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

  • Preclinical Duchenne muscular dystrophy; Muscular dystrophies

Most Recent Events

  • 16 May 2022 SOM Biotech enters into a licensing agreement with University of Minnesota for Duchenne muscular dystrophy therapeutics
  • 16 May 2022 Preclinical trials in Duchenne muscular dystrophy in USA (unspecified route) prior to May 2022
  • 16 May 2022 Preclinical trials in Muscular dystrophies in USA (unspecified route) prior to May 2022

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