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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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