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Research programme: muscular dystrophy and metabolic disorders therapy - UMN Pharma

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Drug Profile

Research programme: muscular dystrophy and metabolic disorders therapy - UMN Pharma

Latest Information Update: 20 Jun 2011

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At a glance

  • Originator UMN Pharma
  • Developer Crucell; DSM Biologics
  • 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

Highest Development Phases

  • Discontinued Muscular dystrophies; Obesity; Type 2 diabetes mellitus

Most Recent Events

  • 20 Jun 2011 Discontinued - Preclinical for Muscular dystrophies in Japan (unspecified route)
  • 20 Jun 2011 Discontinued - Preclinical for Obesity in Japan (unspecified route)
  • 20 Jun 2011 Discontinued - Preclinical for Type-2 diabetes mellitus in Japan (unspecified route)

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