Research programme: Duchenne muscular dystrophy therapeutics - CombinatoRx

Drug Profile

Research programme: Duchenne muscular dystrophy therapeutics - CombinatoRx

Alternative Names: DMD therapeutics - CombinatoRx/Charley's Fund/Nash Avery Foundation

Latest Information Update: 22 Sep 2010

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At a glance

  • Originator CombinatoRx
  • Developer Zalicus
  • 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.


Highest Development Phases

  • Discontinued Muscular dystrophies

Most Recent Events

  • 15 May 2009 Early research development is ongoing in USA
  • 09 Nov 2007 Early research in Muscular dystrophy in USA (unspecified route)
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