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Research programme: duchenne muscular dystrophy therapeutics - Daiichi Sankyo/Orphan Disease Treatment Institute

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Drug Profile

Research programme: duchenne muscular dystrophy therapeutics - Daiichi Sankyo/Orphan Disease Treatment Institute

Alternative Names: ENA® oligonucleotides

Latest Information Update: 16 Jul 2016

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At a glance

  • Originator Daiichi Sankyo Company; Orphan Disease Treatment Institute
  • Developer Daiichi Sankyo Company
  • Class Oligonucleotides
  • 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

  • No development reported Duchenne muscular dystrophy

Most Recent Events

  • 16 Jul 2016 No recent reports of development identified for research development in Duchenne muscular dystrophy in Japan (Parenteral)
  • 14 Feb 2013 Early research in Duchenne muscular dystrophy in Japan (Parenteral)

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